| Symbol | MDT |
|---|---|
| Name | MEDTRONIC PLC |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Biotechnology: Electromedical & Electrotherapeutic Apparatus |
| Address | LOWER HATCH STREET,20 ON HATCH, DUBLIN, 2, Ireland |
| Telephone | +353 14381700 |
| Fax | — |
| — | |
| Website | https://www.medtronic.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001613103 |
| Description | One of the largest medical device companies, Medtronic develops and manufactures therapeutic medical devices for chronic diseases. Its portfolio includes pacemakers, defibrillators, heart valves, stents, insulin pumps, spinal fixation devices, neurovascular products, advanced energy, and surgical tools. The company markets its products to healthcare institutions and physicians in the United States and overseas. Foreign sales account for almost 50% of the companys total sales. Additional info from NASDAQ: |
2026-06-09 20:16
KIIL HARRY SKIP 🔴 sold 4.2K shares of Medtronic plc (MDT) at $80.45 Transaction Date: Jun 08, 2026 | Filing ID: 000008
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2026-06-08 21:07
KIIL HARRY SKIP 🔴 sold 6.8K shares of Medtronic plc (MDT) at $83.32 Transaction Date: Jun 04, 2026 | Filing ID: 000006
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2026-06-08 21:03
Director Martha Geoffrey 🔴 sold 41.9K shares of Medtronic plc (MDT) at $83.32 ($3.5M) Transaction Date: Jun 04, 2026 | Filing ID: 000006
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2026-06-08 21:02
Walter Matthew R. 🔴 sold 2.8K shares of Medtronic plc (MDT) at $83.32 Transaction Date: Jun 04, 2026 | Filing ID: 000006
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2026-06-08 21:01
Blomquist Denise L. 🔴 sold 237 shares of Medtronic plc (MDT) at $83.32 Transaction Date: Jun 05, 2026 | Filing ID: 000010
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2026-06-08 18:34
📋 KIIL HARRY SKIP (Officer) plans to sell 4K shares of Medtronic plc (at $80.44 each, total $337K) Filed: Jun 08, 2026 | ID: 004429
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2026-06-02 10:00
morph Launches the World’s First Shapeshifting Soft Robotics Cells Platform to Bring Physical AI into Real-World Applications
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2026-05-28 20:26
Walter Matthew R. 🟡 adjusted position in 700 shares (1 derivative) of Medtronic plc (MDT) Transaction Date: May 26, 2026 | Filing ID: 000004
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2026-05-28 20:26
Wall Brett A. 🟡 adjusted position in 2.7K shares (1 derivative) of Medtronic plc (MDT) Transaction Date: May 26, 2026 | Filing ID: 000002
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00604643 | Talent Aortic Cuff Stent Graft System Compassionate Use Registry | — | Abdominal Aortic Aneurysms | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00292383 | Ventricular Pacing Site Selection (V-PASS) | Phase4 | Atrioventricular Block | Unknown | — | 2008-12-01 | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00229086 | Gatekeeper European 005 | — | GERD | Terminated | — | — | ClinicalTrials.gov |
| NCT00911131 | Enhancing Detection of Small Esophageal Varices by PillCam ESO | Phase3 | Esophageal Varices | Withdrawn | — | — | ClinicalTrials.gov |
| NCT00534547 | Duodenal Exclusion for the Treatment of Type 2 Diabetes | Na | Diabetes | Withdrawn | — | — | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07401901 | Evaluation of the Safety and Effectiveness of the Novel Medtronic Experimental … | Na | Type 1 Diabetes (T1D) | Not_Yet_Recruiting | 2026-10-15 | 2028-03-29 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07575828 | Outcomes of an Optimized Workflow With PulseSelect Pulsed Field Ablation (PFA) … | Na | Paroxysmal Atrial Fibrillation (PAF) | Not_Yet_Recruiting | 2026-08-01 | 2029-03-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07644507 | Role of Intraoperative Computed Tomography in Assessment of Spine Instability i… | — | Degenerative Lumbar Spine Diseases | Not_Yet_Recruiting | 2026-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07264413 | Bleeding Reduction in Grade II-III Haemorrhoids Through Embolization Treatment | — | Hemorrhoid | Not_Yet_Recruiting | 2026-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07526896 | Advancing Clinical Heart Failure Outcomes Leveraging Defibrillation Lead Implan… | Na | Heart Failure | Not_Yet_Recruiting | 2026-08-01 | 2029-09-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07675161 | MiniMed Fit Payload Wear Pediatric Study | — | Diabetes (DM) | Not_Yet_Recruiting | 2026-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07639853 | Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Deta… | — | Arteriovenous Malformation | Not_Yet_Recruiting | 2026-07-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT07545148 | Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A M… | — | Overactive Bladder (OAB) | Not_Yet_Recruiting | 2026-07-01 | 2027-02-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07232160 | Is Density Spectral Array Display Along With Bispectral Index Superior to the D… | — | Awareness During General Anesthesia | Not_Yet_Recruiting | 2026-06-30 | 2029-12-01 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07227805 | Evaluation of the Safety and Performance of the Novel Medtronic Experimental Au… | Na | Diabetes (Insulin-requiring, Type 1 or Type 2) | Not_Yet_Recruiting | 2026-06-15 | 2027-03-17 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07600502 | Establish Whether Hyperangulated Videolaryngoscopy (HAVL) Can be Used to Facili… | Na | Intubation Skill | Not_Yet_Recruiting | 2026-06-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07234279 | Nellcor™ Investigational Device Sitting-Walking Study | — | Oxygen Saturation | Not_Yet_Recruiting | 2026-06-01 | 2026-07-01 | ClinicalTrials.gov |
| NCT07585968 | Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System … | Na | Ventricular Tachycardia | Not_Yet_Recruiting | 2026-06-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07599904 | REal-world Clinical evAulation of Medtronic NeurOVascular Products for Acute Is… | — | Acute Ischemic Stroke | Recruiting | 2026-06-01 | 2031-07-01 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07644260 | Transition From Sevoflurane to Total Intravenous Anesthesia in Pediatric Patien… | — | Anesthesia | Not_Yet_Recruiting | 2026-05-26 | 2027-03-28 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07589452 | Impact of Allometric Pacing Rate on Ventricular Diastolic Function and Cerebral… | Na | Bradycardia | Not_Yet_Recruiting | 2026-05-15 | 2028-05-31 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07602036 | Type 2 Diabetes and Pregnancy a Single-arm Interventional Study | Na | Pregnancy | Not_Yet_Recruiting | 2026-05-01 | 2029-02-01 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07547306 | Evaluation of Accelerated Bachmann Bundle Area Pacing in Heart Failure With Red… | Na | Heart Failure and Reduced Ejection Fraction | Not_Yet_Recruiting | 2026-05-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07223008 | Bilateral Embolization of the Middle Meningeal Arteries for Refractory Chronic … | Na | Migraine | Recruiting | 2026-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07507422 | Post Market Evaluation of Real World Outcomes and Durability to Support Implant… | — | Chronic Pain | Recruiting | 2026-04-17 | 2034-01-11 | ClinicalTrials.gov |
| NCT07432659 | Add-On ZIDA Sock Therapy for Overactive Bladder | Na | Overactive Bladder | Recruiting | 2026-04-17 | 2028-03-01 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07298473 | Conquer-AF Protocol for Redo Ablation Procedures in Recurrent Paroxysmal and Pe… | Na | Atrial Fibrillation (AF) | Recruiting | 2026-04-08 | 2028-03-29 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07546682 | Propel Drug-Eluting Sinus Implant Family IBUKI Cohort | — | Chronic Rhinosinusitis (CRS) | Recruiting | 2026-04-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07456865 | Post Approval Effectiveness and Durability Evaluation of the Altaviva™ Tibial D… | Na | Urge Urinary Incontinence | Recruiting | 2026-03-17 | 2032-11-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07479199 | Local Radiofrequency Ablation Plus External Beam Radiation for the Treatment of… | — | Thoracic Neoplasms | Recruiting | 2026-03-16 | 2031-03-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07384884 | Surgery and Laser Interstitial Thermal Therapy for Bilateral Glioblastomas | Na | Brain Tumours | Not_Yet_Recruiting | 2026-03-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07369310 | Comparing Biomarker-Guided DBS Programming With Standard Clinical Monopolar Pro… | Na | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2028-09-01 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07414745 | MDT-0123 Japan Study | Na | Disc Degeneration | Not_Yet_Recruiting | 2026-02-28 | 2028-03-31 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07335341 | Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectom… | — | Venous Embolism of Lower Extremities (Diagnosis) | Recruiting | 2026-02-24 | 2026-10-01 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07408141 | MiniMed Fit Payload Wear Study | — | Diabetes (Insulin-requiring, Type 1 or Type 2) | Completed | 2026-02-19 | 2026-05-14 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07287943 | To Study the Efficacy and Safety of Medtronic 780G Insulin Pump in People With … | Na | Type 1 Diabetes | Recruiting | 2026-02-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT07228117 | GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adul… | Na | Type 1 Diabetes Mellitus | Recruiting | 2026-02-02 | 2027-01-01 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT06918977 | Improving Glycemic Control With Telemedicine and Smart Insulin Pens | Na | Diabetes Mellitus | Recruiting | 2026-01-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT07305714 | Virtual Reality Educational Intervention for Nursing Students' Day Surgery Pati… | Na | Healthy | Recruiting | 2026-01-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07308847 | Horizon 360 Protocol for the Treatment of Paroxysmal Atrial Fibrillation With t… | Na | Paroxysmal AF | Recruiting | 2026-01-15 | 2027-11-22 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07356505 | Efficacy and Safety of Micra AV2 Transcatheter Pacing System | Na | AV Block Complete | Recruiting | 2026-01-12 | 2029-01-31 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07005232 | Lead Evaluation for Defibrillation and Reliability Post Approval Study | — | Tachyarrhythmia | Enrolling_By_Invitation | 2026-01-07 | 2032-09-01 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT07351071 | Post-Market Study of the Signia Circular Stapler With Tri-Staple Technology in … | Na | Colorectal Anastomosis | Recruiting | 2025-12-30 | 2027-02-28 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT06604884 | NV PSR INSPIRE-A Pipeline™ Vantage Post Approval Study | — | Intracranial Aneurysm | Recruiting | 2025-12-12 | 2033-09-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT07216976 | Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-P… | Na | Parkinson's Disease | Recruiting | 2025-11-19 | 2028-01-01 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT06584825 | Enhanced Vitals Monitoring After Major Surgery Trial | Na | Surgery | Recruiting | 2025-11-17 | 2027-12-31 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07081243 | Symplicity China Study | — | Resistant Hypertension | Recruiting | 2025-11-11 | 2031-12-30 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT07174622 | Longitudinal Real-world Clinical Outcomes Study on Symplicity Renal Denervation | — | Hypertension | Recruiting | 2025-10-28 | 2029-06-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06983470 | Predictive Utility and Mechanisms of Sacral Evoked Responses in Sacral Neuromod… | Na | Overactive Bladder | Recruiting | 2025-10-16 | 2029-10-01 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT06775886 | Effect of Personalized Accelerated Pacing in Symptomatic Patients With Non-Obst… | Na | Non-obstructive Hypertrophic Cardiomyopathy | Terminated | 2025-10-02 | 2025-10-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT07166341 | Accuracy Verification of the INVOS PM7100 | — | Tissue Oxygenation | Completed | 2025-09-29 | 2026-04-23 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT06858306 | SPHERE Per-AF Post-Approval Study | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2025-09-25 | 2030-10-01 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07115953 | Streamlined Denervation With spYral For an Optimized Treatment (SPYRAL SWYFT) i… | Na | Hypertension | Recruiting | 2025-09-22 | 2029-12-31 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07209514 | Medtronic Inceptiv™ Closed-Loop DTM Spinal Cord Stimulation for Painful Diabeti… | Na | Diabetic Peripheral Neuropathic Pain (DPN) | Enrolling_By_Invitation | 2025-09-16 | 2027-12-15 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07309133 | Local Field Potentials in Dystonia | — | Dystonia | Recruiting | 2025-09-04 | 2028-12-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07120945 | Hugo™ Robotic-Assisted Surgery (RAS) System in Gynecological Subjects (Embrace … | Na | Uterine Fibroids (UF) | Active_Not_Recruiting | 2025-08-28 | 2031-05-01 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07110922 | Angiography and Electrogram Guided Bachmann Bundle Pacing | Na | Heart Diseases | Recruiting | 2025-08-15 | 2027-12-26 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT06790147 | Stenting for Ischemic Strokes Secondary to Medically Refractory Intracranial At… | — | ICAD - Intracranial Atherosclerotic Disease | Not_Yet_Recruiting | 2025-08-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07323602 | Predicting DBS Outcomes in Dystonia Using Wearable Gait Sensors | — | Dystonia | Recruiting | 2025-08-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT07506720 | Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling | Na | Spine | Recruiting | 2025-08-01 | 2029-01-01 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT06906926 | Harmony TPV EMEA PMS | Na | Severe Pulmonary Valve Regurgitation | Recruiting | 2025-07-30 | 2032-12-31 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT07201961 | Nellcor™ Abbreviated Sensor Additional Data Collection | — | Oxygen Saturation Measurement | Completed | 2025-07-24 | 2025-08-26 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06678841 | ELEVATE-HFpEF Clinical Study | Na | Heart Failure With Preserved Ejection Fraction (HFpEF) | Recruiting | 2025-07-09 | 2029-02-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06606054 | WSO BEAT STROKE Initiative | Na | Stroke | Not_Yet_Recruiting | 2025-07-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06910059 | The CT-verified Data Collection Study to Investigate the Correlation Between th… | — | Bradycardia Sinus | Active_Not_Recruiting | 2025-06-17 | 2026-08-31 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT06710795 | AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Unde… | Na | Ventral Hernia | Active_Not_Recruiting | 2025-06-16 | 2027-05-07 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07013929 | Spyral InSight Study | Na | Hypertension | Recruiting | 2025-06-09 | 2027-07-01 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT07049003 | Deep Brain Stimulation of the Deep Cerebellar Nuclei for Refractory Tremor | Phase1 | Tremor | Recruiting | 2025-05-19 | 2028-12-31 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742801 | Onyx™ Liquid Embolic IDE Clinical Study | Na | Peripheral Arterial Hemorrhage | Recruiting | 2025-05-09 | 2027-05-01 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06907147 | SPYRAL GEMINI Pilot Study | Na | Hypertension | Recruiting | 2025-05-01 | 2029-12-22 | ClinicalTrials.gov |
| NCT06719531 | SYNERGY PLUS: Evaluation of Next Generation Sensors (NGS) and Algorithm in Pati… | Na | Type 1 Diabetes Mellitus | Withdrawn | 2025-05-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06428045 | STARLITE for Unresectable High-Grade Gliomas | Phase1 | High Grade Glioma | Recruiting | 2025-04-15 | 2030-04-30 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06922695 | Responding to AF: Pill-in-Pocket Anticoagulation Guided by Automated Monitoring… | Na | Atrial Fibrillation (AF) | Recruiting | 2025-04-14 | 2027-04-15 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT06830317 | Study on the Efficacy of Endoscopic Radiofrequency Treatment in Reducing the Ne… | — | GAVE - Gastric Antral Vascular Ectasia | Not_Yet_Recruiting | 2025-04-02 | 2027-09-02 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT07297342 | A Prospective Randomnised Controlled Trial Comparing Overall Patient Compliance… | Na | Obesity &Amp; Overweight | Recruiting | 2025-04-02 | 2027-06-01 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06411548 | InsuLearn Feasibility With Type 1 Diabetes Patients Under MDI Therapy | Na | Type 1 Diabetes Mellitus | Completed | 2025-03-27 | 2025-10-17 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06739811 | Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 202… | Na | Type I Diabetes | Recruiting | 2025-03-21 | 2026-12-01 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06732193 | Fissios© and Postoperative Complications (FPoC Trial) | Na | Surgical Procedure, Unspecified | Recruiting | 2025-03-20 | 2026-12-31 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06703489 | Safety and Performance Assessment of the Sphere-9™ Catheter and Affera™ Ablatio… | Na | Ventricular Tachycardia (VT) | Recruiting | 2025-03-18 | 2027-01-01 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638073 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Surgical Procedure, Unspecified | Recruiting | 2025-03-13 | 2026-06-20 | ClinicalTrials.gov |
| NCT06638060 | Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Co… | — | Aging | Recruiting | 2025-03-13 | 2026-06-21 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06860230 | Philips FAST Evaluation | — | Oxygen Saturation Measurement | Completed | 2025-03-11 | 2025-07-11 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06745778 | Evolution of Intracardiac Electrograms Recorded by Left Bundle Branch Pacing Le… | — | Ventricular Tachycardia (VT) | Recruiting | 2025-02-26 | 2026-07-31 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06535854 | Prevail Global Study | Na | Coronary Artery Disease | Recruiting | 2025-02-24 | 2031-02-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06777368 | REdo tranScatheter Aortic Valve Replacement for Transcatheter aOrtic Valve fail… | — | Aortic Stenosis | Recruiting | 2025-02-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06671561 | Product Surveillance Registry; Ear, Nose and Throat - EXTEND Cohort | — | Chronic Rhinosinusitis (CRS) | Withdrawn | 2025-01-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06637995 | Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort | — | Intracranial Surgery | Completed | 2025-01-27 | 2025-07-03 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT06557798 | REdo Transcatheter Aortic VALVE Implantation for the Management of Transcathete… | — | Aortic Valve Stenosis | Recruiting | 2024-12-12 | 2033-03-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07336199 | Pairing Subjective Patient Rating and DBS Programming | — | Parkinson's Disease (PD) | Recruiting | 2024-12-02 | 2026-10-01 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT07207226 | Arterial Stiffness as a Tool to Investigate Adherence in Resistant Hypertension | Na | Resistant Hypertension | Active_Not_Recruiting | 2024-11-27 | 2026-07-27 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06506903 | Avalus Ultra Post-Approval Study (PAS) | Na | Aortic Valve Disease | Active_Not_Recruiting | 2024-11-20 | 2026-11-01 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06661889 | OM2 Low Saturation Verification | — | Hypoxia | Completed | 2024-11-18 | 2025-05-27 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06690333 | Efficacy and Safety of Leadless Pacemakers Versus Left Bundle Area Pacing - A P… | Na | Pacemaker Implantation | Recruiting | 2024-11-05 | 2026-12-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06578104 | PULSED AF Post-Approval Study | — | Atrial Fibrillation | Recruiting | 2024-11-04 | 2029-06-01 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06581835 | Accuracy Performance Verification of the INVOS™ PM7100 System in Adults | — | Oxygen Saturation | Completed | 2024-10-21 | 2025-07-22 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT06676553 | INtraprocedural Feedback-Optimized Renal Denervation Based on Measurements Obta… | Phase4 | Hypertension, Uncontrolled | Recruiting | 2024-10-14 | 2028-06-30 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT05839730 | Fast Induced Remodeling in Heart Failure With Preserved Ejection Fraction | Na | Heart Failure With Preserved Ejection Fraction | Recruiting | 2024-09-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06637917 | Pulse Oximetry Performance Comparison in Newborns | — | Newborn | Completed | 2024-09-10 | 2025-09-18 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06586918 | Perfusion Index Parameter | — | Perfusion; Complications | Completed | 2024-09-04 | 2024-09-13 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06099665 | Addressing Under-treatment and Health Equity in AS and MR Using an Integrated E… | Na | Aortic Valve Stenosis | Completed | 2024-08-27 | 2025-12-01 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06540521 | Bolt CSP-M Holter Study | — | Heart Failure | Recruiting | 2024-08-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06826027 | TAV-in-SAV in Japanese Patients | — | Valve-in-valve Procedures | Active_Not_Recruiting | 2024-08-07 | 2026-03-31 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT06393920 | PulseSelect™ PFA Global Registry | — | Atrial Fibrillation | Recruiting | 2024-07-23 | 2027-07-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT02773082 | DBS for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder (OCD) | Recruiting | 2024-07-06 | 2030-01-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06449378 | Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open R… | Na | Hernia | Active_Not_Recruiting | 2024-07-02 | 2030-10-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT06188585 | Randomized Trial of UI-EWD vs. Conventional Endoscopic Therapy for Nonvariceal … | Na | Acute Gastrointestinal Bleeding | Recruiting | 2024-06-21 | 2029-09-01 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT05450393 | Data Collection of PillCamTM SB3 Capsule Endoscopy and Device-Assisted Enterosc… | — | Small Intestine Disease | Withdrawn | 2024-05-01 | 2026-04-30 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT02998229 | The Artisse™ Intrasaccular Device is Indicated for the Treatment of Wide-neck B… | Na | Intracranial Aneurysm | Recruiting | 2024-04-16 | 2032-02-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06445504 | Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable… | Na | Inguinal Hernia | Active_Not_Recruiting | 2024-04-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06286124 | Midline Restoration After HYbriD Hernia RepAir Surgery (HYDRA) | — | Incisional Hernia of Midline of Abdomen | Not_Yet_Recruiting | 2024-04-01 | 2028-04-01 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06415786 | OM2 Motion Verification Study | — | Hypoxia | Completed | 2024-03-07 | 2024-03-27 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06203054 | CLIP-IT Post-Market Study | Na | Left Atrial Appendage Exclusion | Active_Not_Recruiting | 2024-02-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT06415799 | OM2 Abbreviated Sensor Verification | — | Hypoxia | Completed | 2024-02-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT05762055 | Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOC… | Na | Cervical Radiculopathy | Enrolling_By_Invitation | 2024-02-05 | 2026-05-01 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06414564 | Effects of AHCL Insulin Pump on Glycemic Control and Psychosocial Outcomes in P… | Na | Type 1 Diabetes | Recruiting | 2024-02-01 | 2025-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06216769 | Pill-in-the-POCKET Oral Anticoagulation Strategy After AF Catheter Ablation | Na | Atrial Fibrillation | Recruiting | 2024-02-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT05510661 | Use of Export in Primary Percutaneous Coronary Intervention | Na | ST-segment Elevation Myocardial Infarction (STEMI) | Active_Not_Recruiting | 2024-01-15 | 2026-05-31 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT07632430 | End-Tidal CO2 (ETCO2) Trends in Out-of-Hospital Cardiac Arrest | — | Prehospital Resuscitation | Active_Not_Recruiting | 2024-01-01 | 2026-09-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06108973 | Evaluation of Consumption of Sevoflurane in Chronic Obstructive Pulmonary Disea… | — | Chronic Obstructive Pulmonary Disease | Unknown | 2024-01-01 | 2025-03-30 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06059638 | BradycArdia paCemaKer With AV Interval Modulation for Blood prEssure treAtmenT | Na | Hypertension | Recruiting | 2023-12-27 | 2029-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06445439 | Optimal Pacing Rate for Cardiac Resynchronization Therapy | Na | Atrial Fibrillation, Persistent | Recruiting | 2023-12-19 | 2025-08-01 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06038123 | China 3T MRI Study | Na | Bradycardia | Completed | 2023-11-28 | 2024-10-28 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT06089694 | Crome/Cobalt Respiration Study | — | Heart Failure | Completed | 2023-11-21 | 2024-06-12 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT05758662 | The Effect of Subclinical Leaflet Thrombosis and Prosthesis Type on Transcathet… | — | Aortic Valve Stenosis | Recruiting | 2023-11-16 | 2026-10-01 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06152406 | Ablate and Pace HIS Study | Na | HIS Bundle Pacing | Recruiting | 2023-10-24 | 2028-02-29 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT06096207 | DBS for Depression | Phase1 | Treatment Resistant Depression | Recruiting | 2023-10-18 | 2038-10-18 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT05870332 | Nationwide Study of Artificial Intelligence in Adenoma Detection for Colonoscopy | — | Colonic Polyp | Unknown | 2023-10-16 | 2025-05-31 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06245304 | Physiologic Pacing for Symptomatic First-Degree Heart Block | Na | Symptomatic First-degree Heart Block | Unknown | 2023-10-01 | 2025-06-30 | ClinicalTrials.gov |
| NCT06794359 | Minimally Invasive Coronary Artery Bypass Surgery in Patients With Multi Vessel… | Na | Coronary Arterial Disease (CAD) | Enrolling_By_Invitation | 2023-10-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06207838 | Transition of T1DM Patients Aged Over 65 Years Into AHCL (780G) Insulin Pump | Na | Diabetes Type 1 | Unknown | 2023-09-14 | 2024-12-31 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06048731 | Enlighten Study: The EV-ICD Post Approval Registry | — | Ventricular Arrhythmia | Active_Not_Recruiting | 2023-09-01 | 2037-10-31 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT06558474 | Optimization of Percutaenous Coronary Intervention With Liberal Use of Post-dil… | — | Coronary Artery Disease | Recruiting | 2023-09-01 | 2026-05-01 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961670 | Application of Lung Near-Infrared Spectroscopy (NIRS) in Preterm Infants | — | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT05961683 | Evaluating Pressures During Non-invasive Ventilation Utilizing NIV Plus Software | Na | Respiratory Distress Syndrome, Newborn | Unknown | 2023-08-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT04282850 | Ablation Versus Medical Management of Atrial Fibrillation in HFpEF | Na | Atrial Fibrillation | Terminated | 2023-07-10 | 2026-02-26 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05817318 | Renal Denervation in Patients With Recurrent Atrial Fibrillation After Successf… | Na | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | Terminated | 2023-06-27 | 2025-09-23 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05817409 | Predictive Factors for Succes of ITB in CP | — | Cerebral Palsy | Not_Yet_Recruiting | 2023-06-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05925985 | Propel Drug-Eluting Sinus Stent Family Open Cohort | — | Chronic Rhinosinusitis (Diagnosis) | Completed | 2023-06-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05484115 | Comparison of EVAR and ESAR for Infrarenal Aortic Aneurysms With a Wide Proxima… | Na | Aortic Aneurysm, Abdominal | Recruiting | 2023-05-26 | 2033-04-01 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05856370 | The Ailliance Post-Market Clinical Study | Na | Spinal Deformity | Recruiting | 2023-05-01 | 2031-05-01 | ClinicalTrials.gov |
| NCT05869500 | The Boston Pace Study | Na | Left Bundle Branch Area Pacing | Active_Not_Recruiting | 2023-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05775510 | Study to Evaluate Neuromodulation Subject Experience With Contemporary Spinal C… | — | Pain, Intractable | Terminated | 2023-04-25 | 2025-05-29 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05029271 | InPen User Experience | Na | Diabetes Type 1 | Completed | 2023-04-17 | 2023-12-08 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05574062 | Evaluation of the MiniMed 780 System in Paediatric Subjects | Na | Diabetes type1 | Completed | 2023-03-24 | 2024-11-15 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05766462 | Allometric-Pace Study | — | Sinus Node Dysfunction | Completed | 2023-03-20 | 2025-01-31 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05747014 | Novapak Prospective Observational Clinical Trial | — | Nasal Airway Obstruction | Completed | 2023-03-09 | 2023-12-13 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05735574 | Determining Cost of Explant of Neurmodulation Device Due to Infection | — | Neuropathic Pain | Unknown | 2023-03-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05646251 | Intra-procedural Transthoracic EChocardiogram to Facilitate Left Bundle Branch … | Na | Heart Failure | Completed | 2023-03-01 | 2024-10-27 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05714059 | Safety and Effectiveness of the MiniMed™ 780G System With DS5 CGM | Na | Type 1 Diabetes | Completed | 2023-02-28 | 2023-12-29 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05391477 | Artificial Intelligence for Diminutive Polyp Characterization | Na | Colorectal Neoplasms | Unknown | 2023-02-27 | 2024-12-01 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05652218 | REsynchronization Comparison In LBBB and Normal or Mildly Reduced VENTricular F… | Na | Left Ventricular Ejection Fraction | Active_Not_Recruiting | 2023-02-26 | 2026-09-30 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05488470 | QT Changes as Detected From LINQ ECG During Antiarrhythmic Loading (LINQ QT) | — | Atrial Arrhythmia | Completed | 2023-02-20 | 2024-07-23 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05715827 | A Prospective, Single-center, Single-arm, Pivotal Trial of the Medtronic Hugo™ … | — | Prostate Cancer | Completed | 2023-02-12 | 2023-07-10 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT05279287 | Video Analysis of Errors and Technical Performance Within Minimally Invasive Su… | — | Prostate Cancer | Unknown | 2023-02-01 | 2024-08-31 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT05378347 | Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial | Na | Abdominal Aortic Aneurysm | Recruiting | 2023-01-05 | 2031-05-01 | ClinicalTrials.gov |
| NCT06159972 | Can EndoFLIP Improve Quality of Life Before and After Fundoplication? | Na | GERD | Unknown | 2023-01-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05822895 | Review of the Impact of a Computer-aided Real-time Polyp Detection System on Ad… | — | Colonic Polyp | Recruiting | 2023-01-02 | 2031-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05541679 | Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in… | Na | Complete Heart Block | Active_Not_Recruiting | 2022-12-28 | 2025-12-31 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05672823 | Upper Extremity Versus Lower Extremity Accessory Access Sites During Transcathe… | Na | Aortic Valve Stenosis | Completed | 2022-11-28 | 2023-12-15 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05424484 | Mesh Augmented Reinforcement of Abdominal Wall Suture Line to Limit the Rate of… | Na | Incisional Hernia | Active_Not_Recruiting | 2022-11-22 | 2030-11-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT05279274 | ShorT Stay Aneurysm Repair Study | — | Abdominal Aortic Aneurysm Without Rupture | Unknown | 2022-11-01 | 2024-04-01 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT06074965 | Impact of Two Medtronic Infusion Sets on Lipohypertrophy in Type 1 Diabetes (T1… | Na | Diabetes | Completed | 2022-10-05 | 2023-05-23 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT05532670 | N600X Low Saturation Accuracy Validation | — | Hypoxia | Completed | 2022-09-29 | 2022-11-01 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT06028919 | Power Versus Temperature Controlled Ablation for Treatment of VT | Na | Ventricular Tachycardia | Completed | 2022-09-26 | 2025-11-21 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT05049720 | ExtraVascular Implantable Cardiac Defibrillator Continued Access Study | Na | Tachycardia | Withdrawn | 2022-09-01 | 2023-07-28 | ClinicalTrials.gov |
| NCT05553626 | Safety and Effectiveness of Left Bundle Branch Pacing in Patients With Cardiac … | Na | Atrioventricular Block, Second and Third Degree | Unknown | 2022-09-01 | 2025-02-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04794582 | Prevention of Incisional Hernia After Renal Transplantation | Na | Incisional Hernia | Recruiting | 2022-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05299762 | A Post Market Surveillance on INFUSE Bone Graft | — | Intervertebral Disc Degeneration | Recruiting | 2022-08-10 | 2025-08-31 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05544643 | Safety and Efficacy of Medtronic Extended Mio 30 Infusion Set | Na | Diabetes Mellitus, Type 1 | Completed | 2022-08-04 | 2022-08-04 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05198882 | Clinical Evaluation of Interstitial Laser Thermal Therapy Under Continuous MRI … | Phase1 | Drug-resistant Focal Epilepsy | Unknown | 2022-07-04 | 2024-08-15 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05366413 | Early Interventional Treatment for Cancer Pain | Na | Cancer Pain | Completed | 2022-06-02 | 2024-10-26 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT05199194 | Randomization to Endovascular Treatment Alone or Preceded by Systemic Thromboly… | Phase3 | Stroke, Ischemic | Recruiting | 2022-05-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT04391803 | EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysm… | Na | Intracranial Aneurysm | Terminated | 2022-05-06 | 2025-10-20 | ClinicalTrials.gov |
| NCT05307965 | RETRIEVE-AMI Study | Na | Myocardial Infarction | Completed | 2022-05-06 | 2025-05-28 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05325294 | Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults an… | Na | Type 1 Diabetes | Completed | 2022-05-05 | 2024-01-03 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05349695 | Patient Profiling and Outcome Assessment in Spinal Cord Stimulation for Chronic… | — | Failed Back Surgery Syndrome | Unknown | 2022-05-01 | 2024-05-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05227053 | STOP AF First Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Recruiting | 2022-04-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT05149755 | Evolut™ EXPAND TAVR II Pivotal Trial | Na | Moderate Aortic Valve Stenosis | Active_Not_Recruiting | 2022-04-27 | 2034-12-01 | ClinicalTrials.gov |
| NCT05455554 | The Use of FlowMet-R Technology to Predict Wound Healing in CLI Patients in a W… | — | Critical Limb Ischemia | Unknown | 2022-04-27 | 2023-09-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT04964765 | The Basel CardioInsightTM - 3D Mapping Study | — | New-onset Atrial Fibrillation (NOAF) | Recruiting | 2022-04-12 | 2028-12-01 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT06094114 | Evaluation of VDD Leadless Pacing System During Exercise | — | Bradycardia | Completed | 2022-04-01 | 2022-12-31 | ClinicalTrials.gov |
| NCT05105360 | Prevention of Petersen's Hernia After Laparoscopic Gastrectomy | Na | Petersen's Hernia | Active_Not_Recruiting | 2022-04-01 | 2029-01-26 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05811988 | Cost Assessment of Videolaryngoscopy Compared to Direct Laryncoscopy in a Large… | — | Economic Problems | Completed | 2022-03-31 | 2022-06-15 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05340361 | Efficacy and Safety of Zotarolimus-eluting Stent Overexpansion With OCT | — | Coronary Artery Disease | Active_Not_Recruiting | 2022-03-23 | 2026-12-31 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT05224258 | Evaluation of the MiniMed™ 780G System in Type 1 Adult and Pediatric Subjects U… | Na | Type 1 Diabetes | Completed | 2022-03-17 | 2024-06-21 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT06239454 | Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease | Na | Parkinson's Disease | Unknown | 2022-03-01 | 2025-02-28 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05230524 | DIAMOND AF Post-Approval Study | — | Paroxysmal Atrial Fibrillation | Terminated | 2022-02-28 | 2025-12-17 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT05238142 | In-Home Study With MiniMed™ 780G Pump Automated Control in Type 2-Evaluation of… | Na | Type 2 Diabetes Treated With Insulin | Completed | 2022-02-25 | 2025-01-11 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT06847295 | Epidural Electrical Stimulation to Restore Standing and Walking in Patients Wit… | Na | Spinal Cord Injuries (SCI) | Recruiting | 2022-01-28 | 2027-01-10 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT05200923 | Pelvic Health Electrically Evoked Recording (PEER) 2 Study | Na | Overactive Bladder | Recruiting | 2022-01-18 | 2026-12-18 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT06031051 | Capsule Endoscopy as an Alternative to Colonoscopy | Na | Colonic Disease | Unknown | 2021-12-22 | 2024-12-01 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05294445 | From the Emergency Department Directly to Ablation of Atrial Fibrillation Study | Na | Atrial Fibrillation (AF) | Active_Not_Recruiting | 2021-12-15 | 2028-12-14 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT05029414 | EnDovascular Therapy Plus Best Medical Treatment (BMT) Versus BMT Alone for Med… | Na | Acute Ischemic Stroke | Active_Not_Recruiting | 2021-12-09 | 2025-06-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT04282161 | Pivotal Study of the Medtronic Axys EX Rotational Atherectomy System | Na | Peripheral Arterial Disease | Withdrawn | 2021-12-01 | 2024-02-01 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT05177354 | Medtronic Closed-Loop Spinal Cord Stimulation System | Na | Low Back Pain | Completed | 2021-11-30 | 2025-07-28 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT07106242 | Adaptive Deep Brain Stimulation (aDBS) Study (Early Adapter) Part II | Na | Parkinson Disease | Completed | 2021-11-29 | 2023-10-23 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT04825847 | Neurocognitive Disorders After Major Surgery in Elderly | Na | Anesthesia | Recruiting | 2021-11-24 | 2025-08-01 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05075590 | Coronary Access After Supra-Annular THV Implantation | Na | Coronary Angiography | Unknown | 2021-10-27 | 2024-07-31 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05077774 | Harmony TPV Post-Approval Study | Na | Congenital Heart Disease | Active_Not_Recruiting | 2021-10-25 | 2035-03-01 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05198674 | SPYRAL AFFIRM Global Study of RDN With the Symplicity Spyral RDN System in Subj… | Na | Hypertension | Active_Not_Recruiting | 2021-10-20 | 2029-11-30 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05115214 | Safety and Performance of the Affera SpherePVI™ Multi-Ablation System to Treat … | Na | Atrial Fibrillation | Recruiting | 2021-10-19 | 2027-10-15 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT05022719 | Technical Feasibility Evaluation of Mucosal Staining During Colon Capsule Endos… | Na | Colorectal Cancer | Completed | 2021-10-04 | 2022-09-28 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT03907982 | Investigation of Therapeutic Ablation Versus Cardioversion for AF | Na | Persistent Atrial Fibrillation | Completed | 2021-10-01 | 2023-04-26 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05116332 | Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gyna… | — | Surgery | Completed | 2021-09-11 | 2023-03-10 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05023772 | Laser Interstitial Thermal Ablation and Stereotactic Radiosurgery for Patients … | Na | Neoplasm Metastasis | Recruiting | 2021-09-02 | 2028-06-20 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005962 | Prospective Registry for Assessment of Acute Ischemic Stroke Patients Treated W… | — | Acute Ischemic Stroke | Completed | 2021-08-30 | 2024-05-21 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT05005949 | STOP Persistent AF PAS | — | Persistent Atrial Fibrillation | Active_Not_Recruiting | 2021-08-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04765046 | The Influence of Age on EEG Signals and Consciousness During Anesthesia | Na | Anesthesia | Completed | 2021-08-18 | 2023-04-03 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT04929678 | Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis | Na | Juvenile Idiopathic Scoliosis | Terminated | 2021-08-12 | 2026-01-14 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT05095935 | Medtronic Signia SDR Product Surveillance Registry | — | Minimally Invasive Surgical Procedures | Completed | 2021-08-10 | 2024-10-01 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT04964817 | HFpEF and Symptomatic Obstructive Iliofemoral Venous Disease Study | — | Heart Failure With Preserved Ejection Fraction | Terminated | 2021-08-03 | 2023-04-12 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT05144503 | Safety and Performance of the SpherePVI™ Catheter to Treat Paroxysmal Atrial Fi… | Na | Atrial Fibrillation | Recruiting | 2021-07-22 | 2027-10-15 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04901143 | Meal Handling of Advanced Closed Loop Insulin Delivery. | Na | Type 1 Diabetes | Completed | 2021-07-17 | 2022-01-01 | ClinicalTrials.gov |
| NCT04982588 | Evolut PRO China Clinical Study | Na | Severe, Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-07-17 | 2028-05-15 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04804332 | Removal of Intrauterine Retained Products of Conception (RPOC) After Miscarriag… | Na | Retained Products of Conception | Recruiting | 2021-07-12 | 2027-12-30 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04810481 | Bispectral Index and End-Tidal Anesthetic Gas Concentration in Pediatric Patien… | Na | Anesthesia | Completed | 2021-07-02 | 2022-10-12 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04806516 | Phase II Adaptive Deep Brain Stimulation for Obsessive-Compulsive Disorder | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2021-07-01 | 2026-07-30 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04853108 | Remote Monitoring of COVID-19 Positive Outpatients | — | Covid19 | Terminated | 2021-06-25 | 2023-04-01 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04926857 | DEFINE AFib (Atrial Fibrillation) | — | Atrial Fibrillation | Terminated | 2021-06-21 | 2024-01-25 | ClinicalTrials.gov |
| NCT04863664 | Lead EvaluAtion for Defibrillation and Reliability (LEADR) / Lead Evaluation fo… | Na | Tachyarrhythmia | Completed | 2021-06-21 | 2025-11-06 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04320849 | Human Use Condition Study- Evaluation of Implanted Leads in Humans | — | Pacemaker Malfunction | Completed | 2021-06-01 | 2022-05-23 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04639258 | Medtronic Evolut™ EXPAND TAVR I Feasibility Study | Na | Aortic Valve Stenosis | Terminated | 2021-05-28 | 2022-06-07 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04503395 | ShOrt neCK AAA RAndomized Trial - ESAR and FEVAR: SOCRATES | Na | Aortic Aneurysm, Abdominal | Recruiting | 2021-05-21 | 2032-06-01 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04873271 | Evaluation of Implantable Tibial Neuromodulation (TITAN 1) Feasibility Study | Na | Overactive Bladder | Completed | 2021-05-11 | 2022-07-08 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04833712 | Stereotactic Radioablation for the Treatment of Refractory Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2021-05-10 | 2022-08-30 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04854200 | HVAD(TM) SMART 1.0 Study | — | Chronic Heart Failure | Withdrawn | 2021-05-01 | 2025-08-22 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04894838 | DIStal gastriC Bypass OUtcome in Revision SurgEry After Roux-en-y Gastric Bypass | Na | Obesity, Morbid | Recruiting | 2021-05-01 | 2029-12-01 | ClinicalTrials.gov |
| NCT04595487 | LVSP vs RVP in Patients With AV Conduction Disorders | Na | Cardiac Pacing | Recruiting | 2021-05-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04735016 | DiamondTemp Global Registry | — | Arrhythmia | Active_Not_Recruiting | 2021-04-22 | 2031-03-01 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04118530 | Long Term Arrhythmia Risk and Cardiovascular Events in Hematopoietic Stem Cell … | — | Hematopoietic Stem Cell Transplant | Completed | 2021-04-21 | 2024-06-17 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04484220 | Ellipsys Vascular Access System Post Market Surveillance (PS) Study | Na | Renal Disease, End Stage | Completed | 2021-04-13 | 2025-03-31 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04809285 | Use of the Guardian™ Connect System With Smart Connected Devices | Na | Type 1 Diabetes Mellitus | Completed | 2021-04-06 | 2023-09-29 | ClinicalTrials.gov |
| NCT04811963 | SpO2 Accuracy Low Saturation Validation of the OxySoftN Sensor | — | Hypoxia | Completed | 2021-04-06 | 2021-04-09 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04722250 | SMall Annuli Randomized To Evolut™ or SAPIEN™ Trial | Na | Symptomatic Aortic Stenosis | Active_Not_Recruiting | 2021-04-02 | 2027-12-01 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04726150 | Effect of CoVid-19 (CoronaVirusDisease-19) and Exercise on Myocardial Fibrosis … | — | Covid19 | Completed | 2021-04-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT04673136 | Usefulness of GI-GENIUS in FIT-based Colorectal Cancer Screening Program. | Na | Colorectal Neoplasms | Completed | 2021-04-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT03811405 | Physiology, Imaging and Modeling of Essential Tremor | Na | Essential Tremor | Completed | 2021-04-01 | 2025-06-01 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04723758 | COLO-DETECT: Can an Artificial Intelligence Device Increase Detection of Polyps… | Na | Colonic Polyp | Completed | 2021-03-29 | 2023-04-20 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04881136 | Frailty and Falls Implantable System for Prediction and Prevention | Na | Fall Patients | Unknown | 2021-03-23 | 2022-06-30 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04823312 | Evaluation of Medtronic DUO Extended Set | Na | Diabetes Mellitus, Type 1 | Unknown | 2021-03-18 | 2021-11-01 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04757142 | PLASMA Chile (PLASMA Chile) | — | Heart Failure | Completed | 2021-03-11 | 2024-11-12 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT04904224 | Diagnosis of Inflammatory Bowel Disease by Examining the Entire Bowel by Pan-in… | Na | Inflammatory Bowel Diseases | Unknown | 2021-03-07 | 2023-03-31 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT05884593 | Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System | Na | Spinal Deformity | Active_Not_Recruiting | 2021-03-05 | 2025-12-30 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04810780 | Safety and Efficacy of DUO Extended Set: Combined Glucose Sensor and Infusion S… | Na | Type 1 Diabetes | Completed | 2021-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT04776811 | Evaluation of Accuracy of Guardian Sensor 3 in Diabetes Patients on Peritoneal … | — | Diabetes Mellitus (Diagnosis) | Completed | 2021-03-01 | 2022-09-30 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04765735 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Algo… | Na | Chronic Pain | Completed | 2021-02-23 | 2021-06-29 | ClinicalTrials.gov |
| NCT04546555 | Physiologic Accelerated Pacing as a Treatment in Patients With Heart Failure Wi… | Na | Heart Failure, Diastolic | Completed | 2021-02-23 | 2023-05-25 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04597307 | IN.PACT™ Quality of Life Post-Reimbursement Study | — | Obstructive Disease | Unknown | 2021-02-17 | 2024-12-01 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04308291 | The MiniMed™ 780G Glycemic Control and Quality of Life Study for the Treatment … | — | Type 1 Diabetes | Completed | 2021-02-15 | 2022-10-27 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04602546 | Evaluation of Bispectral Index (BIS™) and Levels of Sedation With Common Inhala… | Na | Anesthesia | Completed | 2021-02-09 | 2022-08-26 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04671888 | Chronic Obstructive Pulmonary Disease (COPD) Monitoring | Na | COPD | Unknown | 2021-02-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04725838 | Differential Target Multiplexed Spinal Cord Stimulation (DTM-SCS®) Real World O… | — | Chronic Pain | Completed | 2021-01-29 | 2023-07-01 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04583709 | ECG Belt to Assess Electrical Synchronization | Na | Bradycardia | Completed | 2021-01-13 | 2021-06-25 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04416659 | Flow Arrest Safety and Technical Success With Balloon Guide Catheters | — | Acute Ischemic Stroke | Completed | 2021-01-12 | 2021-10-27 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT04124263 | Use of Short Text Messages to Promote Medication Adherence in Hypertensive Pati… | Na | Hypertension | Completed | 2021-01-07 | 2022-11-10 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT02347111 | Pharmacogenetic Study of Antiarrhythmic Drugs for Atrial Fibrillation | Phase4 | Atrial Fibrillation | Recruiting | 2020-12-31 | 2026-06-30 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04408846 | Minimally Invasive Surgery Versus Traditional Open Surgery In The Treatment Of … | Na | Intervertebral Disc Degeneration | Withdrawn | 2020-12-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04159454 | PITA-HF: Feasibility, Safety, and Tolerability | Na | Heart Failure | Completed | 2020-11-20 | 2023-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT04543539 | IN.PACT™ AV Access Post-Approval Study (PAS002) | — | Arteriovenous Fistula | Active_Not_Recruiting | 2020-11-13 | 2029-02-01 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT04601454 | DTM (TM) Spinal Cord Stimulation (SCS) Study | Na | Chronic Pain | Completed | 2020-11-05 | 2022-08-25 | ClinicalTrials.gov |
| NCT05181098 | Prospective Robotic-Guided Registry of Spine Surgery | — | Spinal Disease | Unknown | 2020-11-05 | 2024-12-31 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04310839 | Outpatient Left Laparoscopic Colectomy | — | Colonic Neoplasms | Completed | 2020-11-03 | 2022-12-02 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04616391 | AHCL System Initiation in T1D Patients naïve to Technology | Na | Diabetes Mellitus, Type 1 | Unknown | 2020-11-02 | 2021-07-01 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04663295 | MiniMed™ 670G System China Study for Type I Diabetic | Na | Diabetes Mellitus, Type 1 | Completed | 2020-10-31 | 2021-06-22 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04402632 | Embolization of the Middle Meningeal Artery With ONYX™ Liquid Embolic System fo… | Na | Subdural Hematoma | Completed | 2020-10-27 | 2025-04-03 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04433065 | TTVR Early Feasibility Study | Na | Tricuspid Regurgitation | Recruiting | 2020-10-20 | 2031-07-30 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04009512 | Endovascular Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Active_Not_Recruiting | 2020-10-06 | 2026-08-26 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04304963 | Hypo-METRICS: Hypoglycaemia - Measurement, ThResholds and ImpaCtS | — | Diabetes Mellitus, Type 1 | Completed | 2020-10-01 | 2022-10-31 | ClinicalTrials.gov |
| NCT04778826 | Immune Response Following Lobectomy Along With or Without Bilateral Transcervic… | Na | Lung Neoplasm Malignant | Unknown | 2020-10-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT04578340 | Long Term Outcomes Following Hernia Repair With Mesh | — | Abdominal Hernia | Recruiting | 2020-10-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04450628 | Esophagogastric Junction Distensibility During Hiatal Hernia Repair | Na | Esophagogastric Junction Distensibility | Active_Not_Recruiting | 2020-09-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506684 | Reveal LINQ Respiration Clinical Study | — | Respiratory Rate | Completed | 2020-09-25 | 2021-07-31 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04506866 | InterStim Micro Post Market Clinical Follow-up Study (ELITE) | Na | Overactive Bladder | Terminated | 2020-08-25 | 2023-12-08 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04559763 | SpO2 Accuracy Validation of the OxySoft Sensor Via Reference CO-Oximetry Motion… | — | Hypoxia | Completed | 2020-08-18 | 2020-08-21 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04466384 | Bispectral Index and Levels of Sedation With Propofol With/Without Remifentanil… | Na | Anesthesia | Completed | 2020-08-11 | 2021-03-03 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04539145 | CHOCO-CABANA Trial | Phase4 | Atherosclerosis | Unknown | 2020-08-04 | 2022-03-27 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT03833323 | Implantable System for Remodulin Post-Approval Study | — | Pulmonary Arterial Hypertension | Withdrawn | 2020-08-01 | 2021-06-30 | ClinicalTrials.gov |
| NCT04489225 | Personalized Therapy Study - HFRS (TriageHF) Post Approval Study | — | Heart Failure | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT04496518 | Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Stu… | — | Ventricular Tachycardia | Active_Not_Recruiting | 2020-08-01 | 2028-01-31 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT06442410 | Comparison of DTM™ SCS Therapy Combined With Conventional Medical Management (C… | Na | Pain, Intractable | Completed | 2020-07-24 | 2023-10-17 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04203823 | Feasibility Studies of Personalized Closed Loop | Na | Type 1 Diabetes | Completed | 2020-07-20 | 2022-01-27 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04269668 | An Open-label, Two-center, Randomized, Cross-over Study to Evaluate the Safety … | Na | Diabetes Mellitus, Type 1 | Completed | 2020-07-19 | 2021-03-20 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04479826 | Unannounced Meal Handling of Advanced Closed Loop Insulin Delivery in Monitored… | Na | type1diabetes | Completed | 2020-07-16 | 2021-07-16 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04489095 | Conduction Disease After Transcatheter Aortic Valve Replacement | Na | Aortic Stenosis | Completed | 2020-07-16 | 2022-08-01 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04436822 | Evaluation of Updated Continuous Glucose Monitoring (CGM) Form Factor in Adults… | Na | Type 1 Diabetes Mellitus | Completed | 2020-07-15 | 2022-04-12 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04420728 | Closed-Loop Insulin in Mothers With Type 1 Diabetes and Baby Feeding Practices | Na | Diabetes Mellitus Type 1 Pre-Existing | Completed | 2020-07-15 | 2023-02-28 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04233034 | Hybrid Closed Loop Therapy and Verapamil for Beta Cell Preservation in New Onse… | Phase3 | Type1 Diabetes | Completed | 2020-07-09 | 2022-09-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04496544 | Safety Assessment of Femoropopliteal Endovascular Treatment With PAclitaxel-coa… | — | Peripheral Arterial Disease | Completed | 2020-07-01 | 2024-06-30 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04267055 | DISSECT-N Post Market Data Collection Registry | — | Thoracic Aortic Dissection | Completed | 2020-06-25 | 2024-07-05 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04552275 | The HALT Biomarker Study | Phase1 | Aortic Stenosis | Recruiting | 2020-06-22 | 2035-06-22 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04782986 | Pan-intestinal Capsule Endoscopy Versus Colonoscopy in Iron Deficiency Anemia o… | Na | Iron Deficiency Anemia | Completed | 2020-06-19 | 2023-01-31 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04311086 | SPYRAL DYSTAL Renal Denervation Global Clinical Study | Na | Hypertension | Completed | 2020-06-12 | 2022-12-22 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04657783 | French National Cohort of People With Type 1 Diabetes | — | Diabetes Mellitus, Type 1 | Recruiting | 2020-06-10 | 2035-06-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04245345 | Accelerometer Sensing for Micra AV Study | Na | AV Block | Completed | 2020-06-09 | 2022-01-10 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04058860 | Study of Microcirculation During Extracorporeal Circulation in Cardiac Surgery | Na | Heart Diseases | Completed | 2020-06-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04250194 | Navigation Endoscopy to Reach Indeterminate Lung Nodules Versus Trans-Thoracic … | Na | Lung Nodule | Completed | 2020-05-22 | 2024-07-02 | ClinicalTrials.gov |
| NCT04375891 | Radiation Therapy Alone Versus Radiation Therapy Plus Radiofrequency Ablation (… | Na | Oncology | Active_Not_Recruiting | 2020-05-22 | 2027-07-01 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT04378114 | Impact of Acetaminophen on Performance of Guardian™ Sensor (3) in Adults | Na | Type 1 Diabetes Mellitus | Completed | 2020-05-18 | 2020-07-17 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03405740 | Virtual E-health System for Implantable Cardioverter Defibrillators | Na | Cardiac Arrhythmia | Active_Not_Recruiting | 2020-05-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT05150041 | The Efficacy of Guardian Connect to Modify Lifestyle in Patients With Type 2 Di… | Na | Diabetes Mellitus, Type 2 | Completed | 2020-04-07 | 2021-12-07 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03873714 | Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked I… | Na | Intracranial Aneurysm | Terminated | 2020-04-02 | 2023-09-18 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT03900468 | Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study… | Na | Epilepsy | Terminated | 2020-03-05 | 2026-02-26 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04096248 | CT (Computerized Tomography) for Late EndovasculAr Reperfusion | — | Stroke, Cardiovascular | Completed | 2020-02-15 | 2022-05-01 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04253184 | Micra AV Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Completed | 2020-02-08 | 2026-01-14 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04235491 | Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pace… | — | Bradycardia | Active_Not_Recruiting | 2020-02-06 | 2029-06-01 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT04206501 | OptiVol for Precision Medical Management of Heart Failure | Na | Ischemic and Non-ischemic Cardiomyopathy | Terminated | 2020-02-05 | 2022-11-20 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT03820947 | VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial | Na | Venous Reflux | Terminated | 2020-02-05 | 2025-11-10 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04244513 | Deep Brain Stimulation Treatment for Chorea in Huntington's Disease | Na | Huntington Disease | Unknown | 2020-02-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT04471181 | Greek Study for Endovascular Repair of Ruptured Abdominal Aortic Aneuryms | — | Rupture, Aortic | Unknown | 2020-02-01 | 2023-02-01 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04214899 | PLASMA Mexico (PLASMA Mexico) | — | Heart Failure | Completed | 2020-01-30 | 2024-11-25 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04180696 | Mid-Q Response Study | Na | Heart Failure | Completed | 2020-01-23 | 2024-03-28 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04272762 | A Randomized Sham-controlled Study of Pulmonary Vein Isolation in Symptomatic A… | Na | Atrial Fibrillation | Completed | 2020-01-23 | 2024-03-04 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT04494035 | AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System | Na | Arteriovenous Graft Thrombosis | Terminated | 2020-01-14 | 2020-10-23 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06874465 | Transcatheter Aortic Valve Implantation Registry at the National Research Cente… | Na | Aortic Valve Stenosis | Recruiting | 2020-01-10 | 2026-01-10 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT06924957 | Influence of Body Position on the Defecation Model During Anorectal Manometry. | — | Constipation | Enrolling_By_Invitation | 2020-01-10 | 2025-12-01 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04241328 | Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery | — | Cardiovascular Diseases | Recruiting | 2020-01-09 | 2026-12-31 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04172116 | Continuous Glucose Monitoring (CGM) After Surgical Variations of the Roux-en-y … | — | Continuous Glucose Monitoring | Unknown | 2020-01-01 | 2021-01-01 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04212780 | Dual Lead Thalamic Deep Brain Recording (DBR)-DBS Interface for Closed Loop Con… | Na | Essential Tremor | Recruiting | 2019-12-24 | 2029-12-31 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04073563 | Transforaminal Lumbar Interbody Fusion (TLIF) | Na | Degenerative Disease of the Lumbosacral Spine | Active_Not_Recruiting | 2019-12-19 | 2028-07-01 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04198701 | Pulsed Field Ablation to Irreversibly Electroporate Tissue and Treat AF | Na | Atrial Fibrillation | Completed | 2019-12-10 | 2022-11-28 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04120610 | FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease… | — | Peripheral Artery Disease | Terminated | 2019-12-09 | 2022-11-21 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04073420 | Medtronic Cardiac Surgery PMCF Registry | — | Valve Disease, Heart | Recruiting | 2019-12-02 | 2039-12-31 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT04016324 | InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study | Na | Overactive Bladder | Completed | 2019-11-28 | 2020-10-09 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT03938142 | Goalsetting in Patients With Chronic Pain: a European Survey | — | Chronic Pain | Completed | 2019-11-23 | 2020-05-27 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04157205 | Prospective Evaluation Of Exercise-Induced Cardiac Conduction Instability In Pr… | Na | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04112290 | A Prospective Incident Study of Arrhythmias in Hypertrophic Cardiomyopathy | — | Hypertrophic Cardiomyopathy | Active_Not_Recruiting | 2019-11-05 | 2027-12-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT04146168 | Lake Washington Vascular VenaSeal™ Post-Market Evaluation | — | Varicose Veins | Unknown | 2019-11-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT06499220 | Electrically Evoked Compound Action Potentials Human Observation Medtronic Syst… | Na | Chronic Pain | Completed | 2019-10-30 | 2023-10-16 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04106479 | NIRS in Congenital Heart Defects - Correlation With Echocardiography | — | Congenital Heart Defect | Recruiting | 2019-10-11 | 2025-12-01 | ClinicalTrials.gov |
| NCT04281134 | Development of Adaptive Deep Brain Stimulation for OCD | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2019-10-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04285918 | Evaluation of Prevalence and Clinical Impact of Atrial Fibrillation in Elderly … | — | Cryptogenic Stroke | Unknown | 2019-10-02 | 2024-10-02 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT04172883 | Management of Device Detected AT and Impact of Device Treatment Algorithms on A… | Na | Cardiovascular Diseases | Terminated | 2019-10-01 | 2021-07-28 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT03489096 | Cryoballoon Targeting Atrial Fibrosis in Atrial Fibrillation | Na | Atrial Fibrillation | Withdrawn | 2019-10-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT03950492 | Feasibility of Deep Brain Stimulation as a Novel Treatment for Refractory Opioi… | Na | Opioid-Related Disorders | Active_Not_Recruiting | 2019-09-30 | 2026-12-31 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04603547 | Transcutaneous Carbon Dioxide Monitoring in Neonates Receiving Therapeutic Hypo… | — | Neonatal Encephalopathy | Active_Not_Recruiting | 2019-09-28 | 2027-12-30 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT04119323 | Image Location and Performance of Left Bundle Branch Pacing | — | Cardiac Pacing | Completed | 2019-09-24 | 2020-07-14 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT03912662 | ProGripTM Self-Gripping Polyester Mesh in Incisional Hernia Prevention | Na | Incisional Hernia | Terminated | 2019-09-18 | 2022-09-12 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT04091048 | Optimize PRO Study | — | Symptomatic Aortic Stenosis | Completed | 2019-09-16 | 2024-11-13 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT03859167 | Study of the Loss of AV Synchrony at Maximum Exercise | — | Exercise | Terminated | 2019-09-10 | 2023-04-10 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT04177199 | What is the Workload Burden Associated With Using the Triage HF+ Care Pathway? | — | Heart Failure | Unknown | 2019-09-06 | 2025-06-30 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT03775980 | CIRSE Emprint Microwave Ablation Registry | — | Colorectal Neoplasms Malignant | Completed | 2019-09-04 | 2026-01-31 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04056520 | Clinical and Radiological Outcomes of Posterior Cervical Fusion with Medtronic … | — | Degenerative Disc Disease | Completed | 2019-09-01 | 2024-12-13 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04041583 | Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented Wi… | — | Cervical Fusion | Recruiting | 2019-09-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT04011371 | Cyanoacrylate Closure for Treatment of Venous Leg Ulcers | Na | Venous Leg Ulcer | Completed | 2019-09-01 | 2022-06-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04120909 | MARC-2: MARKERS AND RESPONSE TO CRT in Non-LBBB | — | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | Unknown | 2019-08-26 | 2022-08-01 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04056390 | Ablation STrategies for Repeat PrOcedures in Patients With Atrial Fibrillation … | Na | Atrial Fibrillation | Unknown | 2019-08-01 | 2025-02-15 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT04020822 | Feasibility Study of New Subcutaneous Glucose Sensor With Recording Devices | Na | Type 1 Diabetes | Completed | 2019-07-29 | 2019-08-27 | ClinicalTrials.gov |
| NCT03948880 | Incidence OIRD Medical and Trauma Patients | — | Respiratory Depression | Unknown | 2019-07-29 | 2019-11-29 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03959423 | Safety Evaluation of the Advanced Hybrid Closed Loop (AHCL) System | Na | Type 1 Diabetes Mellitus | Completed | 2019-07-24 | 2023-10-27 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03831724 | Definition and Validation of Normative Data of EndoFLIP™ Measurements in Health… | Na | Healthy Subjects | Withdrawn | 2019-07-01 | 2020-05-01 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT03458390 | Use of a Colon Irrigation Device as a Preparation for a Colon Visualization Pro… | Na | Screening Colonoscopy | Completed | 2019-06-27 | 2020-01-19 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04068233 | Impact of Pacing Mode and Diastolic Function on Cardiac Output | Na | Diastolic Function | Completed | 2019-06-26 | 2020-02-05 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT03966911 | Performance Evaluation of an Advanced Algorithm With CGM in Adults, Adolescents… | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT04006184 | Retrospective Review of Saphenous Vein Incompetence: Venaseal Versus Endovenous… | — | Varicose Veins | Completed | 2019-06-14 | 2019-08-30 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03775694 | Diffusion MRI-1 Imaging Database | — | Epilepsy | Completed | 2019-06-06 | 2022-04-29 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03040414 | Fuzzy Logic Automated Insulin Regulation | Na | Type 1 Diabetes Mellitus | Completed | 2019-06-03 | 2020-04-20 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03869645 | CAPERE Thrombectomy System Post-Market Clinical Follow Up Study | — | Observational Study | Terminated | 2019-06-01 | 2020-08-26 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT03941275 | SelectSecure 3830 Lead Imaging | — | Heart Diseases | Completed | 2019-05-24 | 2021-11-15 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT04073576 | Assessment of Two Insulin Pump Insulin Delivery Systems in Type 1 Diabetes. | Na | Type1diabetes | Unknown | 2019-05-20 | 2019-10-11 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03797144 | Fenestrated Screw Study | Na | Degenerative Spinal Disease | Terminated | 2019-04-18 | 2020-07-15 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03706677 | FIRE AND ICE II Trial Pilot | Na | Persistent Atrial Fibrillation | Completed | 2019-04-05 | 2023-04-06 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03889613 | Pillcam Crohn's Capsule for Monitoring of Panenteric Mucosal Healing in Crohn's… | Na | Crohn Disease | Unknown | 2019-04-03 | 2024-11-01 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03814564 | ASSESSment of Perfusion, Oxygen Saturation, Endothelial Function and Coagulatio… | — | Circulatory Failure | Completed | 2019-04-01 | 2023-10-31 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT03955432 | Long-term Cardiac Monitoring in Epilepsy | Na | Focal Epilepsy | Terminated | 2019-03-19 | 2023-01-03 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT04075500 | Optimal Detection of Atrial Fibrillation in TIA | Na | Atrial Fibrillation | Completed | 2019-03-12 | 2025-08-31 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03710083 | A Pivotal Study to Evaluate Guardian™ Connect CGM System Performance in China | Na | Diabetes Mellitus | Completed | 2019-02-28 | 2019-07-25 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03569111 | Clinical Description of a Bronchoscopic Approach to Ablate Lung Nodules Using t… | — | Cancer, Lung | Completed | 2019-02-27 | 2020-10-28 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03854279 | Comparison of Bizact With Electroscissor for Tonsillectomy | Phase4 | Tonsillar Hypertrophy, Tonsillitis | Unknown | 2019-02-20 | 2020-12-31 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03776825 | Permacol Paste in Perianal Crohn's Disease | — | Crohn Disease | Unknown | 2019-02-07 | 2021-10-01 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03752151 | Micra Atrial TRacking Using A Ventricular AccELerometer 2 | Na | Atrioventricular Conduction Block | Completed | 2019-01-22 | 2019-08-07 | ClinicalTrials.gov |
| NCT03515811 | A Post Market Study to Confirm the Safety and Performance of the Signia™ Stapli… | — | Abdominal Injury | Completed | 2019-01-22 | 2020-07-13 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03946618 | Neurophysiologically Based Brain State Tracking and Modulation in Focal Epilepsy | Na | Epilepsy | Active_Not_Recruiting | 2019-01-18 | 2027-02-01 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03697980 | Apogee, A HeartWare HVAD Destination Product Surveillance Registry (PSR) Platfo… | — | Chronic Heart Failure | Completed | 2019-01-17 | 2022-02-10 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT03761277 | Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternati… | Phase4 | Chronic Non-malignant Pain | Completed | 2019-01-16 | 2021-12-06 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04016285 | Total Knee Replacement With Tourniquet or Aquamantys | Na | Knee Replacement | Completed | 2019-01-15 | 2023-04-18 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT04023890 | Ventricular Electrical Synchronization by Stimulating Left and Right Bundle Bra… | — | Cardiac Pacing | Completed | 2019-01-14 | 2020-01-31 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03835039 | The Ability of NIRS to Predict Brain Injury in Hypoxic Ischemic Encephalopathy | — | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | Terminated | 2019-01-03 | 2022-01-01 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT03738124 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Thoracic Aort… | Na | Aortic Aneurysm, Thoracic | Withdrawn | 2019-01-01 | 2026-02-01 | ClinicalTrials.gov |
| NCT04242784 | IMPROVE Stroke Care- Developing and Optimizing Regional Systems of Stroke Care | — | Acute Stroke | Completed | 2019-01-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03730207 | Xpede Clinical Study | Na | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | Completed | 2018-12-18 | 2021-10-14 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03322033 | Feasibility of Endovascular Repair of Ascending Aortic Pathologies | Na | Dissection of Thoracic Aorta | Terminated | 2018-12-15 | 2021-10-22 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03771508 | Prospective Collection of PillCam SB3 Videos and Raw Data Files for Future Deve… | — | Small Intestine Disease | Completed | 2018-12-13 | 2025-09-30 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03763708 | SCS Research Study | Na | Limb Pain | Terminated | 2018-12-12 | 2023-01-13 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03086902 | Comparision of PVC Ablation Techniques | Na | Premature Ventricular Contraction | Unknown | 2018-12-01 | 2021-07-01 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03761316 | Goal Setting in SCS Patients: a Qualitative Review | — | Failed Back Surgery Syndrome | Completed | 2018-12-01 | 2019-03-31 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03546374 | Medtronic Terminate AF Study | Na | Persistent Atrial Fibrillation | Recruiting | 2018-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03715790 | Improve SCA Bridge Study | — | Sudden Cardiac Arrest | Completed | 2018-11-02 | 2021-05-27 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03681210 | Destination Therapy Post Approval Study | — | Chronic Heart Failure | Active_Not_Recruiting | 2018-10-31 | 2026-04-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03635424 | Medtronic Transcatheter Aortic Valve Replacement (TAVR) Low Risk Bicuspid Study | Na | Bicuspid Aortic Valve | Active_Not_Recruiting | 2018-10-30 | 2030-12-01 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT03604263 | ArcticLine Feasibility Study | Na | Atrial Fibrillation | Completed | 2018-10-18 | 2019-11-18 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT04300400 | Treatment of the Overactive Bladder Syndrome: A Delphi Study | — | Overactive Bladder Syndrome | Completed | 2018-10-16 | 2019-09-10 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03647475 | A Single Arm Trial With Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk … | Na | Coronary Artery Disease | Completed | 2018-10-01 | 2021-04-22 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03266094 | A Study of BiZact™ on Children and Adolescents Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2018-09-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03475888 | Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion R… | Na | Chronic Total Occlusion of Coronary Artery | Completed | 2018-09-28 | 2022-12-12 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03643224 | DiamondTemp™ System for the Treatment of Persistent Atrial Fibrillation | Na | Persistent Atrial Fibrillation | Completed | 2018-09-19 | 2024-10-31 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03051178 | Wearable Sensor for Responsive DBS for ET | Na | Essential Tremor | Completed | 2018-09-18 | 2021-09-29 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03577340 | Development and Validation of Performance Metrics for Cardiac Device Implant Pr… | — | Educational Problems | Unknown | 2018-09-01 | 2019-05-30 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03447938 | The Minimally Invasive Coronary Surgery Compared to STernotomy Coronary Artery … | Na | Coronary Artery Disease | Active_Not_Recruiting | 2018-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03647696 | Incidence of Opioid-Induced Respiratory Depression in Medical and Trauma Patien… | — | Respiratory Depression | Withdrawn | 2018-08-30 | 2018-08-30 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03775759 | Treatment of Tricuspid Valve Regurgitation in Patients Undergoing Left Ventricu… | Na | Tricuspid Valve Insufficiency | Completed | 2018-08-22 | 2023-02-15 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03401099 | Cryoballoon Ablation as First Line Treatment of Atrial Flutter | Na | Atrial Flutter Typical | Completed | 2018-08-17 | 2023-11-01 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03553953 | Characterization of Artifacts in the BIS™ EEG Signals in General Anesthesia Pat… | — | Anesthesia, General | Completed | 2018-08-15 | 2020-08-11 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03087084 | RESpiration deTection From Implanted Cardiac Devices in Subjects With Heart Fai… | Na | Heart Failure | Unknown | 2018-08-07 | 2020-04-01 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03585959 | superDimension™ Navigation System Version 7.2 With Fluoroscopic Navigation Tech… | Na | Lung Cancer | Completed | 2018-08-03 | 2019-02-18 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT03624504 | China Micra Transcatheter Pacing Study | Na | Bradycardia | Completed | 2018-07-31 | 2020-01-20 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT04194138 | Complex Adult Deformity Surgery (CADS) | — | Adult Spinal Deformity | Recruiting | 2018-07-30 | 2032-07-31 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03467048 | McGrath Videolaryngoscopy and Direct Laryngoscopy in Morbidly Obese Patients | Na | Morbid Obesity | Completed | 2018-07-24 | 2020-05-20 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03554486 | Evaluation of Fiasp® (Fast Acting Insulin Aspart) in 670G Hybrid Closed-Loop Th… | Phase4 | Diabetes Mellitus, Type 1 | Completed | 2018-07-23 | 2019-03-30 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608670 | Extravascular ICD Pilot Study | Na | Tachycardia | Completed | 2018-07-17 | 2023-11-15 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03504020 | ECG Belt for CRT Response | Na | Heart Failure | Completed | 2018-07-13 | 2022-04-20 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03608826 | Relationship Between LINQ™ Subcutaneous Impedance and Right-sided Hemodynamic M… | Na | Heart Failure | Completed | 2018-07-13 | 2021-05-07 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03457675 | Development of Adaptive Deep Brain Stimulation for OCD (Phase 1a) | Na | Obsessive-Compulsive Disorder | Active_Not_Recruiting | 2018-07-11 | 2027-06-01 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03437382 | Holmium Radioembolization as Adjuvant Treatment to RFA for Early Stage HCC: Dos… | Na | HCC | Completed | 2018-07-01 | 2021-03-17 | ClinicalTrials.gov |
| NCT02456922 | A Performance Evaluation of the Harmony 1 Sensors in Adults and Pediatrics | Na | Type 1 Diabetes | Withdrawn | 2018-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03417466 | A Pivotal Study to Evaluate Enlite™ Sensor Performance With iPro™2 in China | Na | Diabetes Mellitus | Completed | 2018-06-28 | 2018-09-20 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03495154 | Post Market Study of Parietene™ DS Composite Mesh in Ventral Hernia Repair | Na | Ventral Hernia | Completed | 2018-06-21 | 2022-07-06 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03586882 | Effect of Spinal Cord Stimulation on Gait and Balance in Chronic Low Back Pain … | Na | Chronic Low Back Pain | Unknown | 2018-06-15 | 2020-06-01 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT03062657 | An Investigation of the Metal Concentration in Patients Implanted With the PRES… | Na | Cervical Degenerative Disc Disease | Terminated | 2018-06-06 | 2023-01-27 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT04211441 | Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation System for… | Na | Atrial Fibrillation | Completed | 2018-06-01 | 2020-09-18 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03424941 | The TransCatheter Valve and Vessels Trial | Na | Aortic Stenosis | Completed | 2018-05-31 | 2024-06-26 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03626649 | Evaluation for the Characterization of the Safety Profile of the DiamondTemp™ S… | Na | Atrial Fibrillation | Completed | 2018-05-29 | 2019-08-08 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03362957 | Geniculate Artery Embolization for Knee Pain Secondary to Osteoarthritis (OA) | Na | Osteo Arthritis Knee | Completed | 2018-05-25 | 2020-04-24 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03584464 | RESOLUTE ONYX Post-Approval Study (Bifurcation Cohort) | Na | Coronary Artery Disease | Completed | 2018-05-14 | 2022-09-28 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03125798 | Comparison of LigaSure to Conventional Electrocoagulation in Video-assisted Tho… | Na | Lung Cancer | Completed | 2018-05-03 | 2021-11-04 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT04210622 | An Initial Assessment of the Sphere-9™ Catheter and Affera Mapping and Ablation… | — | Atrial Fibrillation | Completed | 2018-05-01 | 2020-06-18 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT06100757 | Effect of Leadless Pacing on Heart Function | Na | Pacing-Induced Cardiomyopathy | Completed | 2018-05-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT03554629 | A Comparison of Capnography Sampling Lines | Na | Capnography | Completed | 2018-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03242941 | AF Septal Pacing (Clinical Investigation Plan) | Na | Paroxysmal Atrial Fibrillation | Completed | 2018-04-26 | 2018-12-21 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT03526341 | Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fix… | — | Inguinal Hernia | Completed | 2018-04-25 | 2019-09-10 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT04495400 | Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar… | — | Lumbar Vertebral Fracture | Completed | 2018-04-23 | 2022-12-31 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03458000 | Capsule Endoscopy for HEmorrhage in the ER | Na | Upper Gastrointestinal Bleeding | Completed | 2018-04-17 | 2020-09-07 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03466151 | RESOLUTE ONYX China RCT Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-04-12 | 2026-07-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03301909 | Development of Applications of PillCam™ Endoscopy and Patency Systems and Clini… | Na | Healthy | Terminated | 2018-04-10 | 2023-03-31 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03531502 | Initial Management of Patients Receiving a Single Shock (IMPRESS) | Na | Ventricular Tachycardia | Terminated | 2018-04-09 | 2023-04-04 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03518658 | BlueSync Field Evaluation | — | Bradycardia | Completed | 2018-04-02 | 2019-12-29 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03471845 | RESOLUTE ONYX China Single Arm Study | Na | Ischemic Heart Disease | Active_Not_Recruiting | 2018-03-30 | 2026-08-30 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT03356626 | Comparison of Perioperative Outcomes Between Energy Device During Laparoscopic … | Na | Postoperative Inflammation | Completed | 2018-03-12 | 2022-08-22 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT02757976 | Resynchronization for Ambulatory Heart Failure Trial - LV Endocardial | Na | Heart Failure, Left Ventricular Dysfunction | Terminated | 2018-03-08 | 2019-06-20 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT03489187 | Visualase Visualization Database (VIVID-1) | — | Epilepsy | Completed | 2018-03-05 | 2022-04-29 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT05313984 | OptiLUTS Part C: the Development of a Symptom Assessment Tool in Sacral Neuromo… | — | Overactive Bladder Syndrome | Completed | 2018-03-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02812836 | 3D High Resolution Manometry and Balloon Expulsion Test in Diagnosis of Dyssyne… | Na | Children | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT02812823 | Comparison of Anorectal Manometry and 3D Manometry in Diagnosis of Functional D… | Na | Constipation | Unknown | 2018-03-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03335761 | InterStim® Amplitude Study | Na | Urinary Urge Incontinence | Completed | 2018-02-27 | 2019-11-06 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT03417011 | FORWARD PRO Study Interventional Post-market Study With the Evolut™ PRO System | — | Aortic Valve Stenosis | Completed | 2018-02-26 | 2024-02-26 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961465 | Effectiveness and Safety of Sacral Neuromodulation in Patients With Idiopathic … | — | Constipation | Completed | 2018-02-02 | 2021-12-31 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT03863496 | Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric … | Na | Neuromuscular Diseases | Completed | 2018-01-31 | 2021-02-14 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT04246710 | Pancreatic Cancer Molecular Sub-classification Using Endoscopic Ultrasound Tiss… | — | Pancreas Cancer | Unknown | 2018-01-28 | 2024-06-02 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03314753 | FIRE AND ICE Re-Ablations (Retrospective Data Collection) | — | Atrial Fibrillation | Completed | 2018-01-18 | 2018-06-28 | ClinicalTrials.gov |
| NCT03423459 | CoreValve Evolut Pro Prospective Registry | — | Aortic Stenosis | Unknown | 2018-01-18 | 2024-12-31 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03364023 | Post-Market Registry Of Stroke Patients Treated With Medtronic Neuro Thrombecto… | — | Stroke, Acute | Completed | 2018-01-01 | 2019-07-02 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03075748 | Visceral Manifold Study for the Repair of TAAA | Na | Thoracoabdominal Aortic Aneurysms | Active_Not_Recruiting | 2017-12-19 | 2027-02-01 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03192332 | Bridging Thrombolysis Versus Direct Mechanical Thrombectomy in Acute Ischemic S… | Na | Ischemic Stroke | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03590730 | Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyop… | — | Valvular Heart Disease | Terminated | 2017-11-15 | 2021-07-15 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT03326232 | Real-time Continuous Glucose Monitoring | Na | Gestational Diabetes | Unknown | 2017-11-13 | 2018-07-01 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT02738359 | Efficacy of Colonoscopy, Colon Capsule and Fecal Immunological Test for Colorec… | — | Colon Cancer | Completed | 2017-11-03 | 2026-01-02 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03344653 | A Randomized Controlled Trial With Resolute Onyx in One Month Dual Antiplatelet… | Na | Coronary Artery Disease | Completed | 2017-11-02 | 2020-10-09 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03496064 | Registry for Evaluating Outcome of Acute Ischemic Stroke Patients Treated With … | — | Ischemic Stroke | Completed | 2017-11-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03220659 | Optimising Pacemaker Therapy Using Multi-point Pacing (the OPT-MPP Study) | Na | Heart Failure, Systolic | Completed | 2017-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03279861 | Sacubitril-valsartan Versus Usual Anti-hypertensives in LVAD | Phase4 | Congestive Heart Failure | Withdrawn | 2017-11-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03284411 | Spinal Cord Stimulation (SCS) Dosing Study | Phase4 | Back Pain | Completed | 2017-11-01 | 2019-03-15 | ClinicalTrials.gov |
| NCT03370536 | ECGi Ibutilide: Effect of Ibutilide on AF Source Location and Organization | Na | Atrial Fibrillation | Terminated | 2017-11-01 | 2018-07-18 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03305692 | ECG Belt vs. Echocardiographic Optimization of CRT | Na | Heart Failure, Systolic | Completed | 2017-10-31 | 2021-08-17 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03245281 | LINQ for impEdance meAsuremeNt While Off From HF Medication Study | Phase4 | Heart Failure | Unknown | 2017-10-30 | 2019-04-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT02703662 | Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction | Phase2 | Ventral Hernia | Unknown | 2017-10-26 | 2025-12-01 | ClinicalTrials.gov |
| NCT03320252 | Endurant CHevAr New Indication Trial: ENCHANT | — | AAA - Abdominal Aortic Aneurysm | Active_Not_Recruiting | 2017-10-26 | 2030-07-01 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03242642 | Transcatheter Mitral Valve Replacement With the Medtronic Intrepid™ TMVR System… | Na | Mitral Valve Regurgitation | Recruiting | 2017-10-23 | 2036-09-30 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03249584 | OsteoCool Tumor Ablation Post-Market Study | Na | Metastasis Spine | Completed | 2017-10-12 | 2020-07-17 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT03260517 | The PREVAIL Study | Na | In-stent Restenosis | Completed | 2017-10-02 | 2019-08-01 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT05049486 | Computational Model of SNS (Sacral Nerve Stimulation) Induced Electrical Curren… | Na | Faecal Incontinence | Completed | 2017-10-01 | 2018-03-26 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03520127 | A Registry Study Evaluating Outcomes in Breast Biopsy With the Intact™ Breast L… | — | Breast Lesions | Terminated | 2017-09-27 | 2019-02-28 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT03210402 | REmodeling the Left Ventricle With Atrial Modulated Pacing | Na | Heart Failure | Completed | 2017-09-15 | 2021-03-15 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT02939976 | Study of Access Site for Enhancing PCI in STEMI for Seniors (SAFE STEMI for Sen… | Na | Myocardial Infarction | Terminated | 2017-08-30 | 2023-07-19 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT04024943 | Personalized Therapy Study - Attain Stability Quad Post-Approval Study | — | Heart Failure | Active_Not_Recruiting | 2017-08-21 | 2028-01-01 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03113383 | Visceral Manifold Study for the Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aortic Aneurysm | Terminated | 2017-08-18 | 2021-10-06 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03101865 | The Artificial Pancreas in Very Young Children With T1D - Pilot (KidsAP01) | Na | Type 1 Diabetes Mellitus | Completed | 2017-08-08 | 2018-05-11 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02517827 | Percutaneous Intervention Versus Surgery in the Treatment of Common Femoral Art… | Na | Peripheral Artery Disease | Unknown | 2017-08-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03111459 | Repair of Thoracoabdominal Aortic Aneurysms | Na | Thoracoabdominal Aneurysm | Recruiting | 2017-08-01 | 2029-05-01 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03434301 | Comparison of Mesh Fixation Techniques in Elective Laparoscopic Repair of Incis… | Na | Incisional Hernia | Completed | 2017-07-20 | 2020-09-22 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03088150 | COLLISION Trial - Colorectal Liver Metastases: Surgery vs Thermal Ablation | Na | ColoRectal Cancer | Unknown | 2017-07-13 | 2024-12-01 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03099655 | Attain Stability™ Quad Clinical Study | Na | Heart Failure | Completed | 2017-07-07 | 2019-05-31 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03232944 | Personalized CRT - MPP Post Approval Study | — | Heart Failure | Completed | 2017-07-05 | 2021-01-07 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT03454113 | Ellipsys Vascular Access System Registry | — | End-stage Renal Disease | Completed | 2017-07-01 | 2020-07-30 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT04208282 | Safety and Efficacy of 7-day Wear Infusion Set vs. Control Infusion Set. | Na | Type1diabetes | Completed | 2017-07-01 | 2020-03-31 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03118505 | A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation fo… | Na | Multi-Level Degenerative Lumbosacral Spinal Conditions | Active_Not_Recruiting | 2017-06-29 | 2026-12-01 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT04023461 | Isolation of Pulmonary Veins With PVAC GOLD in Elderly Patients | Phase4 | Atrial Fibrillation Paroxysmal | Completed | 2017-06-29 | 2022-06-03 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT03143257 | Ambispective Clinical Evaluation of Sophono™ | — | Conductive Hearing Loss | Completed | 2017-06-29 | 2018-05-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02913014 | Comparison of Recurrence of Atrial Fibrillation Post Cryoballon Ablation During… | Na | Atrial Fibrillation | Completed | 2017-06-28 | 2020-12-31 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT02840201 | Sub-Clinical Atrial Fibrillation Biomarker Study | — | Subclinical Atrial Fibrillation | Completed | 2017-06-26 | 2025-09-30 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03210142 | Minimally Invasive Hypoglossal Nerve Stimulation Study (Lingual Study) | Na | Sleep Apnea, Obstructive | Completed | 2017-06-23 | 2018-07-31 | ClinicalTrials.gov |
| NCT03118518 | STOP AF First: Cryoballoon Catheter Ablation in an Antiarrhythmic Drug Naive Pa… | Na | Atrial Fibrillation | Completed | 2017-06-23 | 2020-06-25 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03139721 | Medtronic HAMMOCK Post Approval Study | — | Heart Valve Diseases | Completed | 2017-06-19 | 2021-06-21 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03067480 | Comparison of 3 Versus 6-Month Use of CGMS in Non-Insulin Using T2DM Patients | Na | T2DM (Type 2 Diabetes Mellitus) | Terminated | 2017-06-06 | 2019-09-30 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT02735902 | Anticoagulation Alone Versus Anticoagulation and Aspirin Following Transcathete… | Phase4 | Transcatheter Aortic Valve Replacement | Completed | 2017-06-01 | 2024-01-19 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT03320395 | Treatment of Ex-vivo Small Bowel Mucosa With a Dedicated Radiofrequency Ablatio… | Na | Angiodysplasia | Withdrawn | 2017-06-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT04667728 | Professional Continuous Glucose Monitoring as an Adjuvant Educational Tool for … | Na | Diabetes Mellitus, Type 2 | Completed | 2017-05-30 | 2017-10-30 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT02748018 | Multi-center Trial in Adult and Pediatric Patients With Type 1 Diabetes Using H… | Na | Type 1 Diabetes | Completed | 2017-05-25 | 2023-11-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT03036345 | Cerebral Perfusion in the Beach Chair Position | Na | Cognitive Dysfunction | Unknown | 2017-05-25 | 2020-06-01 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03532347 | Endoscopic Ultrasound Guided Tissue Sampling (The SharkBITE Study) | Na | Pancreas Cancer | Completed | 2017-05-22 | 2018-11-04 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03128372 | Validation of Next Generation Cerebral and Tissue Oximeter | Na | Oxygen Deficiency | Completed | 2017-05-22 | 2017-07-19 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03148392 | Assess Differences in Pain Following Cryo and Radiofrequency Atrial Fibrillatio… | — | Atrial Fibrillation | Unknown | 2017-05-16 | 2019-12-31 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03716973 | A Study to Investigate High-density Spinal Cord Stimulation in Virgin-back Pati… | Na | Neuropathic Pain | Completed | 2017-05-09 | 2020-09-09 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03041467 | IN.PACT™ AV Access IDE Study | Na | Arteriovenous Fistula Stenosis | Completed | 2017-04-25 | 2023-05-05 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT03109132 | Comfort Check of CO2 Monitoring Cannulas With Oxygen Delivery | Na | Wearing Comfort | Completed | 2017-04-23 | 2017-08-30 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT02953418 | RFA for Flat Type High-grade and Medium-grade Intraepithelial Squamous Neoplasia | Na | Esophageal Squamous Cell Neoplasia (ESCN) | Terminated | 2017-04-20 | 2019-07-20 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03131544 | MRI Guided Transrectal Prostate Laser Ablation for Benign Prostatic Hypertrophy… | Na | BPH | Completed | 2017-04-17 | 2020-05-15 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03118531 | China Resolute Integrity 34/38 mm Study | Na | Ischemic Heart Disease | Completed | 2017-04-17 | 2023-04-28 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT03071978 | Application of Right Atrial Left Ventricular Fusion Pacing in Patients With CRT… | Na | Heart Failure | Completed | 2017-04-13 | 2019-01-29 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT02975310 | In-clinic Endoscopic Polypectomy for Chronic Sinusitis With Nasal Polyps | Na | Sinusitis | Recruiting | 2017-04-11 | 2026-12-01 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT03283722 | PRESERVE-MITRAL Post-Market Registry | — | Mitral Valve Disease | Completed | 2017-04-10 | 2021-02-10 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT02811302 | PRediction of Opioid-induced Respiratory Depression In Patients Monitored by ca… | Na | Respiratory Depression | Completed | 2017-04-07 | 2018-05-07 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03039738 | Surveillance Monitoring as an Alternative to Telemetry | Na | Telemetry | Terminated | 2017-04-03 | 2018-01-04 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03063749 | RESOLUTE ONYX Post-Approval Study | — | Coronary Artery Disease | Completed | 2017-03-30 | 2022-08-18 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03711916 | Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery | Na | Breast Cancer | Completed | 2017-03-17 | 2018-12-03 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03039712 | Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemak… | — | Bradycardia | Active_Not_Recruiting | 2017-03-10 | 2029-06-01 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT03091959 | Profiling Implantable Cardiac Device Diagnostics Trends During Clinical Events . | — | Cardiovascular Diseases | Completed | 2017-03-02 | 2018-04-30 | ClinicalTrials.gov |
| NCT03012841 | STOP Persistent AF | Na | Atrial Fibrillation | Completed | 2017-03-02 | 2019-08-13 | ClinicalTrials.gov |
| NCT02963649 | IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. P… | Na | Critical Limb Ischemia | Completed | 2017-03-02 | 2023-12-21 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT02684045 | Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFU… | — | Subjects Received MAGNIFUSE in Posterolateral Lumbar Spine | Completed | 2017-03-01 | 2017-08-15 | ClinicalTrials.gov |
| NCT03052829 | Physical Activity and Pacemaker Study | Na | Physical Activity | Completed | 2017-03-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02795962 | Direct Transfer to an Endovascular Center Compared to Transfer to the Closest S… | Na | Stroke | Completed | 2017-03-01 | 2020-10-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02793479 | Radiofrequency Ablation in Patients With Barrett's Esophagus | — | Barrett's Esophagus | Unknown | 2017-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT02961582 | Effectiveness and Cost-effectiveness of Sacral Neuromodulation in Patients With… | Na | Constipation | Completed | 2017-02-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT03050983 | Determination of the Clinical Impact of Continuous Surveillance Monitoring (SM)… | — | Respiratory Depression | Completed | 2017-02-15 | 2020-09-10 | ClinicalTrials.gov |
| NCT05063006 | Exercise Tolerance in Patients With Implanted Left Ventricular Assist Device | Na | Left Ventricular Assist Device | Completed | 2017-02-15 | 2020-08-04 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT03084458 | Does Activity Feedback Increase ICD Patient Activity Levels? | Na | ICD Patients | Completed | 2017-02-14 | 2018-06-11 | ClinicalTrials.gov |
| NCT04284033 | Evaluation of Extended Wear Infusion Set With 670G Hybrid Closed-Loop Therapy | Na | Type 1 Diabetes | Withdrawn | 2017-02-14 | 2018-04-20 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT02876575 | A Study of BiZact™ on Adults Undergoing Tonsillectomy | Na | Tonsillectomy | Completed | 2017-02-13 | 2018-10-24 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT04714385 | Medtronic PSR TDD PMCF | — | Chronic Pain | Completed | 2017-02-09 | 2024-01-18 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT02216643 | EndoVascular Treatment With Stent-retriever and/or Thromboaspiration vs. Best M… | Phase3 | Stroke | Completed | 2017-02-08 | 2019-06-30 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT02649166 | Responsive Deep Brain Stimulator for Essential Tremor | Na | Essential Tremor | Active_Not_Recruiting | 2017-02-01 | 2027-06-30 | ClinicalTrials.gov |
| NCT03044574 | Intermittent Pneumatic Compression in Surgical Patients at Extremely-high Risk … | Na | Venous Thromboembolism | Completed | 2017-02-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT02828735 | Respiration Patterns With Impedance in LINQ | Na | Breathing Exercises | Completed | 2017-01-30 | 2017-11-20 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT02825979 | Early Aggressive Invasive Intervention for Atrial Fibrillation | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT05514860 | The Impact of "First-Line" Rhythm Therapy on AF Progression | Na | Atrial Fibrillation | Unknown | 2017-01-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT03025490 | The Use of Capnography and Integrated Pulmonary Index in the Electrophysiology … | Na | Capnography | Unknown | 2017-01-01 | — | ClinicalTrials.gov |
| NCT03172520 | Automatic Periodic Stimulation and Continuous Electromyography (EMG) for Facial… | Na | Parotid Gland Disorders | Terminated | 2017-01-01 | 2017-12-30 | ClinicalTrials.gov |
| NCT06606288 | Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing… | — | Heart Failure | Active_Not_Recruiting | 2017-01-01 | 2030-12-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT03426293 | Measuring the ACT During Non-cardiac Arterial Procedures. | — | Arterial Disease | Completed | 2016-12-21 | 2024-01-31 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02733991 | Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Gluco… | Na | Type 1 Diabetes | Completed | 2016-12-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02988128 | Neurovascular Product Surveillance Registry | — | Intracranial Aneurysm | Recruiting | 2016-12-01 | 2032-08-01 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT02844465 | Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate) | Na | Temporal Lobe Epilepsy | Completed | 2016-12-01 | 2023-12-11 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT03071653 | Left Cardiac Sympathetic Denervation for Cardiomyopathy Feasibility Pilot Study | Phase2 | Dilated Cardiomyopathy | Suspended | 2016-11-24 | 2022-02-01 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02914457 | Left Ventricular Synchronous Versus Sequential MultiSpot Pacing for Cardiac Res… | Na | Heart Failure | Completed | 2016-11-07 | 2018-04-20 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02974101 | AdaptiveStim Objectifying Subjective Pain Questionnaires | Na | Failed Back Surgery Syndrome | Completed | 2016-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02506010 | Accuracy Validation of a Pulse Oximetry Monitor | — | Healthy | Withdrawn | 2016-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02979158 | Preoperative Dual Antiplatelet Therapy: Platelet Function and Influence of Card… | Na | Cardiopulmonary Bypass | Completed | 2016-11-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02548624 | An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position | — | Patient Positioning | Withdrawn | 2016-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT04350411 | Comparison of PEAK PlasmaBlade™ to Conventional Diathermy in Abdominal Based Fr… | Na | Breast Reconstruction | Completed | 2016-10-31 | 2018-05-31 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT02930980 | Micra Accelerometer Sensor Study 2 | Na | Bradyarrhythmia | Completed | 2016-10-14 | 2017-04-25 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT03071952 | Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropi… | — | Heart Failure | Completed | 2016-10-09 | 2017-11-24 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02585817 | Remote Patient Management for Cardiac Implantable Electronic Devices | Na | Arrhythmia, Cardiac | Completed | 2016-10-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02957006 | Discrimination of P and T Waves With Linq and Holter | — | Arrhythmias, Cardiac | Unknown | 2016-10-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02748434 | Glucose Variability in Subclinical Hypertrophy | Na | Diabetes Mellitus | Terminated | 2016-10-01 | 2025-09-01 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02755129 | FRailty WAlking Patterns (FRAP) Study | Na | Heart Failure | Completed | 2016-09-20 | 2017-07-20 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02901197 | Capnography At the Bedside: Leading Educational Efforts | Na | Emergency | Completed | 2016-09-15 | 2017-10-17 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02447692 | Proportional Assist Ventilation for Minimizing the Duration of Mechanical Venti… | Na | Critically Ill | Completed | 2016-09-14 | 2024-07-16 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT02915848 | Long-term Stability of LFP Recorded From the STN and the Effects of DBS | — | Parkinson's Disease | Completed | 2016-09-09 | 2021-04-26 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT04127461 | Endoscopic Harvesting in Coronary Artery Bypass Grafting. | Na | Coronary Bypass Stenosis | Completed | 2016-09-03 | 2018-12-31 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02857816 | PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial … | Na | Overactive Bladder | Completed | 2016-09-01 | 2017-11-21 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02754661 | Colon Capsule Endoscopy (CCE) Versus Computed Tomographic Colonography (CTC) in… | Na | Colorectal Cancer Screening | Completed | 2016-09-01 | 2018-08-07 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02942667 | Magnetic Resonance Imaging of Human Biometrics | — | Volunteers | Completed | 2016-08-01 | 2018-02-02 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02729077 | Risk Factors for Post-Operative Respiratory Complications in Patients at Risk f… | — | Respiratory Complications | Completed | 2016-07-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT02834689 | The Canadian E-PAraDiGM (Exercise Physical Activity and Diabetes Glucose Monito… | Na | Walking | Completed | 2016-07-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02785991 | Spanish Registry of Cryoballoon Ablation | — | Atrial Fibrillation | Completed | 2016-07-01 | 2021-04-14 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02742714 | PillCam SBC System Functionality in Established and Suspected IBD Patients | Na | Chronic Inflammatory Small Bowel Disease | Completed | 2016-07-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02943941 | Pressure Variability Study | Na | Heart Failure | Completed | 2016-07-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02673021 | MARK 1A Series: Percutaneous Microwave Ablation for Patients With Lung Tumor(s) | Na | Lung Neoplasms | Terminated | 2016-06-08 | 2020-03-13 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02758301 | Reveal LINQ™ Heart Failure | — | Heart Failure | Completed | 2016-06-08 | 2018-12-04 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02746809 | Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum) | Na | Aortic Valve Stenosis | Completed | 2016-06-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02651181 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Completed | 2016-06-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02787265 | High-density in Spinal Cord Stimulation: Virtual Expert Registry | — | Failed Back Surgery Syndrome | Completed | 2016-06-01 | 2020-12-08 | ClinicalTrials.gov |
| NCT02850107 | DiRectional AthErectomy + Drug CoAted BaLloon to Treat Long, CalcifIed Femoropo… | Na | Peripheral Vascular Disease | Completed | 2016-06-01 | 2020-06-16 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02678442 | Endoscopic Ultrasound Guided Fine Needle Biopsy (EUS-FNB-SC) Using a Novel Fork… | Na | Pancreatic Cancer | Completed | 2016-05-16 | 2018-11-10 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02594488 | Implantable Cardiac Monitors in High-Risk Post-Infarction Patients With Cardiac… | Na | Myocardial Infarction | Completed | 2016-05-06 | 2021-02-01 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02752737 | Cryo Global Registry | — | Atrial Fibrillation | Completed | 2016-05-02 | 2024-11-29 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02673502 | Pre-operative Carbohydrate Drink to Preserve Peri-operative Insulin Sensitivity | Na | Laparoscopic Abdominal Surgery | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02772380 | Acute Study to Collect Electrical Signals From the Heart Using a Special Lead | Na | Tachycardia | Completed | 2016-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02698241 | Integrated Diagnostics Driven Diuretic and Chronic Medication Management for He… | Na | Heart Failure | Terminated | 2016-05-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02707289 | Retrospective Collection of PillCam SB Movies | — | Inflammatory Bowel Disease, Crohn Disease | Completed | 2016-05-01 | 2018-06-18 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02903823 | Intrathecal (IT) Baclofen Drug Distribution | Phase4 | Muscle Spasticity | Completed | 2016-04-22 | 2019-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02660827 | Safety Evaluation of the Hybrid Closed Loop (HCL) System in Pediatric Subjects … | Na | Type 1 Diabetes | Completed | 2016-04-18 | 2021-02-01 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02738853 | The Medtronic TAVR 2.0 US Clinical Study | Na | Aortic Valve Stenosis | Completed | 2016-04-01 | 2021-12-15 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02809131 | Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Devi… | Phase3 | Sick Sinus Syndrome | Completed | 2016-04-01 | 2021-09-30 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02969395 | 3T MRI CIED Post-Approval Study | — | Cardiac Rhythm Disorder | Completed | 2016-04-01 | 2021-10-15 | ClinicalTrials.gov |
| NCT02652949 | Valiant Evo US Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02749201 | Transmitted Light Tissue Thickness Analysis (TiLTT) | Na | Morbid Obesity | Completed | 2016-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02625324 | Valiant Evo International Clinical Trial | Na | Aortic Aneurysm, Thoracic | Completed | 2016-04-01 | 2023-03-02 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02659280 | Using "Store and Forward" Tele-health as an Adjunct to Traditional Outpatient o… | Na | Chronic Disease | Completed | 2016-03-16 | 2017-11-10 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02712515 | The Motor Network in Essential Tremor: Mechanisms of Therapy | — | Essential Tremor | Completed | 2016-03-15 | 2025-10-13 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02719522 | Pipeline Flex With SHield Technology Embolization - An International MulticEnte… | — | Intracranial Aneurysm | Completed | 2016-03-01 | 2019-08-22 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02681731 | Impact of Neuromonitoring During Cardiac Procedures | — | Delirium | Completed | 2016-03-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02686814 | PERIGON Japan Trial | Na | Aortic Stenosis | Completed | 2016-03-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT02687256 | Evaluation of Extended Infusion Set Wear Using Medtronic Extended Wear Sof-set … | Phase1 | Type 1 Diabetes | Completed | 2016-03-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT02701283 | Medtronic Evolut Transcatheter Aortic Valve Replacement in Low Risk Patients | Na | Aortic Valve Stenosis | Active_Not_Recruiting | 2016-03-01 | 2029-06-01 | ClinicalTrials.gov |
| NCT02718131 | A Study of INFUSE Bone Graft (BMP-2) in the Treatment of Tibial Pseudarthrosis … | Na | NF1 | Terminated | 2016-03-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT03223207 | CareLink Express (CLE Research) | — | Atrial Fibrillation | Completed | 2016-03-01 | 2018-08-27 | ClinicalTrials.gov |
| NCT02775708 | Development of Applications of the ® PillCam Endoscopy System and Evaluation of… | Na | Any Gastric Condition Which Requires Capsule Endoscopy | Completed | 2016-03-01 | 2017-10-24 | ClinicalTrials.gov |
| NCT02700945 | Rate of Atrial Fibrillation Through 12 Months in Patients With Recent Ischemic … | Na | Stroke, Acute | Completed | 2016-03-01 | 2022-07-28 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT03175419 | BReLLS: A Prospective Belgian Registry on Laparoscopic Liver Surgery | — | Laparoscopic Liver Surgery | Completed | 2016-02-16 | 2022-12-31 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02263222 | A Feasibility Dose-escalating Study of MDT-10013 for Acute Postoperative Pain F… | Phase2 | Post-operation Pain | Withdrawn | 2016-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02759237 | The Medtronic Transcatheter Aortic Valve Implant System (CoreValve System Famil… | — | Symptomatic Aortic Stenosis | Terminated | 2016-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02692547 | Feasibility Study to Evaluate the Hybrid-Logic Closed Loop System in Type 1 Dia… | Na | Type 1 Diabetes | Withdrawn | 2016-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02707003 | Clinical Utility of Capnography in the PACU( Post-anaesthesia Care Unit) | — | Respiratory Depression | Completed | 2016-02-01 | 2018-06-15 | ClinicalTrials.gov |
| NCT02497014 | The European Bifurcation Club Left Main Study | Na | Percutaneous Transluminal Coronary Angioplasty | Unknown | 2016-02-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT02727192 | Effect of Treatment of Sleep Apnea in Patients With Paroxysmal Atrial Fibrillat… | Na | Sleep Disordered Breathing | Completed | 2016-01-21 | 2020-09-01 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT03404128 | Long Term Follow-up of Hippocampal DBS for Refractory Epilepsy | — | Refractory Epilepsy | Completed | 2016-01-11 | 2021-04-20 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02662842 | BD FlowSmart™ Subcutaneous Insulin Infusion Set User Preference and Claims Study | — | Type 1 Diabetes Mellitus | Completed | 2016-01-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT03112538 | Improving Glycaemic Control in Malaysian Patients With Type 2 Diabetes Mellitus… | Phase4 | Type 2 Diabetes Mellitus | Unknown | 2016-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02650349 | StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimula… | Na | Failed Back Surgery Syndrome | Completed | 2016-01-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT01877486 | PVI Using Cryoablation Alone in Paroxysmal AF Patients Converted From Persisten… | — | Paroxysmal Atrial Fibrillation | Withdrawn | 2016-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02821351 | ACT DiamondTemp TempeRAture-Controlled and Contact Sensing RF Ablation Clinical… | Na | Paroxysmal Atrial Fibrillation | Completed | 2016-01-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02671903 | The His Optimised Pacing Evaluated for Heart Failure Trial (HOPE-HF). | Na | Heart Failure | Completed | 2016-01-01 | 2020-10-31 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02592369 | CoreValve™ Evolut R™ FORWARD Study | — | Aortic Valve Stenosis | Completed | 2016-01-01 | 2020-02-06 | ClinicalTrials.gov |
| NCT02646878 | A Feasibility Study to Evaluate the Performance of the Harmony 1 Sensors in Adu… | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02649010 | A Performance Evaluation of the Enlite 3 Sensor | Na | Type 1 Diabetes | Withdrawn | 2016-01-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02541617 | Hub and Spoke, Comparative Outcomes for Parkinson's Disease Treated With Deep B… | Na | Parkinson's Disease | Withdrawn | 2016-01-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02494284 | Short-Term Dual Antiplatelet and Maintenance CloPidogrel Therapy After Drug-Elu… | Phase4 | Coronary Artery Disease | Terminated | 2015-12-22 | 2017-02-13 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT02424370 | Geriatric Evaluation to Predict Mortality and Functional Recovery After Trans A… | — | Symptomatic Aortic Stenosis | Completed | 2015-12-09 | 2020-01-23 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT02427126 | Apixaban for Treatment of Embolic Stroke of Undetermined Source | Phase3 | Embolic Stroke of Undetermined Source | Completed | 2015-12-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT01985802 | Pacing in First-degree AV-block | Na | First-degree AV-block | Completed | 2015-12-01 | 2017-10-26 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02570906 | Performance Assessment of a Remote Patient Monitoring Device | — | Physiologic Monitoring | Completed | 2015-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT02617563 | 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Dege… | — | Intervertebral Disc Degeneration | Completed | 2015-12-01 | 2024-11-14 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT03960346 | Cryoballoon and Associated Esophageal Effects | Na | Atrial Fibrillation | Completed | 2015-11-25 | 2018-05-02 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02608177 | Continuous Glucose Monitoring to Assess Glycemia in Chronic Kidney Disease - Ch… | Na | Chronic Kidney Diseases | Completed | 2015-11-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02564419 | Brain Machine Interface (BMI) in Subjects Living With Quadriplegia | Na | Spinal Cord Injury | Completed | 2015-11-01 | 2019-11-30 | ClinicalTrials.gov |
| NCT02699944 | Optimization of CRT Using an ECG Vest | Na | Heart Failure | Completed | 2015-11-01 | 2021-08-17 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02657421 | OLIF25™ /OLIF51™ Study | — | Degenerative Disc Disease | Terminated | 2015-11-01 | 2018-05-03 | ClinicalTrials.gov |
| NCT02683135 | Lifestyle Control of Postprandial Hyperglycemia | Na | Type 2 Diabetes | Completed | 2015-11-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02393573 | Attenuating The Post-Operative Insulin Resistance And Promoting Protein Anaboli… | Na | Pre-Diabetes | Terminated | 2015-11-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02415556 | Memory Aid by Intranasal Insulin in Diabetes (MemAID) | Phase2 | Type 2 Diabetes Mellitus | Completed | 2015-10-06 | 2020-05-31 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02588144 | Combined Stimulation of STN and SNr for Resistant Freezing of Gait in Parkinson… | Na | Parkinson's Disease | Unknown | 2015-10-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02621528 | Lifetech CeraFlex™ Post-Market Surveillance Study | Na | Patent Foramen Ovale | Completed | 2015-10-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02593994 | IRIS-Onyx Cohort in the IRIS-DES Registry | — | Coronary Artery Disease | Active_Not_Recruiting | 2015-10-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02551302 | "Efficacy of Hybrid Systems ("Topping Off") Versus Rigid Spinal Fusion in Lumba… | Na | Spine Surgery | Unknown | 2015-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02357121 | Focal Laser Ablation of Prostate Tissue | Early_Phase1 | Prostate Cancer | Completed | 2015-09-17 | 2019-08-20 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02604303 | A Prospective Analysis on the Expansion Rates of Abdominal Aortic Aneurysms | — | Abdominal Aortic Aneurysm | Unknown | 2015-09-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02849769 | Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-appro… | — | Tachyarrhythmia | Completed | 2015-09-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02438033 | Characterizing the Specificity and Stability of Local Field Potentials in the G… | Phase1 | Parkinson's Disease | Withdrawn | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02058940 | Intravenous Exenatide in Patients With Acute Brain Injury | Phase4 | Brain Injuries | Completed | 2015-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02672969 | The Evaluation of Pre-Post Smoke Evacuation Uses on Surgical Smoke and Bio-Aero… | Na | Smoke | Unknown | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02773420 | HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment | Na | Hemorrhoids | Completed | 2015-08-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02491554 | Deep braIn Stimulation for Tremor TractographIC Versus Traditional | Na | Essential Tremor | Unknown | 2015-08-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02439775 | SPYRAL HTN-ON MED Study of Renal Denervation With the Symplicity Spyral™ Multi-… | Na | Hypertension | Completed | 2015-07-22 | 2025-08-14 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02419521 | Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study | Na | Coronary Artery Disease | Completed | 2015-07-07 | 2018-12-03 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02503787 | OPTIONS Spinal Cord Stimulation Programming Parameters | Na | Pain, Intractable | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02536118 | Micra Transcatheter Pacing System Post-Approval Registry | — | Bradycardia | Active_Not_Recruiting | 2015-07-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02468843 | Novel Stimulation Patterns for the Treatment of Dystonia | — | Dystonia | Completed | 2015-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02509325 | Parkinson's KinetiGraph as Tool for DBS Eligibility Assessment | — | Parkinson's Disease | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02428140 | Post-Embolic Rhythm Detection With Implantable Versus External Monitoring | Na | Stroke | Completed | 2015-07-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02417259 | Near Infrared Spectroscopy in Cyanotic Congenital Heart Disease | — | Congenital Heart Defects | Completed | 2015-07-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT04543747 | Mechanical Circulatory Support Korea Post Market Surveillance Study (PMS) | — | End-stage Heart Failure | Completed | 2015-06-11 | 2020-12-05 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02463097 | Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2015-06-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT01014000 | Comparative Study to Examine Whether Echocardiography Performed During Cardiac … | Na | Heart Failure | Withdrawn | 2015-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT02493205 | The Holding Area LINQ (Reveal LINQ Insertable Cardiac Monitor) Trial is a Prosp… | — | Coronary Artery Disease | Completed | 2015-06-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT03786822 | Reduction of Radiation Dose and Contrast Use During Cryoballoon Pulmonary Vein … | Na | Atrial Fibrillation | Completed | 2015-06-01 | 2016-12-20 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01880164 | Cost Effectiveness of Nonoperative Management for Adult Spinal Deformity | — | Spinal Deformity | Completed | 2015-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02371122 | Spinal Cord Stimulation (SCS) Therapy Study | Na | Failed Back Surgery Syndrome | Withdrawn | 2015-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02484898 | SEEQ™ Performance Study | — | Arrhythmia Type Unknown | Completed | 2015-06-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02444156 | Rowing Away From Diabetes | Na | Diabetes Mellitus, Type 2 | Completed | 2015-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02461524 | Endurant Evo International Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-06-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02439749 | SPYRAL PIVOTAL - SPYRAL HTN-OFF MED Study | Na | Hypertension | Completed | 2015-06-01 | 2023-10-25 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02488681 | Micra Transcatheter Pacing System Continued Access Study Protocol | Na | Bradycardia | Completed | 2015-06-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02378883 | Apollo™ Onyx™ Delivery Microcatheter Post Market Safety Study | Na | Arteriovenous Malformations | Completed | 2015-05-18 | 2018-02-20 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01938248 | Apixaban for the Reduction of Thrombo-Embolism in Patients With Device-Detected… | Phase4 | Atrial Fibrillation | Completed | 2015-05-01 | 2023-11-03 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02500537 | A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technol… | Na | Non-emergent, Abdominal or Thoracic Procedures | Completed | 2015-05-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT03151018 | Effect and Efficacy of Onyx™, Zotarolimus-eluting Stent for Coronary Atheroscle… | — | Coronary Artery Disease | Unknown | 2015-05-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02467140 | Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Me… | Na | Inguinal Hernia | Unknown | 2015-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02365467 | Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TA… | — | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | Completed | 2015-04-16 | 2024-12-05 | ClinicalTrials.gov |
| NCT02410837 | NAVIGATE: Clinical Evaluation of superDimension™ Navigation System for Electrom… | — | Lung Lesion(s) Requiring Evaluation | Completed | 2015-04-16 | 2019-11-01 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02412501 | Medtronic Resolute Onyx 2.0 mm Clinical Study | Na | Coronary Artery Disease | Completed | 2015-04-06 | 2019-02-21 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02430571 | Case Series to Evaluate the Identification of Anatomical Markers Using the KANG… | — | Enteral Nutrition, Feeding Tube Placement | Completed | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02393716 | Endurant Evo US Clinical Trial | Na | Abdominal Aortic Aneurysm | Terminated | 2015-04-01 | 2021-06-25 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02322840 | Transcatheter Mitral Valve Replacement System (TMVR) Pilot Study and The Early … | Na | Mitral Valve Insufficiency | Active_Not_Recruiting | 2015-04-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02423798 | New Generation Enlite Accuracy Study | Na | Diabetes | Completed | 2015-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02655666 | Qingdao: Insulin Pump Follow-Up Program | — | Type 1 Diabetes | Terminated | 2015-04-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT02395536 | Medtronic Reveal LINQ™ In-Office 2 (RIO 2) Study United States | Na | Arrhythmia | Completed | 2015-03-30 | 2016-05-31 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT04141111 | Retrospective and Prospective Study on Professional Continuous Glucose Monitori… | Na | Diabetes Mellitus, Type 2 | Completed | 2015-03-22 | 2018-03-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02433613 | Postmarket Evaluation of the Phased Radio Frequency Ablation System (GOLD AF Re… | — | Atrial Fibrillation | Completed | 2015-03-01 | 2019-05-01 | ClinicalTrials.gov |
| NCT02390037 | Pipeline™ Flex Embolization Device With Shield Technology™ Clinical Study | — | Aneurysm | Completed | 2015-03-01 | 2016-11-04 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02363894 | DEFINITIVE AR Two Year Follow-up Extension Study | — | Peripheral Arterial Disease | Completed | 2015-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02325193 | "MiniMed 640G System" User Evaluation With the Question of Reducing the Rate of… | — | Type 1 Diabetes | Completed | 2015-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02363972 | Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD | Na | End Stage Renal Disease | Completed | 2015-02-10 | 2016-06-01 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02624414 | Capsule Colonoscopy in Crohn's Disease and Its Correlation With Conventional Co… | Na | Crohn's Disease | Completed | 2015-02-06 | 2022-05-05 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02227121 | Acute Defibrillation Study | Na | Ventricular Arrhythmias | Terminated | 2015-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02343016 | NIRS as a Continuous Noninvasive Monitoring System of Liver/Kidney Graft Perfus… | — | Liver Failure | Terminated | 2015-02-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02530203 | Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation | Na | Atrial Fibrillation | Terminated | 2015-02-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02412488 | Reveal LINQ™ In-Office 2 (RIO2) Study International | Na | Arrhythmia | Completed | 2015-02-01 | 2016-10-20 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02306304 | Ultra-sound for AAA Screening in Smoking Israeli Arab Men | Na | Abdominal Aortic Aneurysm (AAA) | Completed | 2015-01-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02314598 | Therapy Coil Electrogram Collection Study | — | Lead Insulation Failure | Terminated | 2015-01-01 | 2017-09-14 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02318927 | A Responsive Closed-Loop Approach to Treat Freezing of Gait in Parkinson's Dise… | Na | Parkinsons Disease | Completed | 2015-01-01 | 2018-09-26 | ClinicalTrials.gov |
| NCT02323854 | The EMPrint™ Ablate and RESect Study in Patients With Metastatic Lung Tumors (E… | Na | Lung Cancer | Completed | 2015-01-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02275208 | A Prospective, Multi-center, Single-arm Study of the Stomach, Intestinal and Py… | — | Obesity | Completed | 2014-12-11 | 2017-01-18 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02213731 | Cryoballoon Ablation for Early Persistent Atrial Fibrillation (Cryo4 Persistent… | Na | Atrial Fibrillation | Completed | 2014-12-08 | 2017-09-12 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02284347 | NuVent™ Revision Study | Na | Chronic Rhinosinusitis | Completed | 2014-12-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02705950 | Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. | Na | Neuropathic Pain | Completed | 2014-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02301429 | Model 20105 Lead Study | Na | Sick Sinus Node Syndrome | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02326493 | Tailor-CRT: Better Application of Cardiac Resynchronization Therapy | Na | Heart Failure | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02268942 | HW006 LATERAL Thoracotomy | Na | Left Sided Heart Failure | Completed | 2014-11-01 | 2018-10-01 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02209298 | CoreValve VIVA Study Evaluation of the Clinical Outcomes of CoreValve in Degene… | — | Aortic Valve Stenosis | Completed | 2014-11-01 | 2018-12-03 | ClinicalTrials.gov |
| NCT02247765 | Controlled Acute Hypoxia Study Comparing Pulse Oximetry to Arterial Blood Sampl… | Phase3 | Healthy | Completed | 2014-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02347189 | Melody PB1016 Surveillance Study | Na | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | Completed | 2014-11-01 | 2018-08-10 | ClinicalTrials.gov |
| NCT02140567 | Syncope Prediction Study | — | Vasovagal Syncope | Completed | 2014-11-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02106910 | Non-Endoscopic Surveillance for Barrett's Esophagus Following Ablative Therapy | Na | Barrett's Esophagus | Completed | 2014-10-27 | 2018-08-14 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02222818 | Cardiac Resynchronization Therapy Efficacy Enhancements | Na | Atrial Fibrillation | Completed | 2014-10-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02130284 | In Clinic Evaluation of the PLGM Feature | Na | Type 1 Diabetes | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02280187 | InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, … | — | Spine Fusion | Completed | 2014-10-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02217254 | The OneFreeze Study | Na | Paroxysmal Atrial Fibrillation | Completed | 2014-10-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02428010 | Twelve Transcatheter Mitral Valve Replacement (TMVR) Pilot Study | Na | Mitral Valve Insufficiency | Terminated | 2014-09-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02246582 | Adult Accuracy Study of the Enlite 3 Glucose Sensor | Na | Type 1 Diabetes | Completed | 2014-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02241382 | Cologne Cardioversion Study | Na | Atrial Arrhythmia | Completed | 2014-09-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT02265783 | Sensor Off Study Using a Nellcor USB Pulse Oximetry Monitor Interface Cable | Na | Healthy Volunteers | Completed | 2014-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02365688 | Hemodynamic Response During Goal Directed Fluid Therapy in the OR | Na | Hemodynamic Instability | Terminated | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02934789 | Effectiveness of Truclear on Patient Quality of Life | Na | Heavy Menstrual Bleeding | Completed | 2014-09-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT03039374 | External Phase MRI in Diagnosis of OASI | — | Anal Sphincter Injury | Completed | 2014-09-01 | 2017-10-27 | ClinicalTrials.gov |
| NCT02328040 | Randomized Trial Comparing Sitagliptin to Placebo in Closed Loop | Phase1 | Diabetes Mellitus, Type 1 | Completed | 2014-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02100722 | A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Interventi… | Na | Coronary Disease | Completed | 2014-08-25 | 2024-12-01 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02239640 | Systematic Evaluation of Patients Treated With Stroke Devices for Acute Ischemi… | — | Ischemic Stroke | Completed | 2014-08-21 | 2016-10-07 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02294331 | Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance St… | — | Heart Failure | Completed | 2014-08-01 | 2021-07-31 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02216344 | Controlled Acute Hypoxia Study - Abbreviated Sensor Line | — | Healthy | Completed | 2014-08-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02186041 | Sacral Neuromodulation With InterStim® Therapy for Intractable Urinary Voiding … | — | Urinary Incontinence | Completed | 2014-08-01 | 2021-03-22 | ClinicalTrials.gov |
| NCT02631525 | Recovery Profile Comparison Between Remifentanil-propofol or Desflurane Anesthe… | Phase4 | Delayed Emergence From Anesthesia | Completed | 2014-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02207569 | Medtronic CoreValve Evolut R U.S. Clinical Study | Na | Aortic Stenosis | Completed | 2014-08-01 | 2020-10-28 | ClinicalTrials.gov |
| NCT02250521 | McGRATH MAC Video Laryngoscope | Na | Intubation; Difficult | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02205359 | AdaptResponse Clinical Trial | Na | Heart Failure With Left Bundle Branch Block | Completed | 2014-08-01 | 2022-11-02 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02199080 | D-dimer Assay for the Exclusion of Intra-atrial Thrombus Risk Before Ablation o… | Na | Atrial Fibrillation | Completed | 2014-07-28 | 2016-05-01 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT02186561 | Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embo… | Na | Intracranial Aneurysm | Completed | 2014-07-24 | 2018-12-13 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT01844037 | OneShot Renal Denervation Registry | Phase2 | Hypertension | Terminated | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02212470 | Drug Eluting Balloon Angioplasty Versus Nitinol Stent Implantation in the Super… | Phase4 | Peripheral Arterial Disease | Completed | 2014-07-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02189161 | A Safety and Tolerability of Circumferential Anal Canal Radiofrequency Ablation… | Na | Anal Intraepithelial Neoplasia (AIN) | Completed | 2014-07-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02238743 | Assuring and Defining Outcomes Through Procedural Training Using a Proctorship … | — | Hernia | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02535884 | Deep Brain Stimulation (DBS) of the Globus Pallidus (GP) in Huntington's Diseas… | Na | Huntington Disease | Completed | 2014-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02180958 | Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs | — | Cerebral Arteriovenous Malformations | Completed | 2014-07-01 | 2021-10-01 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02206828 | The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Vent… | — | Ventral Incisional Hernia | Completed | 2014-06-25 | 2017-05-22 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02381574 | French Lumbar Total Disk Replacement Observational Study | — | Lumbar Total Disk Replacement | Unknown | 2014-06-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02165709 | Cohort Study of Risk Reducing Salpingectomy | Na | Sterilization, Tubal | Completed | 2014-06-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02120794 | Threshold Suspend in Pediatrics at Home | Na | Type 1 Diabetes | Completed | 2014-06-01 | 2017-06-16 | ClinicalTrials.gov |
| NCT01889485 | Screening and Access to Health Care for Vascular Disease | — | Aortic Aneurysm, Abdominal | Completed | 2014-06-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02358603 | Chronotropic Incompetence (CI) Diagnostic Algorithm in Heart Failure Patients | Na | Heart Failure | Terminated | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02169921 | TurboHawk™ Japan Trial in Patients With PAD | Na | Peripheral Arterial Disease | Completed | 2014-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01803438 | Catheter Cryoablation Versus Antiarrhythmic Drug as First-Line Therapy of Parox… | Phase4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | Completed | 2014-06-01 | 2020-01-20 | ClinicalTrials.gov |
| NCT02366767 | Assessment of an Automatic Closed-loop Insulin Delivery System | Na | Diabetes Mellitus, Type 1 | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02488837 | Investigation of Non-Invasive Outcomes Predictors in Patients Undergoing DBS fo… | — | Movement Disorders | Completed | 2014-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02088554 | PERIGON Pivotal Trial | Na | Aortic Stenosis | Active_Not_Recruiting | 2014-05-12 | 2035-12-31 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02149654 | Engager Align Post-market Clinical Study | — | Aortic Valve Stenosis | Completed | 2014-05-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02401659 | Importance of Patient´s Satisfaction With Telemedicine Based on Monitoring Syst… | — | Arrythmia | Completed | 2014-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02098876 | Wall Shear Stress and Neointimal Healing Following PCI in Angulated Coronary Ve… | Na | Coronary Artery Disease | Completed | 2014-05-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02145546 | Antiarrhythmic Drugs Assessment in Preventing Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2014-05-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02155517 | Clinical Effect of Two Pharmacokinetics Model of Propofol | Phase4 | Healthy | Completed | 2014-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02115802 | LFP Correlates of Movement Disorders | Na | Parkinson's Disease | Unknown | 2014-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02025777 | Evaluation of PillCam IBD Capsule Endoscopy System in Visualization of Lesions … | Na | Ulcerative Colitis | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02086019 | Revascularisation or Medical Therapy in Elderly Patients With Acute Anginal Syn… | Na | Acute Coronary Syndromes | Completed | 2014-05-01 | 2019-12-12 | ClinicalTrials.gov |
| NCT02147769 | Cerebral Oxygenation and Autoregulation in Preterm Infants | — | Intraventricular Hemorrhage of Prematurity | Completed | 2014-05-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02504632 | Study of Platelet Activation by Severe Aortic Stenosis and Its Correction by Tr… | Na | Aortic Stenosis | Completed | 2014-05-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02145351 | Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Fa… | Na | Heart Failure With a Preserved Ejection Fraction | Completed | 2014-04-07 | 2022-05-09 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT01995552 | IdeNtifying High riSk Patients Post Myocardial Infarction With REduced Left Ven… | Na | Post MI Left Ventricular Dysfunction | Completed | 2014-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02134379 | Dynamic Thoracic Impedance as a Marker for Heart Failure Decompensation | — | Heart Failure; With Decompensation | Completed | 2014-04-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT01970501 | Genetically Targeted Therapy for the Prevention of Symptomatic Atrial Fibrillat… | Phase2 | Current or Recent History of Atrial Fibrillation | Completed | 2014-04-01 | 2017-12-28 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT02124018 | Risk Stratification in Patients With Preserved Ejection Fraction | — | Myocardial Infarction | Completed | 2014-04-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01825239 | Virtual LV Lead Navigation in Patients With Ischemic Cardiomyopathy | Na | Cardiomyopathy | Withdrawn | 2014-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02746471 | Reveal LINQ Registry | — | Arrhythmias, Cardiac | Completed | 2014-04-01 | 2021-06-04 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02056873 | Tourette Syndrome Deep Brain Stimulation | Na | Tourette Syndrome | Completed | 2014-03-20 | 2023-08-24 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02081742 | Comparative Study of Colon Capsule and Virtual Colonoscopy (VICOCA) | — | Colonic Polyps | Completed | 2014-03-12 | 2016-06-01 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02099721 | Improve Sudden Cardiac Arrest Study | Na | Sudden Cardiac Arrest | Completed | 2014-03-01 | 2018-09-05 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02118532 | The IN.PACT SFA Clinical Study for the Treatment of Atherosclerotic Lesions in … | Na | Atherosclerosis | Completed | 2014-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02091440 | Clinical Evaluation of HW005 Ventricular Assist System for the Treatment of Adv… | Na | Heart Failure | Completed | 2014-03-01 | 2018-12-06 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02066740 | EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinica… | Na | Peripheral Arterial Diseases | Completed | 2014-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02052453 | ICD-ON Registry: Periop Management of Cardiac Devices | — | Oversensing Cardiac Pacemaker | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01945138 | Closed Loop Insulin Pump Therapy After Islet Auto-Transplantation | Na | Chronic Pancreatitis | Completed | 2014-02-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02036333 | The Role of Cerebral Oximetry in Pediatric Concussion Assessment | — | Concussion, Brain | Terminated | 2014-01-01 | 2015-06-30 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02491853 | The Gulf Implantable Cardioverter-Defibrillator Registry | — | Implantable Defibrillator User | Completed | 2014-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02040571 | The Performance of an Artificial Pancreas at Home in People With Type 1 Diabetes | Na | Type 1 Diabetes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02071511 | Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation … | Na | Ventricular Tachycardia | Terminated | 2014-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02816398 | Catheter System Feasibility Clinical Trial | Na | Renal Insufficiency, Chronic | Completed | 2014-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02022826 | Clinical Management With SPM System and Validation of the SPM 5 Hour Cutoff in … | Na | Gastroparesis | Terminated | 2014-01-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT02046330 | Deep Brain Stimulation (DBS) Therapy for Treatment Resistant Depression | Na | Major Depressive Disorder | Active_Not_Recruiting | 2013-12-16 | 2027-04-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02125097 | The Reverse Barrel™ VRD Intracranial Aneurysm Trial | Na | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-12-12 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02294370 | Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Mo… | — | Diabetes Mellitus, Type 2 | Completed | 2013-12-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01954160 | Study of Renal Denervation in Patients With Heart Failure | Phase2 | Heart Failure | Terminated | 2013-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT02003898 | Post Approval Study of the TS Feature With the 530G Pump System Supplemented Wi… | Na | Diabetes | Completed | 2013-11-26 | 2018-02-20 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02075346 | Bedside Respiratory Patient Monitoring System - Sensor Off Study | — | Healthy Volunteers | Completed | 2013-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01991548 | User Evaluation of the MiniMed 640G Insulin Pump | Na | Type 1 Diabetes | Completed | 2013-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02541773 | Novel Vascular Biomarkers Behaviour and Clinical Value in Heart Failure and CRT | — | Chronic Heart Failure | Unknown | 2013-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT01934296 | Chronic Effects of DBS in Parkinson's Disease and Dystonia | Na | Parkinson's Disease | Completed | 2013-11-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT01693120 | Evaluation of the Phased Radio Frequency Ablation System | Na | Persistent Atrial Fibrillation | Terminated | 2013-11-01 | 2017-02-07 | ClinicalTrials.gov |
| NCT02004873 | Micra Transcatheter Pacing Study | Na | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | Completed | 2013-11-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01924182 | Intrathecal Morphine Compared to Conventional Medical Management for Pain Contr… | Na | Chronic Pain | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01966458 | A Clinical Trial to Evaluate the HeartWare™ Ventricular Assist System (ENDURANC… | Na | Chronic Heart Failure | Completed | 2013-10-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01990313 | Neural Signatures of Parkinson's Disease | Na | Parkinson's Disease | Completed | 2013-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01876420 | The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study | Na | Aortic Stenosis | Completed | 2013-10-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01895140 | A Study of Renal Denervation in Patients With Treatment Resistant Hypertension | Na | Treatment-Resistant Hypertension | Terminated | 2013-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02178228 | Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected | — | Anastomotic Leaks | Completed | 2013-10-01 | 2018-01-31 | ClinicalTrials.gov |
| NCT01972139 | Renal Denervation in Patients With Uncontrolled Hypertension - SYMPLICITY HTN-4 | Na | Hypertension | Completed | 2013-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01632943 | Single-arm Study of Symplicity™ Renal Denervation System in Patients With Uncon… | Na | Adults With Uncontrolled Hypertension | Terminated | 2013-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01972126 | MAGNetic QRS-Fragmentation in Patients With Myocardial InfarcTion and Moderatel… | — | Acute Myocardial Infarction | Terminated | 2013-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01956578 | REVEAL for Respiration Detection | Na | Unexplained Syncope | Unknown | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT01965899 | Usability Study to Assess the Reveal LINQ Insertable Cardiac Monitor System | Na | Syncope | Completed | 2013-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01950715 | Multimodal Stimulation Before and After Sacral Nerve Stimulation for Irritable … | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01948973 | Subsensory Sacral Nerve Stimulation for Irritable Bowel Syndrome | Na | Irritable Bowel Syndrome | Completed | 2013-09-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02294929 | Cryoballoon Ablation in Patients With Longstanding Persistent Atrial Fibrillati… | Na | Atrial Fibrillation | Unknown | 2013-09-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01939392 | Rapid Renal Sympathetic Denervation for Resistant Hypertension II | Phase2 | Resistant Hypertension | Withdrawn | 2013-09-01 | 2018-09-01 | ClinicalTrials.gov |
| NCT02026635 | Cardiac Compass With Optivol® to Negate Future Inpatient Re-admissions Through … | — | Heart Failure | Withdrawn | 2013-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01957137 | InterStim® Sacral Nerve Modulation Cycling Study | Na | Urinary Urge Incontinence | Completed | 2013-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01798797 | Integrated Diagnostic for Heart Failure | — | Heart Failure | Completed | 2013-08-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01788085 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Na | Gastro Esophageal Reflux Disease | Withdrawn | 2013-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01944228 | Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a Pilot Study | Phase1 | Inflammation | Completed | 2013-08-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01942720 | Monitoring Disease Activity Using Video Capsule Endoscopy (VCE) in Crohn's Dise… | Na | Known Crohn Disease Subjects | Completed | 2013-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01981590 | Mapping for Acute Transvenous Phrenic Nerve Stimulation Study | Na | Sleep Apnea | Completed | 2013-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01913600 | Resolute Integrity US Extended Length Sub-Study(RI US XL) | Na | Coronary Artery Disease | Completed | 2013-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02234804 | The Does Optical Coherence Tomography Optimize Revascularization (DOCTOR) Recro… | Na | Coronary Disease | Unknown | 2013-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02180945 | ONYX Evaluation in the Endovascular Treatment of Intracranial Dural Arterioveno… | — | Arteriovenous Fistula | Completed | 2013-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01832493 | Sensor Optimization of Cardiac Resynchronization Therapy Response | Na | Heart Failure | Completed | 2013-07-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01905995 | Basal Ganglia Local Field Potentials in Gait and Speech | — | Basal Ganglia Diseases | Unknown | 2013-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01929902 | Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery | — | Cancer, Hepatocellular | Completed | 2013-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01917825 | A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in … | Phase2 | Sciatica | Completed | 2013-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01539161 | Reveal Chagas: Clinical Evidence of the Implantable Cardiac Monitor in Patients… | Phase4 | Chagas Disease | Terminated | 2013-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT03009175 | PRoMOTE Follow-up Observational Study | — | Heart Failure | Completed | 2013-06-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01874639 | Use of Transcollation Device to Decrease Blood Loss During Hepatic Resections: … | Phase2 | Hepatectomy | Unknown | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01882634 | Screening Programme for Abdominal Aortic Aneurysm by Hand-Held-Ultrasonography … | Early_Phase1 | Abdominal Aortic Aneurysm | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01946776 | Cardiac Arrhythmias in Epilepsy: the CARELINK-study | Na | Epilepsy | Completed | 2013-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01875016 | CRyo-Ablation to Treat Patients With HOCM. | Na | HOCM, Hypertrophic Obstructive Cardiomyopathy | Unknown | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01857973 | Overnight Closed Loop Study in U.S. | Na | Type 1 Diabetes | Completed | 2013-06-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01883141 | Left Ventricular MultiSpot Pacing for CRT (iSPOT) | Na | Heart Failure | Completed | 2013-06-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02146508 | Endoscopic Prevention of Esophageal Cancer at Tenwek Hospital | Na | Esophageal Cancer | Suspended | 2013-06-01 | 2024-07-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01712594 | Safety and Effectiveness Study of a Closed Loop System Maintaining Patients' Gl… | Na | Type 1 Diabetes | Completed | 2013-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01963039 | A Trial of Vertebroplasty for Painful Chronic Osteoporotic Vertebral Fractures … | Na | Osteoporosis | Completed | 2013-05-01 | 2020-09-03 | ClinicalTrials.gov |
| NCT01717014 | Radial Reload Open LAR Case Series | Na | Low Anterior Resection | Terminated | 2013-05-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01996397 | Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resyn… | Na | Heart Failure | Completed | 2013-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01779141 | Orchestra Pregnancy Observational Study in Poland | — | Type 1 Diabetes Mellitus | Completed | 2013-05-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01850901 | Renal Sympathetic Denervation as a New Treatment for Therapy Resistant Hyperten… | Phase3 | Hypertension | Completed | 2013-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01871519 | Evaluation of Outcomes for Quality of Life and Activities of Daily Living for B… | Na | Compression Fracture of Vertebral Body | Completed | 2013-05-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01989975 | CareLink Connect - Technical Evaluation Study | — | Diabetes Mellitus | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT03725826 | Risk Stratification After Acute Myocardial Infarction With Cardiac MRI | — | Acute Myocardial Infarction (AMI) | Completed | 2013-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01848184 | A Prospective Study in Patients Undergoing Primary Ventral Hernia Repair Using … | — | Hernia | Completed | 2013-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT02296008 | 3D High Resolution Anorectal Manometry in Children After Surgery for Anorectal … | Na | Children | Completed | 2013-04-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01818297 | Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients | Na | Failed Back Surgery Syndrome | Terminated | 2013-04-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01706822 | Radial Reload Laparoscopic LAR Case Series | Phase4 | Colorectal Cancer | Terminated | 2013-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02236507 | Normal Values for 3D High Resolution Anorectal Manometry in Children | Na | Children | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01921322 | Sensor Augmented Pump Therapy Versus Multiple Daily Injection Therapy | Na | Type 2 Diabetes | Completed | 2013-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01715116 | ENHANCED Device Programming to Reduce Therapies and Improve Quality of Life in … | Na | Cardiac Arrhythmias | Unknown | 2013-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01839695 | Safety and Efficacy of Valiant Mona LSA Stent Graft System | Na | Thoracic Aortic Aneurysms | Completed | 2013-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01841970 | Safety and Efficacy Study of HET Bipolar System for Treatment of Stage I and St… | Na | Hemorrhoids, Internal | Completed | 2013-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01823705 | Gastric Electrical Stimulation (GES) for the Treatment of Obesity | Na | Obesity | Completed | 2013-03-29 | 2017-01-13 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01775046 | Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment… | — | Aortic Aneurysm, Thoracic | Completed | 2013-03-23 | 2021-12-09 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01775059 | Collection of Performance Data From the Integrated Sensor and Infusion Set. TRI… | Na | Diabetes Mellitus Type I | Unknown | 2013-03-01 | — | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01808391 | A Prospective Multicenter Post Approval Study to Evaluate the Long-term Safety … | — | Coronary Artery Disease | Completed | 2013-03-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01735110 | PREPARE：Assessing the Safety and Efficacy of Radial Versus Femoral Approach PCI | Na | Transradial-transfemoral Coronary Interventions Comparison | Withdrawn | 2013-03-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01837537 | Respiration Rate V2.0 in a Hospital Setting | — | Respiratory Rate | Completed | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01522898 | Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrill… | Na | Heart Failure | Completed | 2013-03-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT01820390 | Optimizing DBS Electrode Placement and Programming | — | Parkinson's Disease | Withdrawn | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01726621 | User Evaluation of the MiniMed 620G and 640G Insulin Pumps | Na | Type 1 Diabetes | Completed | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01807585 | VenaSeal Sapheon Closure System Pivotal Study (VeClose) | Na | Great Saphenous Vein (GSV) With Venous Reflux Disease | Completed | 2013-03-01 | 2017-04-10 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01804062 | Respiration Rate V2.0 in Healthy Volunteers | — | Focus of the Study is Measuring Respiratory Rate | Completed | 2013-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01793376 | Development of Niv Score of Capsule Endoscopy in Patients With Crohn's (CECDAIi… | — | Crohn's Disease | Completed | 2013-02-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01112566 | EASE MITRAL Expertise-based Assessment Study on Clinical Efficacy of Profile 3D… | — | Mitral Valve Insufficiency | Completed | 2013-02-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01680835 | EverFlex Post Approval Study | Na | Peripheral Arterial Disease | Completed | 2013-01-14 | 2019-02-04 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01697358 | Spinal Cord Stimulation for Predominant Low Back Pain | Phase4 | Failed Back Surgery Syndrome | Completed | 2013-01-08 | 2017-06-20 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01832610 | Post- Approval Study on Patients Who Received a HeartWare HVAD® During IDE Tria… | — | Heart Failure | Completed | 2013-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01767558 | PRECISION GOLD Post Market Study in Europe of Pulmonary Vein Ablation Catheter … | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01804699 | National ARVC Data Registry and Bio Bank | — | Arrhythmogenic Right Ventricular Cardiomyopathy | Completed | 2013-01-01 | 2020-08-01 | ClinicalTrials.gov |
| NCT01779856 | Monitoring in Dialysis -- a Prospective, Multi-center, Single-arm, Non-randomiz… | Na | End Stage Renal Disease | Completed | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01778335 | Endovascular Treatment for Small Core and Proximal Occlusion Ischemic Stroke | Phase3 | Ischemic Stroke | Terminated | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01755416 | Liraglutide Versus Insulin Mono-therapy in the Closed Loop Setting | Phase2 | Type 1 Diabetes | Completed | 2013-01-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01772030 | Atrial Fibrillation Recurrence After Cryoballoon Ablation | Na | Atrial Fibrillation | Completed | 2013-01-01 | 2019-08-07 | ClinicalTrials.gov |
| NCT01929928 | Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System | — | Surgical Procedures, Operative | Completed | 2013-01-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01735916 | MIRACLE EF Clinical Study | Na | Congestive Heart Failure | Terminated | 2012-12-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01755143 | Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment | Na | Magnetic Resonance Imaging (MRI) | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01824160 | Pulmonary Artery Repair With Covered Stents | Na | Pulmonary Stenosis | Completed | 2012-12-01 | 2016-06-30 | ClinicalTrials.gov |
| NCT01995539 | Use of iPro™2 in Real Life Diabetes Management of Type 2 Patients in India | Na | Diabetes Mellitus, Type 2 | Completed | 2012-12-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01751022 | Attain Performa(TM) Quadripolar Lead Study | Na | Heart Failure | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01727297 | REVEAL AF: Incidence of AF in High Risk Patients | Na | Atrial Fibrillation | Completed | 2012-11-13 | 2017-01-30 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01750242 | Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Manageme… | — | Parkinson's Disease | Completed | 2012-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01609738 | Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the … | — | Left Ventricular Dysfunction | Completed | 2012-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01711619 | SubQStim: A Post-market Study of Subcutaneous Nerve Stimulation in Failed Back … | Na | Failed Back Surgery Syndrome | Terminated | 2012-11-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01747473 | Pulse Oximetry_Performance During Severe Signal Interference - PCBA-1 (Printed … | — | Healthy | Completed | 2012-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01796184 | Inflammation and Glycation in a General Adult Population | — | Inflammation | Completed | 2012-11-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01773668 | Feasibility Study - Integrated Sensor and Infusion Set. Trial III | Na | Type 1 Diabetes | Completed | 2012-11-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01692379 | Endovascular Revascularization With Solitaire Device Versus Best Medical Therap… | Phase3 | Acute Stroke | Terminated | 2012-11-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01736644 | Bipolar Sealer Aquamantys Use in Total Knee Replacement | Na | Osteoarthritis | Completed | 2012-10-01 | 2013-10-27 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01770561 | Feasibility Study of an Integrated Sensor and Infusion Set | Na | Diabetes Type 1 | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01762124 | Study of the Native Outflow Tract Transcatheter Pulmonary Valve (TPV) | Na | Congenital Heart Disease | Completed | 2012-10-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT01791582 | Pulse Oximetry- Evaluating Resp Rate- PCBA-1 | — | Healthy Subjects | Completed | 2012-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01706146 | Rhythm Evaluation for AntiCoagulaTion With COntinuous Monitoring | Phase4 | Atrial Fibrillation | Completed | 2012-10-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01683084 | Study of the Effectiveness of Telmisartan in Slowing the Progression of Abdomin… | Phase4 | Abdominal Aortic Aneurysm | Completed | 2012-09-19 | 2018-11-10 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01791569 | Pulse Oximetry- Evaluating Sensor Off- PCBA-1 | — | Healthy Subjects | Completed | 2012-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01719172 | A Prospective, Multi-Center, Single-Arm Study of the Veriset™ Hemostatic Patch … | Na | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | Completed | 2012-09-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01676727 | ADVANCE Direct Aortic Study | — | Aortic Stenosis | Completed | 2012-09-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01699529 | Multi-electrode Radiofrequency Renal Denervation System Feasibility Study | Na | Uncontrolled Hypertension | Completed | 2012-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02182947 | Capsule Endoscopy in Inflammatory Bowel Disease (IBD) in Children | Na | IBD | Completed | 2012-08-01 | 2018-12-30 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01675440 | Safety & Efficacy Study of the Medtronic CoreValve® System-Treatment of Symptom… | — | Severe Aortic Stenosis | Completed | 2012-08-01 | 2025-04-08 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01645917 | Durability of Pulmonary Vein Isolation Following Cryoablation for Treatment of … | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2012-08-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01720355 | Pulse Oximetry- Performance During Severe Signal Interference | — | Healthy Subjects | Completed | 2012-08-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01636648 | Enable I Long-term Follow-up Study | — | Aortic Valve Stenosis | Terminated | 2012-08-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01639833 | A Premarket, Prospective, Randomized, Single-Blind Study to Compare the Veriset… | Na | Cardiac Surgical Procedures | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01634269 | Clinical Evaluation of MDT-2111 in Subjects With Small Aortic Annuli and Sympto… | Na | Aortic Valve Stenosis | Completed | 2012-07-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01644604 | Renal Denervation by MDT-2211 System in Patients With Uncontrolled Hypertension | Na | Uncontrolled Hypertension | Completed | 2012-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT01638507 | An Evaluation of the Commercially Available Medtronic Resolute Integrity Zotaro… | Na | Coronary Artery Disease | Completed | 2012-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01557036 | Aneurysm Study of Pipeline in an Observational Registry | — | Brain Aneurysm | Terminated | 2012-06-21 | 2014-06-05 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01176617 | Assessing Arrhythmias After Ablation Using Implantable Recorders | Na | Atrial Fibrillation | Completed | 2012-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01521988 | Cryoballoon Pulmonary Venous Isolation in Patients Referred for Typical Atrial … | Na | Atrial Flutter | Completed | 2012-06-01 | 2018-04-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01626768 | Medtronic Market-Released DF4 Lead Imaging | — | Tachycardia | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01614262 | Examining The Role of CGM in T2DM | Na | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | Completed | 2012-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT02266407 | Surgical / Economic Effect of the Aquamantys System in Blood Management for Ase… | Na | Infection of Total Knee Joint Prosthesis | Completed | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01631435 | PillCam® Platform With the PillCam Crohn's Disease Capsule | Phase1 | Crohn's Disease | Completed | 2012-06-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01605500 | Utility of the Audible Alert in Current Generation Medtronic Implantable Cardio… | — | Patients With a Generation 2 Medtronic Implantable Cardioverter-defibrillator(ICD) | Completed | 2012-06-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01609296 | IN.PACT Global Clinical Study | Na | Peripheral Arterial Disease | Completed | 2012-05-01 | 2020-01-17 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01426425 | Intracardiac CrYoablation for AtrioVentricular Nodal Reentrant Tachycardia | Phase3 | AtrioVentricular Nodal Reentrant Tachycardia | Completed | 2012-05-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01850498 | Epilepsy Motion Sensing | — | Epilepsy | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01520506 | Rapid Renal Sympathetic Denervation for Resistant Hypertension | Na | Hypertension, Resistant to Conventional Therapy | Completed | 2012-05-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01534819 | ANCHOR (Aneurysm Treatment Using the Heli-FX™ EndoAnchor™ System Global Registr… | — | Aortic Aneurysm | Completed | 2012-04-01 | 2026-04-08 | ClinicalTrials.gov |
| NCT01660035 | The Product Surveillance Registry REVERSE Post Approval Study | — | Heart Failure | Completed | 2012-04-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT01308996 | Clinical Study of INFUSE® Bone Graft Compared to Autogenous Bone Graft for Vert… | Na | Alveolar Bone Loss in Mandible | Withdrawn | 2012-04-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT01718249 | Study of Conscious Behavior Under Low-frequency Deep Brain Stimulation in Chron… | Na | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | Completed | 2012-04-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01754194 | Clinical and Economic Outcomes in Laparoscopic Sleeve Gastrectomy Versus Roux-e… | — | Morbid Obesity | Completed | 2012-04-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01539135 | The Influence of Endotracheal Tube Design on Fluid Leakage Into the Lungs Durin… | Na | Respiratory Aspiration | Completed | 2012-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01590940 | Use of Parietex Plug and Patch Hernia System in Open Inguinal Hernia Repair | — | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | Unknown | 2012-04-01 | — | ClinicalTrials.gov |
| NCT03125382 | PORTuguese Research on Telemonitoring With CareLink® (PORTLink) | Na | Arrhythmia | Completed | 2012-04-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01586910 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Active_Not_Recruiting | 2012-04-01 | 2026-11-01 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01521754 | Product Surveillance Registry- Deep Brain Stimulation for Epilepsy | — | Refractory Epilepsy | Completed | 2012-03-06 | 2019-06-19 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01526811 | Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic A… | — | Aneurysm | Completed | 2012-03-01 | 2018-12-21 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01575093 | Safety Evaluation of Bowel Cleansing Regimen for PillCam® COLON 2 Capsule Endos… | Phase1 | Healthy Volunteers | Completed | 2012-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01763567 | Feasibility Study to Evaluate Safety and Device Performance of the Hospital Glu… | — | Hyperglycemia | Completed | 2012-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01520532 | Evaluation of the Incidence of Cerebral Lesions Post Pulmonary Vein Ablation Ca… | Na | Atrial Fibrillation | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01558102 | International Retrospective Study of Pipeline Embolization Device | — | Brain Aneurysms | Completed | 2012-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01531374 | Safety and Efficacy Continued Access Study of the Medtronic CoreValve® System i… | Na | Severe Aortic Stenosis | Completed | 2012-02-21 | 2019-11-18 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01503476 | Development of Applications of the Bravo® pH Monitoring System and Evaluation o… | Phase4 | Gastro Esophageal Reflux Disease | Completed | 2012-02-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01548222 | CGM Evaluation of Glucose Excursions in Basal Insulin Treated T2DM at Fasting G… | — | Type 2 Diabetes | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01845909 | Sudden Cardiac Death - Screening Of Risk Factors | — | Sudden Cardiac Death | Unknown | 2012-02-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01761448 | Heart Cycle GEx (Guided- Exercise- Main Trial) | Na | Coronary Artery Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01534299 | Global SYMPLICITY Registry (GSR) DEFINE | — | Hypertension | Recruiting | 2012-02-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01562912 | Efficiency Study Evaluating the Use of PVAC Catheter Technology for Performing … | Na | Atrial Fibrillation | Completed | 2012-02-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT01511939 | Trial to See if Topical Pennsaid for Knee Pain Affects Coagulation Values in Pa… | Phase3 | Osteoarthritis of the Knee | Completed | 2012-02-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01638897 | DF4 Connector System Post-Approval Study | — | Ventricular Tachycardia | Completed | 2012-01-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01531426 | Cerebral Oxygenation in Cardiac Arrest and Hypothermia | — | Cardiac Arrest | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01778426 | Post-reimbursement Study to Follow Spinal Neurostimulator Devices for Pain Ther… | — | Chronic Pain Syndrome | Completed | 2012-01-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT03723265 | Personalized CRT - PSR | — | Heart Failure | Completed | 2012-01-01 | 2022-04-28 | ClinicalTrials.gov |
| NCT01524276 | Product Surveillance Registry | — | Cardiac Rhythm Disorders | Recruiting | 2012-01-01 | 2040-01-01 | ClinicalTrials.gov |
| NCT01552109 | Stable Angina Observational Registry | — | Stable Angina | Completed | 2012-01-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01454700 | Effect of CSII and CGM on Progression of Late Diabetic Complications | Phase4 | Type 1 Diabetes Mellitus | Completed | 2011-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01509495 | Impedance Measurements in Heart Failure Patients | Phase1 | Heart Failure | Terminated | 2011-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01565967 | Registry AutoLog Lipid Removal and Blood Component Characterization | — | Trauma | Completed | 2011-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01570101 | European Sapheon™ Closure System Observational ProspectivE (eSCOPE) Study | Na | Venous Insufficiency of Leg | Completed | 2011-12-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01350622 | Efficacy of PENNSAID® for Pain Management in the Emergency Department | Na | Pain | Withdrawn | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01497938 | Outpatient Study to Evaluate Safety and Effectiveness of the Low Glucose Suspen… | Phase3 | Type 1 Diabetes | Completed | 2011-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01490814 | FIRE AND ICE: Comparative Study of Two Ablation Procedures in Patients With Atr… | Na | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | Completed | 2011-12-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01459627 | Randomized, Open Label Trial of 6 Months Versus 12 Months DAPT After Drug-Eluti… | Phase4 | Myocardial Infarction | Completed | 2011-12-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01599065 | Comparison of a MAGNET Protocol Versus "off-on" Protocol for Patients With Impl… | — | Sudden Cardiac Death | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01490151 | Medtronic Treat to Range (TTR) Closed-Loop Control | Na | Diabetes Mellitus | Completed | 2011-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT01776749 | Subcutaneous Stimulation as Add on Therapy to SCS toTreat Low Back Pain in FBSS | Na | Low Back Pain | Completed | 2011-11-09 | 2015-07-11 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01095952 | AV-node Stimulation Clinical Download Study to Reduce Ventricular Rate During AF | Na | Atrial Fibrillation | Completed | 2011-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01462968 | Interruptions in the Coagulationsystem in Relation With Cardiac Surgery - A Stu… | Na | Cardiac Surgery | Withdrawn | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01721369 | Applicability of Syncope Guidelines in Cataluña | — | Brief Loss of Consciousness | Completed | 2011-11-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01475175 | Adaptive Cardiac Resynchronization Therapy Optimization at Rest and During Exer… | Na | Heart Failure | Terminated | 2011-11-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02027909 | A Comparison of Rate Response Performance in Pacemaker Patients With an Indicat… | — | Sinus Node Dysfunction | Completed | 2011-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02060357 | Comparison of Two New Generation Drug Eluting Stents in Patients With Diabetes … | Na | Coronary Artery Disease | Completed | 2011-11-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01461434 | Graz Study on the Risk of Atrial Fibrillation | Phase4 | Atrial Fibrillation | Unknown | 2011-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01509378 | 4P Study: Predictive Quality With Painfree Therapies | — | Cardiac Arrhythmias | Completed | 2011-11-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01392196 | Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Cli… | Na | Heart Failure | Terminated | 2011-10-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01458483 | Acute Carotid Sinus Endovascular Stimulation II Study | Phase1 | Hypertension | Completed | 2011-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01481376 | TAPP Inguinal Hernia Repair With Self-fixating Parietex™ ProGrip™ Mesh | — | Postoperative Complications | Completed | 2011-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01395836 | Management of New-Onset Postoperative Atrial Fibrillation | — | Atrial Fibrillation | Completed | 2011-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02989363 | Evaluation of the Use of Resources and Costs | Na | Surgical Incision | Unknown | 2011-10-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01448382 | Evaluation of PillCam With Blood-Sensing Feature: A Feasibility Study | Phase1 | Upper GI Bleeding | Terminated | 2011-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01348438 | Transapical Implantation of the Medtronic Engager Transcatheter Aortic Valve Im… | Na | Aortic Valve Stenosis | Completed | 2011-09-12 | 2018-01-25 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01334268 | RESOLUTE China RCT | Na | Ischemic Heart Disease | Completed | 2011-09-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01448265 | Real-Time Assessment of Cryoballoon Pulmonary Vein Isolation Using a Novel Circ… | Phase4 | Atrial Fibrillation | Completed | 2011-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01512121 | Spinal Cord Stimulation and Functional MRI | — | Complex Regional Pain Syndrome (CRPS) | Completed | 2011-09-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01781715 | Multivessel Stenting Versus Staged Revascularization With Zotarolimus-eluting S… | Phase4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | Unknown | 2011-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01370759 | Feasibility Study to Evaluate the Performance of Flocculation-Adsorption System… | Phase1 | Healthy | Terminated | 2011-09-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01759550 | Prospective Case-Series of Ligasure Advance Pistol Grip and LigaSure Blunt Tip | — | Morbid Obesity | Terminated | 2011-09-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01458262 | Observational Study on the Clinical Impact of Desaturation During Liver Surgery | — | Cerebral Desaturation | Completed | 2011-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01446796 | Right Ventricular (RV) Pacing in Early Post-operative Continuous Flow Left Vent… | Phase4 | Heart Failure | Terminated | 2011-09-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01514773 | Patient and Physician Survey Determinants of Appropriate ICD Utilization | — | Heart Failure, Systolic | Completed | 2011-08-01 | 2013-08-30 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01561144 | UMBRELLA - Incidence of Arrhythmias in Spanish Population With a Medtronic Impl… | — | Cardiomyopathies | Terminated | 2011-08-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01850706 | UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neurom… | — | Detrusor Overactivity | Completed | 2011-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01406236 | SAFE-PCI for Women | Na | Percutaneous Coronary Intervention | Terminated | 2011-08-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01433042 | PillCam SB3 Capsule- Feasibility Study | Na | Small/Large Bowel | Completed | 2011-08-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01656954 | Predicting Volume Response Study | — | Shock | Completed | 2011-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01807338 | A Follow-up Study on Safety and Tolerability of Intracerebroventricular Adminis… | — | Parkinson's Disease | Completed | 2011-08-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02111993 | Evaluating Myocardial Injury for Defibrillation Threshold Testing Methods for I… | Na | Cardiomyopathy | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01379222 | Endurant Stent Graft System Post Approval Study (ENGAGE PAS) | Na | Aortic Aneurysm, Abdominal | Completed | 2011-08-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02492243 | Continuous Rhythm Monitoring in Patients After Acute Myocardial infaRction andp… | Phase2 | Myocardial Infarction | Completed | 2011-08-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01366482 | Atherectomy Followed by a Drug Coated Balloon to Treat Peripheral Arterial Dise… | Na | Peripheral Arterial Disease | Completed | 2011-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01392846 | The IRIS-Resolute Integrity (IRIS-Integrity) | — | Coronary Artery Disease | Completed | 2011-07-01 | 2020-03-02 | ClinicalTrials.gov |
| NCT01603433 | The Sapheon Closure System Feasibility Study | Na | Venous Insufficiency of Leg | Completed | 2011-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01362465 | Characterization of Interventricular Conduction Measurements | Early_Phase1 | Heart Failure | Completed | 2011-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01058551 | Incidence of Atrial Fibrillation in Patients With Severe Obstructive Sleep Apne… | Na | Obstructive Sleep Apnea | Completed | 2011-06-01 | 2019-09-18 | ClinicalTrials.gov |
| NCT01321073 | DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study | Na | Pulmonary Arterial Hypertension | Active_Not_Recruiting | 2011-06-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01370564 | Feasibility of an Integrated Patient Care (IPC) System Using Daily Filling Pres… | Phase2 | Heart Failure | Completed | 2011-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01372878 | Evaluation of Capsule Endoscopy With PillCam® COLON 2 in Visualization of the C… | Na | CRC Screening | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01526629 | Full Automaticity and Remote Follow-up | — | Tachyarrhythmia | Completed | 2011-05-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01522755 | Predictive Factors of a Successful Implant of the CapsureFix MRI Model 5086 | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01513538 | Analysis of the Acceptance and Changes to Parameters Programming Suggested by t… | — | Bradyarrhythmia | Completed | 2011-05-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01415024 | Resynchronization in Paced Heart Failure Patients With Implantable Cardioverter… | Phase4 | Heart Failure | Unknown | 2011-05-01 | — | ClinicalTrials.gov |
| NCT01361685 | Model 4396 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2021-02-04 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01366703 | Optimized Heart Failure Therapy Through Continuous Monitoring | — | Heart Failure | Unknown | 2011-05-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01361672 | Model 4296 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2011-05-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01412463 | DURABILITY+ : a Prospective, Multi-center, Controlled Study With the Everflex+ … | Phase4 | Peripheral Arterial Disease | Completed | 2011-05-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01404351 | Use of the PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia (Symptomatic) | Withdrawn | 2011-05-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT00673842 | Efficacy of Implantable Defibrillator Therapy After a Myocardial Infarction | Phase3 | Myocardial Infarction | Completed | 2011-04-18 | 2024-10-31 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00698139 | Cardiovascular and Neurohormonal Effects of Faster Atrial Pacing Rate | Na | Heart Failure | Terminated | 2011-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01341483 | Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study | — | Erectile Dysfunction Due to Arterial Insufficiency | Terminated | 2011-04-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01360008 | FREEZE Cohort Study | — | Arrhythmia | Completed | 2011-04-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01325935 | Optimal Duration of DAPT Following Treatment With Endeavor (Zotarolimus-eluting… | Phase4 | Coronary Artery Disease | Completed | 2011-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01277783 | ALternate Site Cardiac ReSYNChronization (ALSYNC) Study | Na | Heart Failure | Completed | 2011-03-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01956448 | SORT-OUT VI - Randomized Clinical Comparison of Biomatrix Flex® and Resolute In… | Na | Coronary Artery Disease | Completed | 2011-03-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00399594 | Effect of Targeting Left Ventricular Lead Position on the Rate of Response to C… | Phase2 | Heart Failure, Congestive | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01308164 | MD Logic Pump Advisor -Pediatric Study | Na | Type 1 Diabetes | Completed | 2011-03-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01299675 | SureScan Post-Approval Study | — | Bradycardia | Completed | 2011-02-08 | 2017-10-02 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01268514 | ENHANCE: A Prospective EvaluatioN of Permacol™ in tHe Repair of Complex AbdomiN… | — | Hernia, Abdominal | Completed | 2011-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01294514 | Novel Non-Invasive Monitoring Parameter in Healthy Volunteers | — | No Conditions | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01216670 | Cardiac Rhythm Monitoring After Acute Decompensation for Heart Failure | — | Heart Failure | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01324349 | Comparison of the Hemostatic Patch to Fibrin Sealant (TachoSil®) in Subjects Un… | Na | Liver Disease | Completed | 2011-02-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01297335 | Effect of Intrathecal Clonidine in Hypertensive Subjects With Poorly Controlled… | Phase2 | Hypertension | Completed | 2011-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01308554 | Pain Relieving Efficacy of TAP Block in Patients After Laparoscopic Gastric Byp… | Phase4 | Pain | Completed | 2011-02-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01355835 | Combined STN/SNr-DBS for the Treatment of Refractory Gait Disorders in Parkinso… | Phase2 | Parkinson's Disease | Completed | 2011-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01306201 | Novel Non-Invasive Monitoring Parameter in a Hospital Setting | — | Respiratory Insufficiency | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT02027883 | Comparison of VF Induction Techniques During Medtronic ICD Implant (VF) (ICD) | Na | Cardiomyopathy | Completed | 2011-01-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01284491 | A Study to Evaluate Cutaneous Scar Quality Following Bilateral Breast Reduction… | Na | Macromastia | Terminated | 2011-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01267318 | Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure | — | Gastrointestinal Bleeding | Terminated | 2011-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01242397 | Mitral Insufficiency Reduction With Biventricular Pacing | Phase1 | Mitral Regurgitation | Unknown | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01026025 | Duet TRS Used in Pulmonary Resections | Na | Lung Cancer | Withdrawn | 2011-01-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01306877 | Comparison Study of Surgical Staplers for the Treatment of Hemorrhoids | Na | Hemorrhoids | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01240902 | Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment o… | Na | Severe Aortic Stenosis | Completed | 2010-12-10 | 2019-05-15 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01264484 | ADVANTAGE® Prosthetic Heart Valve Long-term Follow-up Trial | — | Heart Valve Stenosis | Terminated | 2010-12-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01243749 | RESOLUTE China Registry: | — | Ischemic Heart Disease | Completed | 2010-12-01 | 2017-12-15 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01269372 | Evaluation of Capsule Endoscopy With PillCam® Colon 2 in Visualization of the C… | Na | Colorectal Lesions | Completed | 2010-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01182493 | OpT2mise Glucose Control in Type 2 Diabetes Mellitus (DM) With Insulin Pump The… | Na | Diabetes Mellitus, Type 2 | Completed | 2010-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01213251 | Post-Myocardial Infarction Remodeling Prevention Therapy | Phase2 | Acute Myocardial Infarction | Completed | 2010-12-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01905007 | Study of Defibrillation Testing In Patients Undergoing Initial ICD Implantation | Phase4 | Ventricular Arrhythmias | Unknown | 2010-12-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01241565 | ENDO GIA™ Stapler With ENDO GIA™ Reload With Tri-Staple™ Technology in a Pulmon… | Na | Lung Cancer | Completed | 2010-11-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01219894 | Intravascular Optical Coherence Tomography Imaging - Length of Anti-Platelet Th… | — | Coronary Artery Disease | Withdrawn | 2010-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01664806 | Laparoscopic Cholecystectomy And Capacitive Coupling - Coag Versus Blend Mode C… | Phase3 | Intraoperative Complications | Completed | 2010-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00918125 | Educational Videos to Improve Patient Decision Making and Race Disparities in I… | — | Sudden Cardiac Arrest | Completed | 2010-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01174186 | Intestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab… | Phase4 | Spondyloarthritis | Completed | 2010-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01236365 | Statins in Children With Type 1 Diabetes and Hypercholesterolemia | Phase3 | Diabetes Mellitus, Insulin-Dependent | Completed | 2010-10-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01214252 | A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Re… | — | Abdominal Wall Defects | Completed | 2010-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01233310 | Evaluation of Small Bowel Colon Capsule for Bowel Visualization in Crohn's Dise… | — | Crohn Disease | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01327989 | Solitaire FR Thrombectomy for Acute Revascularisation | — | Stroke, Acute | Completed | 2010-10-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01231308 | Roux-en-Y-Gastric Bypass vs. Lifestyle Modification and Medical Therapy in the … | Na | Type 2 Diabetes | Unknown | 2010-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01151631 | Occipital Nerve Stimulation in Medically Intractable Chronic Cluster Headache | Phase3 | Chronic Cluster Headache | Completed | 2010-10-01 | 2019-03-01 | ClinicalTrials.gov |
| NCT01223547 | Study of the Effects of Carbohydrate Counting | Na | Type 1 Diabetes | Completed | 2010-10-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01515761 | POsition of Leads in Advanced heaRt Failure: the POLAR Study | Na | Cardiac Resynchronization Therapy | Unknown | 2010-09-01 | — | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01349426 | Ligasure II: Standard Stapling Versus Ligasure | Phase3 | Lung Resection | Terminated | 2010-09-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01175850 | Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for th… | Na | Peripheral Arterial Disease (PAD) | Completed | 2010-09-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01059175 | Dual-Site LV Pacing in CRT Non Responders: Multicenter Randomized Trial | Na | Heart Failure | Completed | 2010-09-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01204281 | Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients | Phase4 | Respiratory Failure | Completed | 2010-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01194388 | Axium Coil in Completing Endovascular Aneurysm Surgery Study | — | Intracranial Aneurysm | Withdrawn | 2010-09-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01276249 | The STAPLE International Post-Market Registry | — | Aortic Aneurysm, Abdominal | Terminated | 2010-08-01 | 2015-06-19 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01166347 | The HeartWare™ Ventricular Assist System as Destination Therapy of Advanced Hea… | Na | Chronic Heart Failure | Completed | 2010-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02051621 | Therapy of Atrial Flutter by Afib Ablation | Na | Atrial Fibrillation | Unknown | 2010-08-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01394588 | Continuous Glucose Monitoring Technology in the Perioperative Period During Car… | — | Cardiac Surgery | Withdrawn | 2010-08-01 | — | ClinicalTrials.gov |
| NCT01168427 | Reveal In-Office Implants | — | Arrhythmias, Cardiac | Completed | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01110538 | The Massachusetts General Hospital Optical Coherence Tomography Registry | — | Coronary Artery Disease | Completed | 2010-08-01 | 2019-04-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01157923 | MD Logic Pump Advisor- Adults Study | Na | Type 1 Diabetes | Completed | 2010-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01161043 | New Glucose Sensor Pediatric | Na | Type 1 Diabetes Mellitus | Completed | 2010-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01054534 | Ultrasound Image Fusion for Placement of Sacral Quadripolar Leads | Na | Urinary Incontinence | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01169311 | Safety and Performance of the Covidien EEA Hemorrhoid and Prolapse Stapling Set… | Na | Hemorrhoid | Completed | 2010-07-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01297283 | Leadless Electrocardiogram (ECG) Evaluation Study | Na | Heart Failure | Completed | 2010-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01163422 | Right Ventricular Resynchronization Therapy | Na | Right Ventricular Failure | Unknown | 2010-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01175278 | Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body … | Na | Multiple Myeloma | Withdrawn | 2010-07-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01714921 | Protecta Smart Analysis Register | — | Patients With an Indication for an ICD Implantation According to the Guidelines | Completed | 2010-06-09 | 2015-01-05 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01110915 | Advisa MRI Clinical Study | Na | Magnetic Resonance Imaging | Completed | 2010-06-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01150500 | RESOLUTE Japan SVS: The Clinical Evaluation of the MDT-4107 DES in the Treatmen… | Na | Arterial Occlusive Diseases | Completed | 2010-06-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01143324 | A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal … | — | Degenerative Lumbar Spine Causing Back and/or Leg Pain | Completed | 2010-06-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01117090 | Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who H… | — | Cerebral Palsy | Completed | 2010-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01156272 | Post Market ATS 3f® Aortic Bioprosthesis, Model 1000, Size 19mm | — | Heart Valve Diseases | Withdrawn | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01081886 | PEAK PlasmaBlade 4.0 Versus Traditional Electrosurgery in Total Knee Replacemen… | Na | Degenerative Joint Disease | Terminated | 2010-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01480635 | PillCam Colon 2 Capsule Endoscopy (PCCE) After Incomplete Colonoscopy | — | Colonoscopy | Unknown | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01128036 | Comparison of Different Locations for Pulse Oximetry Probes in Cardiovascular (… | — | Congestive Heart Failure | Terminated | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00997516 | Single-incision Laparoscopic (SILS) Versus Conventional Laparoscopic Appendecto… | Na | Appendicitis | Terminated | 2010-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01114724 | Study to Evaluate the Clinical Performance of the Valiant Thoracic Stent Graft … | Na | Aortic Dissection | Completed | 2010-05-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01217827 | Implantable Cardioverter-Defibrillator Use in the VA System | Phase3 | Cardiomyopathies | Completed | 2010-04-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01129609 | Talent Converter Post-Approval Study | — | Abdominal Aortic Aneurysms | Terminated | 2010-04-01 | 2017-09-29 | ClinicalTrials.gov |
| NCT01092767 | Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating… | Na | Blunt Thoracic Aortic Injury | Completed | 2010-04-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01135745 | Deep Brain Stimulation for Obsessive Compulsive Disorder (OCD PMCF) | Phase4 | Obsessive Compulsive Disorder | Completed | 2010-04-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01112696 | An Inpatient Performance Evaluation of a New Subcutaneous Glucose Sensor | Na | Type 1 Diabetes Mellitus | Completed | 2010-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01113372 | Optimized Duration of Clopidogrel Therapy Following Treatment With the Endeavor… | Phase4 | Coronary Artery Disease | Completed | 2010-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01108640 | Continuous Glucose Monitoring in Critically Ill Surgical Patients | — | Hyperglycemia | Completed | 2010-04-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01323439 | Axium™ MicroFX™ for Endovascular Repair of IntraCranial Aneurysm-A Multicenter … | — | Aneurysm | Completed | 2010-04-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01110109 | Removing Fluid Above Breathing Tubes in the Operating Room | — | Pneumonia, Ventilator-Associated | Completed | 2010-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01109771 | Absorbable Versus Permanent Mesh Fixation Trial in Laparoscopic Midline Ventral… | Na | Ventral Hernia | Completed | 2010-04-01 | 2015-08-31 | ClinicalTrials.gov |
| NCT01112579 | Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of… | Phase2 | Heart Failure | Completed | 2010-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01045343 | Feasibility Study of an Integrated Diagnostic System to Manage Heart Failure | Na | Heart Failure | Completed | 2010-03-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01074658 | CoreValve Advance International Post Market Study | — | Severe Aortic Stenosis | Completed | 2010-03-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01068119 | Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplast… | Phase4 | Acute Coronary Syndrome | Terminated | 2010-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01195285 | Single-Incision Laparoscopic Cholecystectomy Versus Traditional Laparoscopic Ch… | Na | Biliary Dyskinesia | Terminated | 2010-02-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01006070 | Health-Related Quality of Life (QOL), Physical and Respiratory Function in Pati… | — | Multiple Myeloma | Completed | 2010-02-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01082575 | Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor | — | Sleep Disordered Breathing | Completed | 2010-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01077947 | Value of Functional Anesthetic and Provocative Discography in the Surgical Trea… | Phase4 | Discogenic Pain | Withdrawn | 2010-02-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01181947 | VALIANT CAPTIVIA Post-market Registry | — | Aortic Aneurysm, Thoracic | Terminated | 2010-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01109641 | PhrenIc Nerve mappinG and Stimulation EP Catheter Study: PING-EP Study | Phase4 | Heart Failure | Completed | 2010-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT02023775 | Non Interventional Study on Pulmonary Valve Replacement by Thranscatheter Pulmo… | — | Right Ventricular Congenital Cardiopathies | Completed | 2010-01-31 | 2013-10-20 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00905359 | Neurogenic Intermittent Claudication Evaluation Study | Phase4 | Spinal Stenosis | Completed | 2010-01-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01026103 | Tri Staple Technology Stapler Used in Gastric Bypass | Na | Sleep Apnea | Completed | 2010-01-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01054560 | SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study | Na | Ischemic Stroke | Completed | 2010-01-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01023022 | CareLink® Network Evaluation | — | Heart Failure | Completed | 2010-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01044602 | Metabolic Surgery Versus Medical Management for Resolution of Type II Diabetes | Na | Obesity | Completed | 2010-01-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00986453 | PEAK PlasmaBlade 4.0 in Bilateral Breast Reduction | Na | Macromastia | Completed | 2010-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01085539 | Oxygen Saturation Alarms in the Neonatal Intensive Care Unit | — | Hypoxemia | Completed | 2010-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01023269 | Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Over… | Na | Neurogenic Overactive Bladder | Terminated | 2009-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01334866 | Graft Patency Outcomes in Patients Undergoing Coronary Artery Bypass Grafting V… | Phase4 | Arteriosclerosis of Coronary Artery Bypass Graft | Completed | 2009-12-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01520714 | Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds … | Na | Congestive Heart Failure | Terminated | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01032577 | A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurati… | — | Ischemic and Nonischemic Cardiomyopathy, With Primary and Secondary Implant Indications | Completed | 2009-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01032239 | SISTERS: Spasticity In Stroke Study - Randomized Study | Phase4 | Severe Spasticity | Completed | 2009-11-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00940056 | Totally Endoscopic Ablation of Atrial Fibrillation | Na | Atrial Fibrillation | Completed | 2009-11-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01009333 | InterStim Therapy Programming Study | Na | Urgency Frequency | Completed | 2009-11-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00950872 | Safety and Efficacy Study of Duet TRS | Na | Roux En Y Gastric Bypass | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01583465 | Efficacy of Aquamantys for Reducing Transfusions With Anterior Supine Intermusc… | Na | Osteoarthritis, Hip | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00977938 | The Dual Antiplatelet Therapy Study (DAPT Study) | Phase4 | Coronary Artery Disease | Completed | 2009-10-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00991432 | Localized Alveolar Ridge Augmentation With Space Maintenance Devices | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00991393 | Sinus Augmentation With Dental Implant | — | Maxillary Sinus Bone Loss | Terminated | 2009-10-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00991965 | Localized Alveolar Ridge Augmentation With Dental Implant | — | Alveolar Bone Loss | Terminated | 2009-10-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00942474 | Nerve Access Tool Study | Na | Cystocele | Withdrawn | 2009-10-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00991120 | Extension Phase of the Chronicle® Offers Management to Patients With Advanced S… | — | Heart Failure | Completed | 2009-10-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01088646 | Evaluation of PillCam® Express Capsule Endoscopy Delivery System | Na | Small Bowel Disease | Completed | 2009-10-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00980057 | Adaptive Cardiac Resynchronization Therapy Study | Na | Heart Failure | Completed | 2009-10-01 | 2012-03-08 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT00941733 | Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treat… | Na | Critical Lower Limb Ischemia | Completed | 2009-09-01 | 2017-11-30 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00949676 | DECIDE-HF: Heart Rate Variability in Heart Failure Patients | — | Systolic Heart Failure | Unknown | 2009-09-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00998374 | Comparison Between Pyloric Preserving and Non-Pyloric Preserving Bariatric Surg… | — | Hypoglycemia | Completed | 2009-09-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01116037 | ATS 3f(r) Aortic Bioprosthesis Model 1000 Post Approval Study | Na | Heart Valve Diseases | Terminated | 2009-09-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01063231 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2009-09-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00982397 | Safety and Clinical Performance of the Protecta ICD and CRT-D | Na | Tachyarrhythmias | Completed | 2009-09-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00990782 | Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment | Na | Esophageal Lesion | Completed | 2009-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00963781 | Scripps Evaluation of Antiplatelet Therapies for Intermediate Duration With the… | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00974701 | A Pilot and Feasibility Study to Evaluate Capsule Endoscopy | Na | Upper Gastrointestinal Hemorrhage | Completed | 2009-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00961311 | Sprinter Legend Balloon Catheter | Na | Coronary Artery Disease | Completed | 2009-08-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00959374 | Evaluation of Dermal Closure With an Absorbable Barbed Suture as Compared to a … | Na | Breast Ptosis | Completed | 2009-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01037426 | Falls and Cardiovascular Events in Pacemaker Patients | Phase4 | Bradycardia | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01091740 | ComparisiOn of Neointimal coVerage betwEen ZES and EES Using OCT at 3 Months | Phase4 | Coronary Artery Disease | Completed | 2009-08-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00820040 | Feasibility of Permacol Use in Infected Fields | Phase2 | Hernia | Terminated | 2009-07-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00952458 | Bispectral Index Monitoring of Sedation During Endoscopic Retrograde Cholangiop… | Na | Gastrointestinal Endoscopy | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01087528 | Evaluation of PillCam™ Colon 2 in Visualization of the Colon | Na | Colonic Diseases | Completed | 2009-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00893386 | Attain StarFix® 4195 Lead Extraction Study | — | Heart Failure | Completed | 2009-07-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00998660 | RECHARGE Sub-Study to the Implantable Systems Performance Registry (ISPR) | Phase4 | Parkinson's Disease | Completed | 2009-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00960154 | PEAK PlasmaBlade™ 4.0 Versus Traditional Electrosurgery in Lumpectomy | Na | Breast Cancer | Terminated | 2009-07-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01098851 | Oxygen Saturation Monitoring During Surgery | — | Sleep Apnea, Obstructive | Completed | 2009-07-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00924638 | Study of Continuous Cardiac Monitoring to Assess Atrial Fibrillation After Cryp… | Phase4 | Cryptogenic Symptomatic Transient Ischemic Attack | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT01074671 | CG Future® Annuloplasty Ring/Band Clinical Trial | Phase4 | Mitral Valve Insufficiency | Completed | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01384162 | An Open Label, Safety and Tolerability Continuation Study of Intracerebroventri… | Phase1 | Amyotrophic Lateral Sclerosis | Terminated | 2009-06-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01039467 | A Comparison of the Pacemaker Automatic Features in Reduction of Ventricular Pa… | Na | Bradycardia | Completed | 2009-06-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00885677 | MOnitoring REsynchronization deviCes and cARdiac patiEnts | Na | Heart Failure | Terminated | 2009-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00922402 | Heart & Diabetes - Feasibility Study | Na | Acute Heart Failure | Withdrawn | 2009-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00944125 | Dual Site Left Ventricular (LV) Pacing | Na | Congestive Heart Failure | Terminated | 2009-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00932659 | Continuous Cardiac Arrhythmia Monitoring in Hemodialysis Patients | — | Arrhythmias, Cardiac | Completed | 2009-06-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00930904 | Model 4196 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-06-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01369823 | Diabetes Multicenter Observational Study (DIAMOND-1-) | — | Diabetes | Unknown | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00926718 | The Effect of Rocuronium on the Response of Composite Variability Index (CVI) t… | Na | Laryngoscopy | Unknown | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00888433 | Renal Denervation in Patients With Uncontrolled Hypertension (Symplicity HTN-2) | Na | Uncontrolled Hypertension | Completed | 2009-06-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00927251 | Model 4296 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01450813 | The Effect of Neuromuscular Blockade on the Composite Variability Index (CVI) D… | Na | Anesthesia | Completed | 2009-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00919633 | Safety and Efficacy Study to Compare Continuous Infusion of Interferon With Sta… | Phase2 | Hepatitis C | Completed | 2009-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT00877643 | Routine Versus Aggressive Upstream Rhythm Control for Prevention of Early Atria… | Na | Atrial Fibrillation | Completed | 2009-05-04 | 2021-01-31 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00887237 | Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT)… | Phase3 | Heart Failure | Completed | 2009-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00898768 | Capsule Endoscopy to Screen for Small Bowel Neoplasia in Lynch Syndrome | Early_Phase1 | Lynch Syndrome | Completed | 2009-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01186094 | Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-… | Phase4 | Coronary Artery Disease | Completed | 2009-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00913601 | Treatment of Faecal Incontinence With Sacral Nerve Stimulation - Improved Funct… | Na | Fecal Incontinence | Terminated | 2009-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00870051 | Endurant Stent Graft Natural Selection Global Postmarket Registry | — | Aortic Aneurysm, Abdominal | Completed | 2009-04-08 | 2021-09-23 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00805948 | Post-Approval Clinical Study of the Talent Thoracic Stent Graft to Treat Thorac… | Na | Thoracic Aortic Aneurysms | Terminated | 2009-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00832767 | SILS™ Port Laparoscopic Cholecystectomy Post Market Study | Na | Gallbladder Disease | Completed | 2009-04-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00919672 | Treatment of Irritable Bowel Syndrome (IBS) With Sacral Nerve Stimulation | Na | Irritable Bowel Syndrome | Completed | 2009-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00856349 | Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programm… | — | Cardiovascular Disease | Completed | 2009-04-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00884624 | Evaluation of the PillCam™ Colon Capsule -2 System | — | Bowel Diseases | Completed | 2009-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01666054 | Comparison of Weaning on Pressure Support vs. Proportional Assist Ventilation: … | Na | Weaning From Mechanical Ventilation | Completed | 2009-03-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01156662 | Efficacy of Thrombosuction in Primary Percutaneous Coronary Intervention of Acu… | Phase4 | Acute Myocardial Infarction | Unknown | 2009-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01169454 | Ventriculostomy in Subarachnoid Hemorrhage (SAH): Intracranial Pressure (ICP) O… | — | Subarachnoid Hemorrhage | Terminated | 2009-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00927940 | RESOLUTE Japan - The Clinical Evaluation of the MDT-4107 Drug-Eluting Coronary … | Na | Arterial Occlusive Diseases | Completed | 2009-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00847288 | OptiVol® Care Pathway | Phase4 | Heart Failure | Completed | 2009-03-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00863213 | Study of Ablation Versus antiaRrhythmic Drugs in Persistent Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01400659 | Pizza-Salami Study in Children and Adolescents With Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2009-03-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00880230 | Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE) | Na | Peripheral Artery Disease | Completed | 2009-03-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00841529 | Evaluation of the Cardioblate Closure Device in Facilitating Occlusion of the L… | Phase2 | Left Atrial Appendage Occlusion | Terminated | 2009-03-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00853593 | Model 4396 Left Ventricular (LV) Lead Study | Na | Heart Failure | Completed | 2009-03-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00865345 | An Inpatient Evaluation of Six-Day Subcutaneous Glucose Sensor Performance | Na | Diabetes | Completed | 2009-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00889681 | Continued Access Protocol | Na | Atrial Fibrillation | Completed | 2009-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00869921 | Model 4195 Left Ventricular (LV) Lead Chronic Performance Study | — | Heart Failure | Completed | 2009-03-01 | 2018-04-03 | ClinicalTrials.gov |
| NCT00866502 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Parkinson's Disease | Completed | 2009-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01338493 | Maverick Total Disc Replacement in a 'Real World' Patient Population | — | Degenerative Disc Disease | Completed | 2009-02-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00839384 | AdvisaTM IPG Clinical Evaluation Study | Na | Bradycardia | Completed | 2009-02-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00850213 | Assessment of Clinical Performance and Costs of the Endeavor Resolute Stent "in… | — | Coronary Artery Disease | Completed | 2009-02-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT04905303 | Solitaire Aneurysm Remodeling Registry | — | Intracranial Saccular Aneurysm, Either Rupture or Unruptured | Withdrawn | 2009-02-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01085513 | Diagnosis of Intestinal Motility by Image Analysis Using Capsule Endoscopy | Na | Intestinal Abnormalities | Terminated | 2009-02-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00837486 | Reclaim Deep Brain Stimulation Clinical Study for Treatment-Resistant Depression | Phase2 | Depression | Completed | 2009-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00790088 | INTERPRET - International Report on Routine Practice of Sensor-enabled Pump The… | — | Diabetes Mellitus, Type 1 | Completed | 2009-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00843401 | Clinical Performance Evaluation of Pediatric and Neonatal Low Saturation Oximet… | — | Low Oxygen Saturation | Completed | 2009-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00772421 | Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy - Recruitment … | — | Epilepsy | Completed | 2009-01-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00827411 | Double Randomization of a Monitoring Adjusted Antiplatelet Treatment Versus a C… | Phase4 | Coronary Artery Disease | Completed | 2009-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00846846 | PROTECT Continued Access Post Marketing Surveillance Trial | Phase4 | Coronary Artery Disease, Autosomal Dominant, 1 | Completed | 2009-01-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01347554 | Efficacy of Everolimus-Eluting Versus Zotarolimus-Eluting Sten for Coronary Les… | Phase4 | Myocardial Infarction | Completed | 2009-01-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00960908 | Registry to Evaluate the Efficacy of Zotarolimus-Eluting Stent | — | Coronary Artery Disease | Unknown | 2009-01-01 | — | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00798174 | The Effect of an Azygos Vein Coil on Defibrillation Threshold | Na | Heart Failure | Completed | 2008-12-15 | 2009-11-18 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00943150 | PEAK PlasmaBlade™ vs. Traditional Electrosurgery in Abdominoplasty | Na | Elastosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00789542 | A RCT to Establish the Effectiveness of Intermittent Pneumatic Compression to P… | Phase3 | Stroke | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00894062 | Comparison of Neointimal Coverage Between Zotarolimus Eluting Stent and Everoli… | Phase4 | Coronary Artery Disease | Completed | 2008-12-01 | — | ClinicalTrials.gov |
| NCT00800501 | A Safety and Tolerability Study of Intracerebroventricular Administration of sN… | Phase1 | Amyotrophic Lateral Sclerosis | Completed | 2008-12-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00816062 | Post-Approval Trial of the Talent™ Abdominal Stent Graft to Treat Aortic Aneury… | Na | Aortic Aneurysm, Abdominal | Completed | 2008-12-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829621 | Incisional Vacuum Assisted Closure (IVAC) Device and Its Effect on Implanted Bo… | Na | Fractures, Closed | Completed | 2008-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00822146 | Cardiac Resynchronization Therapy (CRT) Efficacy Study | Na | Heart Failure | Completed | 2008-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00787800 | The Use of Dual Chamber ICD With Special Programmed Features to Lower the Risk … | Phase4 | Ventricular Tachycardia | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00800657 | Stem Cells and Resynchronization Cardiac | Phase1 | Heart Failure | Unknown | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00821938 | Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study | Phase4 | Heart Failure | Completed | 2008-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT00839566 | PAF-HEFT (Permanent Atrial Fibrillation in Heart Failure Trial) | Phase4 | Atrial Fibrillation | Terminated | 2008-11-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00875290 | The Effectiveness of Continuous Glucose Monitoring in Diabetes Treatment for In… | Phase3 | Diabetes Mellitus, Type I | Unknown | 2008-11-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01185392 | European Cardiac Resynchronisation Therapy Survey | — | Heart Failure | Completed | 2008-11-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00790725 | Proportional Assist Ventilation vs Pressure Support Ventilation | Na | Respiration, Artificial | Terminated | 2008-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00749268 | AbsorbaTack Evaluation of Postoperative Pain Following Laparoscopic Hernia Repa… | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01434615 | Medtronic South Asian Systolic Heart Failure Registry | Phase4 | Heart Failure | Completed | 2008-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00827944 | Parietex Progrip Study | Phase4 | Hernia, Inguinal | Completed | 2008-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00753337 | The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of … | Na | Peripheral Vascular Disease | Completed | 2008-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00885235 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Bowel Diseases | Completed | 2008-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01018667 | Assessment of Efficacies of Cardiac Resynchronization Therapies (CRT-P/D) for H… | — | Heart Failure | Unknown | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00753116 | Renal Denervation in End Stage Renal Disease Patients With Refractory Hypertens… | Phase1 | Kidney Failure, Chronic | Completed | 2008-09-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00769457 | OptiLink HF Study: Optimization of Heart Failure Management Using Medtronic Opt… | Phase4 | Heart Failure | Completed | 2008-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00731172 | A Double Blind Placebo Control Study to Assess the Safety,Tolerability and Effi… | Phase2 | Crohns Disease | Unknown | 2008-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00745706 | Discerning Symptomatic and Asymptomatic Episodes Pre and Post Radiofrequency Ab… | Na | Atrial Fibrillation | Completed | 2008-09-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00752128 | RESOLUTE International Registry: Evaluation of the Resolute Zotarolimus-Eluting… | — | Coronary Artery Disease | Completed | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00775346 | A Multi-Center Study to Assess the Performance of Saturation Patterns. | — | Sleep-Disordered Breathing | Completed | 2008-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00656708 | Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associate… | Na | Burns | Completed | 2008-08-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00737581 | Spinal Cord Stimulation Research Study | — | Chronic Low Back and Leg Pain | Completed | 2008-08-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00669552 | Intracardiac T-wave Alternans and Ischemia | — | Ischemia | Completed | 2008-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01213615 | Hancock II Ultra Porcine Bioprosthesis Hemodynamic Study | — | Aortic Heart Valve Diseases | Completed | 2008-08-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01015612 | CoreValve® System Australia/New Zealand Clinical Study | Na | Aortic Valve Stenosis | Completed | 2008-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00669682 | T-wave Alternans and Intrathoracic Impedance Measurements | — | Congestive Heart Failure | Completed | 2008-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00824915 | Enhanced Surveillance of RV Lead Integrity Alert (RVLIA) | — | Shock | Completed | 2008-08-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01060449 | Stimulus Intensity in Left Ventricular Leads | Na | Congestive Heart Failure | Completed | 2008-08-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00915720 | Implanted Loop Recorder Post Atrial Fibrillation Ablation | — | Atrial Fibrillation | Unknown | 2008-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00845234 | Establishing a Standard for Peri-operative Implantable Cardioverter Defibrillat… | Na | Arrhythmia | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01103492 | Treatment of Hemorrhagic Radiation Proctitis Using the Halo System | Na | Pelvic Neoplasms | Completed | 2008-07-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01076374 | MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY | — | Arrhythmia | Completed | 2008-07-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00949208 | Development of Applications of the Given® Diagnostic System and Evaluation of T… | — | Healthy | Completed | 2008-07-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT00703794 | Researching AXIUM Coiling Experience and Recanalization (RACER) | — | Aneurysms | Completed | 2008-06-01 | 2012-01-16 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT01051310 | Medtronic CoreValve REDO Study | Na | Aortic Valve Stenosis | Completed | 2008-06-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00705718 | Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System | Na | Abdominal Aortic Aneurysms | Completed | 2008-06-01 | 2016-09-26 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00707434 | Continuous Glucose Monitoring in Critically Ill | Na | Diabetes | Terminated | 2008-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00736424 | Brain Stimulation for Epilepsy Long Term Follow-up | — | Epilepsy | Completed | 2008-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00734409 | Combining Objective and Subjective Sedation Assessment Tools | Na | Critical Illness | Completed | 2008-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00850291 | Economisation of Whipple Resection Using Electrosurgical Sealing Device | — | Duodenopancreatectomy | Completed | 2008-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00873899 | Evolution of Management Strategies of Heart Failure Patients With Implantable D… | — | Heart Failure | Unknown | 2008-05-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01133925 | Optical Coherence Tomography in Long Lesions | Phase4 | Coronary Artery Disease | Unknown | 2008-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00689130 | ADVANCE: Assessment for Defining Variability in Anesthesia Through Novel Clinic… | — | Pain | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00875810 | PRESTIGE Observational Study | — | Degenerative Cervical Disc Disease | Completed | 2008-04-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00617084 | Randomized, Two-arm, Non-inferiority Study Comparing Endeavor-Resolute Stent Wi… | Phase4 | Coronary Artery Disease | Completed | 2008-04-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT00664638 | Renal Denervation in Patients With Refractory Hypertension | Na | Hypertension | Completed | 2008-04-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00680550 | INSIGHT (R)XT. Indications for Diagnosis, Arrhythmia and Monitoring of Reveal XT | — | Atrial Fibrillation | Completed | 2008-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00664807 | Medtronic Genetic Arrhythmia Markers for Early Detection (GAME Study) | — | Death, Sudden, Cardiac | Completed | 2008-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00729781 | Study of Polyester Implants for the Treatment of External Nasal Valve Collapse … | Phase1 | Nasal Alar Collapse, Bilateral | Terminated | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00704561 | Vessel Wall Response of the Zotarolimus Drug-eluting Stent Implanted in AMI Ass… | Na | Acute Myocardial Infarction | Completed | 2008-04-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00658983 | Autologous Platelet Enriched Gel Versus Metalloproteinase Inhibitor in the Heal… | Na | Chronic Lower Leg Ulcer | Completed | 2008-04-01 | 2010-08-20 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00631709 | REmote MOnitoring Transmission Evaluation of IPGs | Phase4 | Pacemaker | Completed | 2008-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01026935 | The Outcome After Lichtenstein Operation vs. ProGrip Patch Repair of Inguinal H… | Na | Inguinal Hernia | Completed | 2008-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00627497 | DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolatera… | Phase3 | Degenerative Lumbar Spinal Stenosis | Terminated | 2008-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00885339 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Preparation and Proce… | — | Colonic Diseases | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00753753 | VerifyNow French Registry | — | Stent Thrombosis | Completed | 2008-02-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00641251 | DSS: Diabetes Surgery Study - Intensive Medical Management of Type 2 Diabetes, … | Na | Type 2 Diabetes | Completed | 2008-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00596973 | Surgical Treatment of Type 2 Diabetes in Non-Morbidly Obese Patients | Phase4 | Diabetes | Withdrawn | 2008-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00609947 | Endeavor Zotarolimus - Eluting Stent in the Treatment Lesions in Small Native C… | Na | Coronary Artery Disease | Completed | 2008-01-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00598663 | SWITCH - Sensing With Insulin Pump Therapy to Control HbA1c | Na | Diabetes Mellitus, Type 1 | Completed | 2008-01-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00885469 | PillCam® ESO 2 in Esophageal Pathologies | — | Barrett's Esophagus | Completed | 2007-12-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00589303 | AV Node Ablation and Pacemaker Therapy Compared to Drug Therapy for Atrial Fibr… | Phase3 | Atrial Fibrillation | Terminated | 2007-12-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00637260 | Motor Cortex Stimulation for Parkinson's Disease | Na | Parkinson's Disease | Completed | 2007-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00854048 | The Performance of Pulse Oximeters in Pediatric Patients With Low Oxygen Satura… | — | Cardiopulmonary Bypass | Completed | 2007-12-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00793312 | China Endeavor Registry: A Registry With The Endeavor Zotarolimus Eluting Coron… | — | Coronary Artery Disease | Completed | 2007-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00559143 | Biventricular Alternative Pacing | Phase4 | Atrioventricular Block | Withdrawn | 2007-11-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00730730 | The Complete® Self-Expanding Stent and Stent Delivery System Registry | Na | Peripheral Vascular Disease | Completed | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00730041 | Palatal Implants in Combination With Continuous Positive Airway Pressure to Tre… | Phase4 | Obstructive Sleep Apnea (OSA) | Terminated | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00558129 | Effects of X-STOP® Versus Laminectomy Study | Phase4 | Lumbar Spinal Stenosis | Withdrawn | 2007-11-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01803217 | Evaluation of Pacemaker Algorithms to Avoid Unnecessary Right Ventricular Pacing | Na | Pacemaker Implantation for Sinus Node Disease | Completed | 2007-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT00730548 | Compare Remote Patient Management and Standard Care in CRT-D and ICD-patients t… | Na | Heart Failure | Completed | 2007-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00688571 | Melody Transcatheter Pulmonary Valve (TPV) Post-Market Surveillance Study | Na | Heart Valve Diseases | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00547378 | InSite for Over Active Bladder | Phase4 | Urinary Incontinence, Urgency-frequency | Completed | 2007-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00565617 | Epidural Cortical Stimulation for Depression | Na | Treatment Resistant Depression | Active_Not_Recruiting | 2007-10-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526162 | ConsultaTM CRT-D Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00744874 | Ablation of the Pulmonary Veins for Paroxysmal Afib | Phase4 | Paroxysmal Atrial Fibrillation | Completed | 2007-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00551304 | Native Kidney Denervation in Patients With End Stage Renal Disease | Phase1 | End Stage Renal Disease | Completed | 2007-10-01 | — | ClinicalTrials.gov |
| NCT01089634 | Left Ventricular Capture Management Study | — | Ventricular Fibrillation | Completed | 2007-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00510198 | Evaluation of Cardiac Compass With OptiVol in the Early Detection of Decompensa… | Na | Congestive Heart Failure | Terminated | 2007-10-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00526227 | SecuraTM ICD Clinical Evaluation Study | Na | Tachyarrhythmias | Completed | 2007-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT02685280 | Rechargeable Neurostimulators in Deep Brain Stimulation for Psychiatric Disorde… | Na | Obsessive-compulsive Disorder | Completed | 2007-10-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00505323 | Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia… | Phase1 | Focal Dystonia | Completed | 2007-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00506493 | Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CU… | Phase3 | Atrial Fibrillation | Completed | 2007-09-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00507559 | The Pivotal Study of the Aptus Endovascular AAA Repair System | Na | Abdominal Aortic Aneurysms (AAA) | Completed | 2007-09-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00846001 | Resynchronization Surgery Combined Unified Efficacy | Phase3 | Ischemic Heart Failure | Completed | 2007-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00487396 | Evaluation of Capsule Endoscopy in Patients With Suspected Crohn's Disease | Na | Crohn's Disease | Completed | 2007-09-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00680927 | Reveal® XT Performance Trial (XPECT) | Phase4 | Atrial Fibrillation | Completed | 2007-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00517751 | Condition of Approval Study | Phase4 | Lumbar Spinal Stenosis | Terminated | 2007-08-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00461734 | PROTECT-PACE STUDY - The Protection of Left Ventricular Function During Right V… | Na | Left Ventricular Dysfunction | Completed | 2007-08-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT00530712 | Safety and Effectiveness Study of EverFlex Stent to Treat Symptomatic Femoral-p… | Na | Peripheral Vascular Diseases | Completed | 2007-08-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00848237 | HALO Patient Registry: Ablation of Barrett's Esophagus | Na | Barrett Esophagus | Completed | 2007-07-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00488501 | Clinical Usefulness and Efficacy of Intrathoracic Impedance Monitoring Using th… | — | Heart Failure | Completed | 2007-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00469482 | The SOMNUS Study: Sedative Optimization Via Monitoring Neurological Status | Na | Delirium | Completed | 2007-06-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00485173 | INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clin… | Na | Degenerative Disc Disease | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00431457 | Controlled Randomized Stimulation Versus Resection (CoRaStiR) | Na | Epilepsy | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00476957 | Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) | Phase4 | Ischemic Heart Disease | Completed | 2007-06-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00464529 | Accuracy and Safety of Real Time Continuous Glucose Monitoring Before, During a… | — | Glucose Metabolism Disorders | Completed | 2007-05-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00444067 | Study to Evaluate Safety & Effectiveness of Spinal Sealant | Na | Cerebrospinal Fluid Leakage, Subdural | Completed | 2007-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00530504 | Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval … | Na | Carotid Artery Disease | Completed | 2007-05-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00431834 | Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE… | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00514735 | Tailored Treatment of Permanent Atrial Fibrillation | Phase3 | Atrial Fibrillation | Completed | 2007-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00590473 | Sacral Neuromodulation in Patients With IC | Na | Interstitial Cystitis | Completed | 2007-04-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00456352 | Duodenal Exclusion for the Treatment of T2DM | Phase4 | Diabetes | Completed | 2007-04-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00604422 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in Detection & Classi… | — | Colonic Disease | Completed | 2007-04-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00509392 | ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter,… | Phase4 | Venous Reflux | Completed | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00480077 | Diagnostic Outcome Trial in Heart Failure (DOT-HF Trial) | Phase4 | Heart Failure | Terminated | 2007-03-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00618358 | Vascular Sealant Study | Phase1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | Terminated | 2007-03-01 | — | ClinicalTrials.gov |
| NCT00443781 | Study Of Disc Anaesthesia For The Preoperative Diagnosis Of Chronic Lower Back … | Phase4 | Low Back Pain | Completed | 2007-03-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00433654 | EMRI SureScan™ Clinical Study | Na | Bradycardia | Completed | 2007-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00478933 | DISCOVERY: Diagnostic Data and Genetic Polymorphisms in ICD Patients. | Na | Death, Sudden, Cardiac | Completed | 2007-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00370526 | HEAL-HF: A Cardiac Resynchronization Therapy (CRT) Outcomes Study | Phase4 | Heart Failure, Congestive | Terminated | 2007-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00603213 | Correlation of Intrathoracic Impedance Measures With Blood Plasma Volume in Con… | — | Congestive Heart Failure | Completed | 2007-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00433043 | BOAT: Beta Blocker Uptitration With OptiVol After Cardiac Resynchronization The… | Phase4 | Congestive Heart Failure | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00845624 | Time Outside Target Oxygen Saturation Range in Preterm Infants and Long Term Ou… | — | Retinopathy of Prematurity | Completed | 2007-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00417989 | Study to Compare Efficacy of the MiniMed Paradigm REAL-Time System Vs. MDI in S… | Na | Type 1 Diabetes | Completed | 2007-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00422669 | Optimize RV Selective Site Pacing Clinical Trial | Na | Cardiac Pacing, Artificial | Terminated | 2007-01-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT01389089 | Effective Treatment of Posttraumatic and Postoperative Edema | Na | Edema | Completed | 2007-01-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00401882 | Treatment of Ventricular Tachyarrhythmias Refractory To Shock With Beta Blocker… | Phase2 | Cardiac Arrest | Terminated | 2007-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00209053 | SMART Trial Longitudinal Follow-Up:Off-Pump Versus On-Pump Coronary Artery Bypa… | Na | Coronary Artery Disease | Completed | 2007-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00740870 | Melody Transcatheter Pulmonary Valve Study: Post Approval Study of the Investig… | Na | Congenital Heart Defects | Completed | 2007-01-01 | 2020-08-21 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00606567 | A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillat… | Na | Tachycardia, Ventricular | Completed | 2006-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00420108 | Optivol Diagnostic Data for Discharge in Heart Failure | — | Heart Failure, Congestive | Completed | 2006-12-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00413231 | Valor II: The Valiant Thoracic Stent Graft System Clinical Study | Na | Thoracic Aortic Aneurysm | Completed | 2006-12-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01213589 | The VIRTUE Post Marketing Surveillance Registry | — | Aortic Dissection | Completed | 2006-12-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00621621 | CryoCath Freezor CryoAblation Catheter System (CRYOFACTS) | Phase4 | Tachycardia, Atrioventricular Nodal Reentry | Completed | 2006-12-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00456378 | Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Vers… | Na | Lumbar Degenerative Disc Disease | Terminated | 2006-12-01 | 2018-11-20 | ClinicalTrials.gov |
| NCT00414466 | A Safety and Effectiveness Study of Intraspinal Gabapentin (MDT2004) for the Tr… | Phase2 | Chronic Intractable Pain | Terminated | 2006-12-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00954421 | Use of Two Deep Brain Stimulation (DBS) Electrodes to Treat Post-Traumatic Trem… | Na | Multiple Sclerosis | Completed | 2006-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00749996 | Herniectomy Versus Herniectomy With a Spinal Stabilization System for the Treat… | Phase4 | Sciatica | Completed | 2006-11-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00538369 | Combining Observational and Physiologic Sedation Assessment Tools | Phase4 | Brain Injury | Terminated | 2006-11-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT01169441 | Lead Extract Study | — | Cardiac Surgical Procedures | Completed | 2006-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00402246 | CONNECT Study - Clinical Evaluation Of Remote NotificatioN to rEduCe Time to Cl… | Na | Arrhythmia | Completed | 2006-11-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00887744 | Intermittent Neurogenic Claudication Treatment With APERIUS® | Phase4 | Spinal Stenosis | Completed | 2006-11-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00523978 | A Clinical Study of the Arctic Front Cryoablation Balloon for the Treatment of … | Phase3 | Paroxysmal Atrial Fibrillation | Completed | 2006-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00385749 | Right Ventricular Defibrillation Lead Select Site Study | Na | Heart Failure, Congestive | Unknown | 2006-10-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00418067 | Zotarolimus-Eluting Stent Versus Sirolimus-Eluting Stent and PacliTaxel-Eluting… | Phase4 | Coronary Artery Disease | Completed | 2006-10-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00604162 | PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization of the Colon | Phase3 | Colonic Diseases | Completed | 2006-10-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00372138 | Prevention of Endoleaks Using Autologous Platelet Gel on Unruptured Abdominal A… | Na | Abdominal Aortic Aneurysms | Terminated | 2006-09-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00318357 | CARE-HF Long Term Follow-up | — | Heart Failure | Completed | 2006-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00359203 | ISSUE3: International Study on Syncope of Uncertain Etiology 3 | Phase4 | Syncope | Completed | 2006-09-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00637754 | Safety of Sports for Patients With Implantable Cardioverter-Defibrillators | — | Heart Arrhythmias | Completed | 2006-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00418860 | The Optimal Duration of Dual Antiplatelet Therapy After Implantation of Endeavo… | Na | Coronary Artery Disease | Completed | 2006-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01290952 | On Versus Off Pump Myocardial Revascularization Study | Phase4 | Coronary Artery Disease | Completed | 2006-09-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00376532 | Extracellular Matrix Marker of Arrhythmia Risk (EMMA) | — | Myocardiopathies | Completed | 2006-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00744835 | Atrial Fibrillation Ablation Pilot Study | Phase1 | Atrial Fibrillation | Completed | 2006-08-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00323609 | KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restorati… | Na | Vertebral Body Compression Fractures | Terminated | 2006-08-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00693030 | Optical Coherence Tomography for Drug Eluting Stent Safety | Phase4 | Coronary Artery Disease | Unknown | 2006-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00338715 | Effectiveness of Pulmonary Vein Isolation in Prevention of Atrial Fibrillation … | Phase3 | Atrial Fibrillation | Completed | 2006-07-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00440791 | Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) in the Visualization … | — | Colonic Diseases | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00504647 | Biventricular Pacing in Hypertrophic Cardiomyopathy | Phase1 | Hypertrophic Cardiomyopathy | Unknown | 2006-06-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00328705 | D2-EPG Study: Evaluation of New Sensing Circuitry and Capture Management | Na | Heart Diseases | Completed | 2006-05-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00351208 | Spinal Cord Stimulation Efficacy Measures | Phase1 | Chronic Pain in the Trunk and Limbs | Unknown | 2006-05-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01388907 | Efficacity Assessment of PREVADH® in Adhesion Prevention in Gynaecologic Surgery | Phase4 | Uterine Fibroids | Completed | 2006-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01051518 | Clinical Evaluation of Percutaneous Implantation of the Medtronic CoreValve Aor… | Na | Aortic Valve Stenosis | Completed | 2006-05-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01116024 | ATS 3f Enable(tm) Aortic Bioprosthesis, Model 6000 | Na | Heart Valve Diseases | Completed | 2006-05-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00331669 | Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Pa… | Phase2 | Dystonia | Unknown | 2006-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00477555 | Hemodynamic Assessment of Mosaic Ultra Stented Heart Valve in the Aortic Positi… | — | Aortic Valve Replacement | Completed | 2006-04-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00842296 | ClosureFAST - Radiofrequency Great Saphenous Vein Treatment | Na | Venous Reflux | Completed | 2006-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01067885 | A Post-market Registry of the MARIS-stent (Invatec) Implanted in the Superficia… | Na | Peripheral Artery Disease | Completed | 2006-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00354159 | Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients Wit… | Na | Heart Failure | Completed | 2006-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00450710 | Neuroendocrine Brake for Type 2 Diabetes Mellitus | Phase4 | Diabetes | Completed | 2006-03-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00288288 | Prospective Registry of Epicardial LV Leads Placed During Cardiac Surgery Proce… | — | Chronic Heart Failure | Completed | 2006-03-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00286962 | Study to Compare Intraperitoneal Insulin to Subcutaneous Insulin Administration… | Phase3 | Diabetes Mellitus, Type 1 | Completed | 2006-02-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00262119 | MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and H… | Phase4 | Atrial Fibrillation | Completed | 2006-02-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00530023 | Feasibility Study for Training Pump Naïve Subjects To Use The Paradigm® System … | Phase4 | Type 1 Diabetes | Completed | 2006-02-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00293943 | Randomized Trial of Two Different Strategies to Treat Paroxysmal Atrial Fibrill… | Na | Atrial Fibrillation | Completed | 2006-02-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00282672 | Ablation of Intestinal Metaplasia Containing Dysplasia | Na | Barrett Esophagus | Completed | 2006-02-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00293241 | PreFER Managed Ventricular Pacing (MVP) For Elective Replacement | Phase4 | Cardiovascular Diseases | Completed | 2006-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00308984 | CARE--Childhood Awareness and Recall Evaluation | — | Anesthesia | Completed | 2006-01-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00289523 | EEG Biomarkers for Predicting Response to Antidepressant Therapy | — | Major Depressive Disorder | Completed | 2006-01-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00316446 | Study to Determine Incidence of Hypoventilation in Patients Who Have Undergone … | — | Morbid Obesity | Completed | 2006-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00314275 | The ENDEAVOR Pharmacokinetic (PK) Registry: The Medtronic Endeavor Drug Eluting… | Na | Coronary Artery Disease | Completed | 2006-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00246805 | Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post M… | Phase4 | Permanent Atrial Fibrillation | Completed | 2006-01-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00239226 | Electrophysiologically Guided PAcing Site Selection Study | Phase4 | Sinus Arrhythmia | Completed | 2005-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00307957 | Study to Determine the Effectiveness of Pillar Palatal Implants to Treat Obstru… | Phase4 | Obstructive Sleep Apnea | Completed | 2005-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00240149 | Pilot Study to Evaluate a Method of Controlling High Blood Sugar in the Pediatr… | Na | Hyperglycemia | Completed | 2005-10-01 | 2006-03-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00704340 | DuraSeal Sealant Post Market Study | Na | Elective Cranial Procedures With Dural Incision | Completed | 2005-09-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00179972 | Evaluation of Pulse Oximetry Sensors in Neonates | — | Premature Birth | Terminated | 2005-09-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00157807 | Clinical and Economic Consequences of Left Atrial Bipolar Radiofrequency Ablati… | Na | Atrial Fibrillation | Terminated | 2005-09-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00139542 | AED Use in Out-of-Hospital Cardiac Arrest: A New Algorithm Named "One Shock Per… | Phase3 | Heart Arrest | Completed | 2005-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00560339 | Does Lung Impedance Correlate With Changes in BNP in Stable and Acutely Decompe… | — | Congestive Heart Failure | Unknown | 2005-09-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00234611 | Localization of CRT According to Echocardiography: LOCATE-Pilot Study | Na | Heart Failure | Unknown | 2005-09-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00277524 | OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Card… | — | Tachycardia, Ventricular | Terminated | 2005-08-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00432835 | Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis | Phase3 | Gastroparesis | Completed | 2005-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00251823 | Safety and Efficacy Study of Eptifibatide in Primary Percutaneous Coronary Inte… | Phase3 | Myocardial Infarction | Completed | 2005-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00122031 | Deep Brain Stimulation for Treatment-Refractory Major Depression | Phase1 | Depression | Completed | 2005-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01491568 | rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) | Na | Degenerative Disc Disease | Completed | 2005-07-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00125086 | Platelets for Acute Wound Healing | Na | Wounds | Completed | 2005-07-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00148889 | Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal St… | Phase3 | Cervical Dystonia | Completed | 2005-07-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00148369 | A Multi-Center, Observational Safety Registry of Subjects With Idiopathic Parki… | — | Idiopathic Parkinson's Disease | Completed | 2005-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00211510 | Use of the Paradigm 722 System to Improve Glycemic Control in Adult and Adolesc… | Na | Type 1 Diabetes | Completed | 2005-06-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00200018 | Study of Weight Loss Using Gastric Stimulation in Obese Patients With Type 2 Di… | Na | Severe to Morbid Obesity and Type 2 Diabetes | Completed | 2005-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00311909 | Thalamic Deep Brain Stimulation for Tourette Syndrome | Phase2 | Tourette Syndrome | Completed | 2005-06-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00122915 | CONCEPT: Crossover Efficacy Pain Trial in Motor Cortex Stimulation for Intracta… | Phase3 | Pain, Intractable | Terminated | 2005-06-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00307073 | Adapta Pacing System Clinical Study | Na | Pacemaker | Completed | 2005-05-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00211237 | CAFE Study - Cancer Patient Fracture Evaluation | Na | Cancer | Completed | 2005-05-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00111527 | APAF: Assessment of Cardiac Resynchronization Therapy in Patients With Permanen… | Phase3 | Congestive Heart Failure | Completed | 2005-05-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00303979 | IMPROVE HF: Registry to Improve the Use of Evidence-Based Heart Failure Therapi… | — | Heart Failure, Congestive | Completed | 2005-05-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00217269 | The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary … | Na | Coronary Artery Disease | Completed | 2005-04-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00153257 | Comparative Study of Mesh Versus No Mesh in Prolapse Surgery | Na | Vaginal Prolapse | Completed | 2005-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00199498 | Right Apical Versus Septal Pacing Trial | Na | Heart Block | Unknown | 2005-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00773851 | Transfacial Sutures Versus Stapler for Mesh Fixation in Laparoscopic Ventral He… | Na | Ventral Hernia | Completed | 2005-04-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00310947 | Impact of Patient-Prosthesis-Mismatch on Coronary Flow Reserve | — | Coronary Artery Disease | Completed | 2005-03-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00223132 | Suture Granuloma in Body Contouring Surgery | Phase4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | Completed | 2005-02-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00667459 | Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cerv… | Phase3 | Cervical Degenerative Disc Disease | Completed | 2005-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT00400985 | Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Fa… | Na | Heart Failure, Congestive | Completed | 2005-01-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00215761 | Recurrence of Atrial Fibrillation in Patients With Dual-chamber Pacemakers and … | — | Atrial Fibrillation | Completed | 2005-01-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00200122 | Restore Claims Characterization Study | Phase4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | Completed | 2005-01-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00199992 | Platelets in Acute Wounds: A Pilot Study (PAWS) | Na | Wounds | Completed | 2005-01-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT01921543 | Deep Brain Stimulation in Treatment Refractory Depression | Phase1 | Major Depressive Disorder | Terminated | 2005-01-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00161551 | Mode Evaluation in Sick Sinus Syndrome Trial (MODEST) | Phase4 | Sick Sinus Syndrome | Unknown | 2004-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00773019 | SynchroMed II Post-Approval Study | — | Severe Spasticity | Completed | 2004-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00303641 | Safety and Effectiveness of the Medtronic Resting Heart Bypass System in Heart … | Phase1 | Coronary Artery Bypass Surgery | Completed | 2004-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00429611 | High Low Biphasic Energy Defibrillation (HiLoBED) | Phase3 | Ventricular Fibrillation | Unknown | 2004-11-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00111228 | The Guardcontrol Trial: Study to Assess if Type 1 Diabetics Can Improve Using t… | Na | Diabetes Mellitus | Completed | 2004-10-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00281099 | Managed Ventricular Pacing ("MVP") Trial | Na | Heart Disease | Terminated | 2004-10-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00095095 | Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™… | Phase4 | Low Back Pain | Terminated | 2004-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00271154 | REsynchronization reVErses Remodeling in Systolic Left vEntricular Dysfunction … | Na | Heart Failure | Completed | 2004-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT01690260 | Parallel Study Between BMP-2 and Autologous Bone Graft After Ilizarow Treatment | Phase1 | Bone Degenerative Changes | Completed | 2004-09-01 | 2017-10-02 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00269230 | Attain StarFix™ Model 4195 Left Ventricular Lead | Na | Heart Failure | Completed | 2004-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT01331343 | Effectiveness Study of the Guardian RT in Type 1 Diabetics | Phase4 | Type 1 Diabetes Mellitus | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00279955 | PARTNERS HF: Program to Access and Review Trending Information and Evaluate Cor… | — | Heart Failure, Congestive | Completed | 2004-06-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00200109 | Occipital Nerve Stimulation for the Treatment of Chronic Migraine Headache. | Phase1 | Chronic Migraine Headache | Completed | 2004-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00182416 | Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial | Phase3 | Pacemaker Dependence | Completed | 2004-05-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00291564 | Ensure Cardiac Resynchronization Therapy Study | — | Heart Failure | Completed | 2004-05-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00273195 | Clinical Investigation of the Medtronic EnTrust™ Implantable Cardioverter Defib… | Na | Ventricular Arrhythmias | Completed | 2004-04-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00147264 | Telmisartan-Induced Reduction in Intra-Myocellular Lipids Trial | Phase3 | Metabolic Syndrome X | Completed | 2004-04-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00064649 | Minimally Invasive Surgical Therapy for BPH | Phase3 | Benign Prostatic Hyperplasia | Terminated | 2004-04-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00294645 | PREFER (Pacemaker Remote Follow-Up Evaluation and Review) | Na | Bradycardia | Completed | 2004-04-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00619775 | Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial | Phase3 | Carotid Artery Disease | Completed | 2004-04-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00253357 | PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy | — | Heart Failure | Completed | 2004-03-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00275769 | CAPTURE - Complete Automatic Pacing Threshold Utilization Recorded by EnPulse | Na | Arrhythmia | Completed | 2004-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00294060 | P3: Pacemaker Patient Profiling Study | — | Bradycardia | Terminated | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147277 | ADVANCE-D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable Cardi… | Phase4 | Tachycardia, Ventricular | Completed | 2004-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00147290 | ADVANCE CRT - D: Antitachycardia Pacing (ATP) Delivery for Painless Implantable… | Phase4 | Tachycardia, Ventricular | Completed | 2004-02-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00217256 | The Medtronic Endeavor III Drug Eluting Coronary Stent System Clinical Trial | Na | Coronary Artery Disease | Completed | 2004-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00157794 | EnTRINSIC - EnPulse Trial on Search AV+ Influence | Phase4 | Arrhythmia, Sinus | Terminated | 2004-02-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00279968 | INSIGHTS ICD Registry | — | Ventricular Tachycardia | Completed | 2004-02-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT01007474 | One Hospital ClinicalService Project | — | Arrhythmias, Cardiac | Withdrawn | 2004-01-01 | 2030-01-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00555698 | Feasibility, Safety and Efficacy of Deep Brain Stimulation for Depression | Early_Phase1 | Depression | Completed | 2004-01-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00270933 | MAVRIC VR ICD Registry | — | Ventricular Tachycardia | Completed | 2004-01-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00223119 | Comparison of Absorbable Sutures in Perineal Laceration Repair | Phase4 | Perineal Laceration Repair | Terminated | 2004-01-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00170313 | CORE: Study to Evaluate the Conducted AF-Response-Algorithm in Patients Sufferi… | Phase4 | Heart Failure | Terminated | 2003-12-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00101933 | SANTE - Stimulation of the Anterior Nucleus of the Thalamus for Epilepsy | Phase3 | Epilepsy | Completed | 2003-12-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00111982 | Trial of Extended Treatment With Liatermin (r-metHuGDNF) Administered by Contin… | Phase1 | Parkinson's Disease | Completed | 2003-12-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00267098 | Biventricular Versus Right Ventricular Pacing in Heart Failure Patients With At… | Na | Atrioventricular Block | Completed | 2003-12-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00279981 | TRENDS: A Prospective Study of the Clinical Significance of Atrial Arrhythmias … | — | Atrial Fibrillation | Completed | 2003-11-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00555737 | Performance Evaluation of Capsule Endoscopy in the Diagnosis of Gluten Sensitiv… | — | Celiac Disease | Completed | 2003-11-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00289276 | FAST (Fluid Accumulation Status Trial) | Na | Congestive Heart Failure | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00157846 | X-Change HF - Exchange of the Existing Pacemaker/ICD in Bradycardia Patients Su… | Phase4 | Heart Failure, Congestive | Terminated | 2003-10-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00305240 | MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post M… | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00305214 | MASTER II - Microvolt T Wave Alternans Testing for Risk Stratification of Post … | Na | Myocardial Infarction | Completed | 2003-10-01 | 2007-02-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00156728 | Study to Characterize Atrial Fibrillation in CHF Patients Indicated for CRT | Phase4 | Congestive Heart Failure, Atrial Fibrillation | Completed | 2003-10-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00279279 | PREPARE - Primary Prevention Parameters Evaluation | Na | Tachycardia, Ventricular | Completed | 2003-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT01570257 | A Trial of High and Low Pressure Level Settings on a Programmable Ventriculoper… | Na | Idiopathic Normal Pressure Hydrocephalus | Completed | 2003-09-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00661232 | Multicenter Myocardial Viability Trial | — | Coronary Artery Disease | Completed | 2003-08-11 | 2011-05-15 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00959296 | Implantable Systems Performance Registry | — | Spinal Cord Stimulation | Completed | 2003-08-01 | 2016-09-27 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604799 | VALOR: The Talent Thoracic Stent Graft System Clinical Study | Phase2 | Thoracic Aortic Aneurysms | Completed | 2003-07-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01491516 | TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study | Na | Degenerative Disc Disease | Completed | 2003-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00604552 | AneuRx Post Market Study in the Treatment of AAA | Na | Abdominal Aneurysm | Terminated | 2003-07-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00437190 | Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of … | Na | Radiculopathy | Completed | 2003-06-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00268294 | Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial F… | Na | Heart Failure, Atrial Arrhythmia | Completed | 2003-05-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00360984 | Prevention of Severe Hypoglycemia in Type 1 Diabetes | Phase4 | Type 1 Diabetes Mellitus | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00157547 | Quantitative EEG (QEEG) as a Predictor of Treatment Outcome in Depression | Phase4 | Major Depressive Disorder | Completed | 2003-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00635843 | MAVERICK™ Total Disc Replacement- Pivotal Study | Phase3 | Spinal Diseases | Completed | 2003-04-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01491542 | INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolatera… | Na | Degenerative Disc Disease | Completed | 2003-04-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00251251 | Resynchronization/Defibrillation for Ambulatory Heart Failure Trial | Na | Heart Failure, Congestive | Completed | 2003-04-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00643279 | Chronicle Offers Management to Patients With Advanced Signs and Symptoms of Hea… | Na | Heart Failure | Completed | 2003-03-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00211211 | FREE Study - Fracture Reduction Evaluation | Phase4 | Osteopenia | Completed | 2003-02-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00298740 | Medtronic MiniMed Implantable Insulin Pump | Na | Type 1 Diabetes | Completed | 2003-02-01 | 2009-09-24 | ClinicalTrials.gov |
| NCT00132990 | A Multicenter Pilot Study of Pallidal Deep Brain Stimulation for Cervical Dysto… | Na | Cervical Dystonia | Completed | 2003-02-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00284830 | SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atr… | Na | Sick Sinus Syndrome | Completed | 2003-01-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00999089 | Arrested Versus Beating Heart Techniques in Coronary Revascularisation | Phase3 | Coronary Artery Bypass Grafting | Unknown | 2003-01-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00336011 | Safety of Cardiac Pacemakers in 1.5T Tesla MRI | — | Heart Diseases | Completed | 2002-12-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00200044 | An Evaluation of the Medtronic Gatekeeper System in the Treatment of SUBJECTS W… | Na | Gastroesophageal Reflux Disease | Terminated | 2002-12-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01069952 | Electrical Stimulation of the Internal Capsule for Intractable Depression | Phase2 | Depression | Completed | 2002-12-01 | — | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00759122 | Electroencephalography (EEG) Biomarkers of Response in Depression | Phase4 | Major Depressive Disorder | Completed | 2002-11-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00202358 | Perioperative Effect of Atenolol on Cytokine Profiles | Phase4 | Surgery | Unknown | 2002-11-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00294034 | VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New … | — | Pacemaker | Completed | 2002-10-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00142259 | Efficacy and Safety of DBS of the GPi in Patients With Primary Generalized and … | Phase4 | Dystonia | Unknown | 2002-10-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00642876 | PRESTIGE® Cervical Disc Study | Na | Degenerative Cervical Disc Disease | Completed | 2002-10-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00267137 | Study for Atrial Fibrillation Reduction (SAFARI) | Na | Atrial Fibrillation, Bradycardia | Completed | 2002-09-01 | 2006-07-21 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00266682 | Clinical Investigation of the SelectSecure Pacing Lead | Na | Bradycardia | Completed | 2002-08-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00120094 | International Study on Syncope of Uncertain Etiology | — | Syncope | Terminated | 2002-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00157755 | Enterra Therapy Clinical Study (Gastric Stimulation for Gastroparesis) | Na | Gastroparesis | Terminated | 2002-06-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00211536 | Study Comparing Effectiveness of Intraperitoneal Insulin Administration to Subc… | Phase3 | Type 1 Diabetes | Completed | 2002-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00170287 | SMS: Substrate Modification Study in Patients Getting an Implantable Cardiovert… | Phase4 | Tachycardia, Ventricular | Completed | 2002-05-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01491477 | INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical … | Na | Degenerative Cervical Disc Disease | Terminated | 2002-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00170261 | ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope | Phase4 | Syncope | Completed | 2002-04-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00203333 | Cardiac Rhythm Abnormalities in Patients With Refractory Epilepsy at High Risk … | — | Refractory Epilepsy | Completed | 2002-04-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01076452 | Phase II Subthalamic Nucleus (STN) vs. Globus Pallidus (GPi) Trial | Phase3 | Parkinson's Disease | Completed | 2002-04-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00707265 | rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study | Phase3 | Degenerative Disc Disease | Completed | 2002-03-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00273182 | InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | — | Heart Failure | Completed | 2002-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00525356 | INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dis… | Phase3 | Aortic Diseases | Completed | 2002-02-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00200057 | Sacral Nerve Stimulation Therapy for the Treatment of Chronic Fecal Incontinence | Na | Fecal Incontinence | Completed | 2002-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00367068 | Dutch National ITB Study in Children With Cerebral Palsy | Phase3 | Cerebral Palsy | Completed | 2002-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00657826 | ATS 3f(r) Aortic Bioprosthesis Model 1000, 19mm | Na | Heart Valve Diseases | Terminated | 2001-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00587444 | Optimal Heparin Dosing Regimens for Cardiopulmonary Bypass | Phase3 | Postoperative Hemorrhage | Completed | 2001-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00857662 | Study Comparing Onyx and TRUFILL in Brain Arteriovenous Malformations (AVMs) | Phase2 | Brain Arteriovenous Malformations | Completed | 2001-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01574625 | Post-Approval Study for the MOSAIC® Bioprostheses | — | Aortic Valve Stenosis and/or Insufficiency | Completed | 2001-04-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00170300 | Care-HF CArdiac Resynchronization in Heart Failure | Na | Heart Failure | Completed | 2001-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01061983 | Electrical Stimulation of the Internal Capsule for Intractable Obsessive-compul… | Phase2 | Obsessive-Compulsive Disorder | Completed | 2001-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00157820 | DATAS: The Dual Chamber & Atrial Tachyarrhythmias Adverse Events Study | Na | Ventricular Tachycardia | Completed | 2000-11-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT01494493 | Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Terminated | 2000-09-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00157742 | Comparison of SCS and PMR in Patients With Refractory Angina Pectoris | Phase4 | Angina Pectoris | Terminated | 2000-09-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00157781 | LEAF - Low Energy In Atrial Fibrillation | Phase4 | Atrial Fibrillation | Completed | 2000-08-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00170274 | APART: Prevention and Automatic Therapy of Atrial Arrhythmias in Patients With … | Na | Tachyarrhythmia | Completed | 2000-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00627328 | The Atrial High Rate Episodes in Pacemaker Patients | — | Arrhythmia | Completed | 2000-07-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00161538 | Pacing of the Atria in Sick Sinus Syndrome Trial Preventive Strategies for Atri… | Phase4 | Sick Sinus Syndrome | Completed | 2000-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01076361 | Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-app… | — | Arrhythmia | Completed | 1999-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01494454 | Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral L… | Na | Degenerative Disc Disease | Completed | 1999-08-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT00157768 | IRIS : Use of Implantable Defibrillator in High-risk Patients Early After Acute… | Phase4 | Acute Myocardial Infarction | Completed | 1999-06-09 | 2007-10-15 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491451 | A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar I… | Na | Degenerative Disc Disease | Completed | 1999-02-01 | 2003-01-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01491425 | A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fu… | Na | Degenerative Disc Disease | Completed | 1998-11-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00200005 | Sacral Nerve Stimulation for Anal Incontinence and Bowel Control | Phase4 | Fecal Incontinence and Constipation | Completed | 1998-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01491386 | Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusi… | Na | Degenerative Disc Disease | Completed | 1998-08-01 | 2002-10-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT01494428 | A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody… | Na | Degenerative Disc Disease | Completed | 1998-04-01 | 2004-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01495234 | Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instabilit… | Na | Degenerative Disc Disease | Completed | 1996-10-01 | 2001-06-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01076348 | Model 4965 Post-Approval Study | — | Heart Failure | Completed | 1996-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00620399 | A Study on the Use of a Brace Following Low Back Surgery | Phase3 | Lumbar Fusion | Completed | 1996-05-01 | 2003-06-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
| NCT00271180 | Product Performance Report: Evaluate Long-term Reliability & Performance of Med… | — | Arrhythmia | Recruiting | 1983-01-01 | 2040-12-01 | ClinicalTrials.gov |
Total clinical trials: 16742
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| Haemorrhoid artery embolizsation (HAE) | Other | Preclinical | Hemorrhoid | NOT_YET_RECRUITING | NCT07264413 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | COMPLETED | NCT07408141 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (DM) | NOT_YET_RECRUITING | NCT07675161 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Pipeline Embolization Device | Device | Preclinical | Brain Aneurysm | TERMINATED | NCT01557036 |
| Intrepid™ TTVR System | Other | Approved | Tricuspid Regurgitation | RECRUITING | NCT04433065 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Percept™ PC and Percept RC with Adaptive DBS (aDBS™) | Other | Approved | Parkinson's Disease | RECRUITING | NCT07216976 |
| Focal Radiotherapy | Drug | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Temozolomide | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Ritonavir | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Lamivudine | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Abacavir | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Magnetic Resonance (MR)-guided Laser Interstitial Thermal Therapy (LITT) | Drug | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| EndoFLIP | Other | Approved | Esophagogastric Junction Distensibility | ACTIVE_NOT_RECRUITING | NCT04450628 |
| Medtronic DBM | Other | Approved | Multi-Level Degenerative Lumbosacral Spinal Conditions | ACTIVE_NOT_RECRUITING | NCT03118505 |
| Infuse Bone Graft | Other | Approved | Multi-Level Degenerative Lumbosacral Spinal Conditions | ACTIVE_NOT_RECRUITING | NCT03118505 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| Onyx Drug Eluting Stent group | Drug | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT02593994 |
| Medtronic CoreValve® Evolut R System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| Conventional therapy | Drug | Approved | Acute Gastrointestinal Bleeding | RECRUITING | NCT06188585 |
| UI-EWD | Other | Approved | Acute Gastrointestinal Bleeding | RECRUITING | NCT06188585 |
| Standard Postoperative Care plus In-Bed Cycling | Other | Approved | Spine | RECRUITING | NCT07506720 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | RECRUITING | NCT07599904 |
| CINDY Virtual Reality Educational Intervention | Other | Approved | Healthy | RECRUITING | NCT07305714 |
| Sphere-9™ Catheter and Affera™ Ablation System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT06858306 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia (VT) | RECRUITING | NCT06703489 |
| Concerto Versa™ Detachable Coils | Other | Preclinical | Arteriovenous Malformation | NOT_YET_RECRUITING | NCT07639853 |
| Signia™ circular stapler with Tri-Staple™ Technology (Signia™ Circular Stapling system) | Other | Approved | Colorectal Anastomosis | RECRUITING | NCT07351071 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Intraoperative Computed Tomography (O-arm) | Other | Preclinical | Degenerative Lumbar Spine Diseases | NOT_YET_RECRUITING | NCT07644507 |
| Sham Procedure | Procedure | Approved | Hypertension | COMPLETED | NCT02439775 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | COMPLETED | NCT02439775 |
| Concerto Versa™ Detachable Coils | Other | Preclinical | Arteriovenous Malformation | NOT_YET_RECRUITING | NCT07639853 |
| MiniMed™ NMX8-AID System with DS5™/Simplera Sync™ | Other | Approved | Type 1 Diabetes Mellitus | RECRUITING | NCT07228117 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | RECRUITING | NCT07335341 |
| Medtronic SenSight Directional DBS lead | Other | Phase PHASE1 | Treatment Resistant Depression | RECRUITING | NCT06096207 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| MRI guided laser ablation | Other | Approved | Neoplasm Metastasis | RECRUITING | NCT05023772 |
| Stereotactic Radiosurgery | Procedure | Approved | Neoplasm Metastasis | RECRUITING | NCT05023772 |
| Stereotactic Laser Ablation | Other | Approved | Neoplasm Metastasis | RECRUITING | NCT05023772 |
| Edwards SAPIEN 3 or SAPIEN 3 Ultra THV Systems | Other | Approved | Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04722250 |
| Medtronic Evolut PRO, Evolut PRO+ or Evolut FX (where commercially available) TAV Systems | Other | Approved | Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04722250 |
| Harmony TPV System | Other | Approved | Congenital Heart Disease | ACTIVE_NOT_RECRUITING | NCT05077774 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| Endurant Chimney Graft Technique | Other | Preclinical | AAA - Abdominal Aortic Aneurysm | ACTIVE_NOT_RECRUITING | NCT03320252 |
| Robotic Assisted-Surgery (RAS) Hysterectomy | Procedure | Approved | Uterine Fibroids (UF) | ACTIVE_NOT_RECRUITING | NCT07120945 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic SenSight Directional DBS lead | Other | Phase PHASE1 | Treatment Resistant Depression | RECRUITING | NCT06096207 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Edwards TAV | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06777368 |
| Medtronic TAV | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06777368 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | ACTIVE_NOT_RECRUITING | NCT07408141 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | ACTIVE_NOT_RECRUITING | NCT04735016 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | ACTIVE_NOT_RECRUITING | NCT07408141 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | ACTIVE_NOT_RECRUITING | NCT04735016 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | ACTIVE_NOT_RECRUITING | NCT07408141 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | ACTIVE_NOT_RECRUITING | NCT04735016 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | ACTIVE_NOT_RECRUITING | NCT07408141 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | ACTIVE_NOT_RECRUITING | NCT04735016 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | ACTIVE_NOT_RECRUITING | NCT07408141 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | ACTIVE_NOT_RECRUITING | NCT04735016 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | ACTIVE_NOT_RECRUITING | NCT07408141 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | ACTIVE_NOT_RECRUITING | NCT04735016 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | ACTIVE_NOT_RECRUITING | NCT07408141 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | ACTIVE_NOT_RECRUITING | NCT04735016 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Arctic Front™ Cardiac Cryoablation Catheter System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT05005949 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Automated insulin delivery system - Medtronic 780G | Other | Approved | Pregnancy | NOT_YET_RECRUITING | NCT07602036 |
| FEVAR treatment : Fenestrated endograft | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| ESAR treatment: Endograft + Heli-FX Endoanchor | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Arctic Front™ Cardiac Cryoablation Catheter System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT05005949 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Automated insulin delivery system - Medtronic 780G | Other | Approved | Pregnancy | NOT_YET_RECRUITING | NCT07602036 |
| FEVAR treatment : Fenestrated endograft | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| ESAR treatment: Endograft + Heli-FX Endoanchor | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Arctic Front™ Cardiac Cryoablation Catheter System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT05005949 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Automated insulin delivery system - Medtronic 780G | Other | Approved | Pregnancy | NOT_YET_RECRUITING | NCT07602036 |
| FEVAR treatment : Fenestrated endograft | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| ESAR treatment: Endograft + Heli-FX Endoanchor | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Arctic Front™ Cardiac Cryoablation Catheter System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT05005949 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Automated insulin delivery system - Medtronic 780G | Other | Approved | Pregnancy | NOT_YET_RECRUITING | NCT07602036 |
| FEVAR treatment : Fenestrated endograft | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| ESAR treatment: Endograft + Heli-FX Endoanchor | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Arctic Front™ Cardiac Cryoablation Catheter System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT05005949 |
| Treatment of Intracranial Aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT06604884 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Automated insulin delivery system - Medtronic 780G | Other | Approved | Pregnancy | NOT_YET_RECRUITING | NCT07602036 |
| FEVAR treatment : Fenestrated endograft | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| ESAR treatment: Endograft + Heli-FX Endoanchor | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Device: Mechanical Thrombectomy | Device | Preclinical | Acute Ischemic Stroke | NOT_YET_RECRUITING | NCT07599904 |
| Hyperangulated videolaryngoscopy | Other | Approved | Intubation Skill | NOT_YET_RECRUITING | NCT07600502 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| Sphere-360 Pulsed Field Ablation Catheter with the Affera Mapping and Ablation System | Other | Approved | Paroxysmal AF | RECRUITING | NCT07308847 |
| Standard lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Personalized lower rate pacing | Other | Approved | Bradycardia | NOT_YET_RECRUITING | NCT07589452 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| MiniMed™ NMX8-AID System with DS5™ | Other | Approved | Type 1 Diabetes Mellitus | RECRUITING | NCT07228117 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| ACDF interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Titan nanoLOCK interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Emprint Microwave Ablation System | Other | Preclinical | Colorectal Neoplasms Malignant | COMPLETED | NCT03775980 |
| MiniMed™ NMX8-AID System with DS5™ | Other | Approved | Type 1 Diabetes Mellitus | RECRUITING | NCT07228117 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia | NOT_YET_RECRUITING | NCT07585968 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| ACDF interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Titan nanoLOCK interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Observational | Other | Preclinical | Tissue Oxygenation | COMPLETED | NCT07166341 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Emprint Microwave Ablation System | Other | Preclinical | Colorectal Neoplasms Malignant | COMPLETED | NCT03775980 |
| Traditional Laparoscopic Cholecystectomy (TLC) | Other | Approved | Biliary Dyskinesia | TERMINATED | NCT01195285 |
| Single-Incision Laparoscopic Surgery cholecystectomy | Procedure | Approved | Biliary Dyskinesia | TERMINATED | NCT01195285 |
| Traditional Laparoscopic Cholecystectomy (TLC) | Other | Approved | Biliary Dyskinesia | TERMINATED | NCT01195285 |
| Single-Incision Laparoscopic Surgery cholecystectomy | Procedure | Approved | Biliary Dyskinesia | TERMINATED | NCT01195285 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| ACDF interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Titan nanoLOCK interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Emprint Microwave Ablation System | Other | Preclinical | Colorectal Neoplasms Malignant | COMPLETED | NCT03775980 |
| MiniMed™ NMX8-AID System with DS5™ | Other | Approved | Type 1 Diabetes Mellitus | RECRUITING | NCT07228117 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| ACDF interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Titan nanoLOCK interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Emprint Microwave Ablation System | Other | Preclinical | Colorectal Neoplasms Malignant | COMPLETED | NCT03775980 |
| MiniMed™ NMX8-AID System with DS5™ | Other | Approved | Type 1 Diabetes Mellitus | RECRUITING | NCT07228117 |
| HALO90 Ablation catheter | Other | Approved | Pelvic Neoplasms | COMPLETED | NCT01103492 |
| HALO90 Ablation catheter | Other | Approved | Pelvic Neoplasms | COMPLETED | NCT01103492 |
| HALO90 Ablation catheter | Other | Approved | Pelvic Neoplasms | COMPLETED | NCT01103492 |
| Capnographic monitoring | Other | Approved | Capnography | UNKNOWN | NCT03025490 |
| Capnographic monitoring | Other | Approved | Capnography | UNKNOWN | NCT03025490 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| ACDF interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Titan nanoLOCK interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Emprint Microwave Ablation System | Other | Preclinical | Colorectal Neoplasms Malignant | COMPLETED | NCT03775980 |
| MiniMed™ NMX8-AID System with DS5™ | Other | Approved | Type 1 Diabetes Mellitus | RECRUITING | NCT07228117 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | RECRUITING | NCT07335341 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| ACDF interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Titan nanoLOCK interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Conventional CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| MICS CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| Emprint Microwave Ablation System | Other | Preclinical | Colorectal Neoplasms Malignant | COMPLETED | NCT03775980 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| MiniMed™ NMX8-AID System with DS5™ | Other | Approved | Type 1 Diabetes Mellitus | RECRUITING | NCT07228117 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| Conventional CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| MICS CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | RECRUITING | NCT07335341 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| Conventional CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| MICS CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | RECRUITING | NCT07335341 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| Conventional CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| MICS CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | RECRUITING | NCT07335341 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| Conventional CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| MICS CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | RECRUITING | NCT07335341 |
| Altaviva™ system | Other | Approved | Urge Urinary Incontinence | RECRUITING | NCT07456865 |
| Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Procedure | Approved | Spinal Deformity | RECRUITING | NCT05856370 |
| endosuture aneurysm repair (ESAR) using Heli-FX EndoAnchor system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endovascular aneurysm repair (EVAR) using the Endurant II/IIs stent graft system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| Conventional CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| MICS CABG | Other | Approved | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT03447938 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | RECRUITING | NCT07335341 |
| endosuture aneurysm repair (ESAR) using Heli-FX EndoAnchor system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endovascular aneurysm repair (EVAR) using the Endurant II/IIs stent graft system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endosuture aneurysm repair (ESAR) using Heli-FX EndoAnchor system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endovascular aneurysm repair (EVAR) using the Endurant II/IIs stent graft system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endosuture aneurysm repair (ESAR) using Heli-FX EndoAnchor system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endovascular aneurysm repair (EVAR) using the Endurant II/IIs stent graft system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endosuture aneurysm repair (ESAR) using Heli-FX EndoAnchor system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endovascular aneurysm repair (EVAR) using the Endurant II/IIs stent graft system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endosuture aneurysm repair (ESAR) using Heli-FX EndoAnchor system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endovascular aneurysm repair (EVAR) using the Endurant II/IIs stent graft system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| Sphere-9™ Catheter and Affera™ Ablation System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT06858306 |
| PulseSelect Pulse Field Ablation (PFA) System | Other | Approved | Paroxysmal Atrial Fibrillation (PAF) | NOT_YET_RECRUITING | NCT07575828 |
| Gatekeeper Reflux Repair System | Other | Approved | Gastroesophageal Reflux Disease | TERMINATED | NCT00200044 |
| Guardian RT Telemetered Glucose Monitoring System | Other | Phase PHASE4 | Type 1 Diabetes Mellitus | COMPLETED | NCT01331343 |
| Guardian RT Telemetered Glucose Monitoring System | Other | Phase PHASE4 | Type 1 Diabetes Mellitus | COMPLETED | NCT01331343 |
| Biventricular Pacing (DDD(R)- BiV) | Other | Phase PHASE4 | Atrioventricular Block | WITHDRAWN | NCT00559143 |
| Biventricular Pacing (DDD(R)- BiV) | Other | Phase PHASE4 | Atrioventricular Block | WITHDRAWN | NCT00559143 |
| Non-surgical Treatment | Drug | Approved | Multiple Myeloma | WITHDRAWN | NCT01175278 |
| Vertebral Augmentation with Balloon Kyphoplasty | Other | Approved | Multiple Myeloma | WITHDRAWN | NCT01175278 |
| Non-surgical Treatment | Drug | Approved | Multiple Myeloma | WITHDRAWN | NCT01175278 |
| Vertebral Augmentation with Balloon Kyphoplasty | Other | Approved | Multiple Myeloma | WITHDRAWN | NCT01175278 |
| Non-surgical Treatment | Drug | Approved | Multiple Myeloma | WITHDRAWN | NCT01175278 |
| Vertebral Augmentation with Balloon Kyphoplasty | Other | Approved | Multiple Myeloma | WITHDRAWN | NCT01175278 |
| Mechanical ventilation mode (PAV+ vs. ACV) | Other | Phase PHASE4 | Respiratory Failure | COMPLETED | NCT01204281 |
| Mechanical ventilation mode (PAV+ vs. ACV) | Other | Phase PHASE4 | Respiratory Failure | COMPLETED | NCT01204281 |
| Integrated sensor and infusion set. | Other | Approved | Diabetes Type 1 | COMPLETED | NCT01770561 |
| Endeavor Resolute Zotarolimus-Eluting Coronary Stent System | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT00752128 |
| Endeavor Resolute Zotarolimus-Eluting Coronary Stent System | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT00752128 |
| Control group training without Guided Exercise system at home | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01761448 |
| Guided Exercise Training with an easy to wear vest with electrodes to measure ECG, respiration, activity | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01761448 |
| Guide Exercise (GEx-)- Training | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01761448 |
| Pulmonary vein isolation | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT02051621 |
| Cavo-tricuspid-isthmus-ablation | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT02051621 |
| Antiarrhythmic drug | Drug | Approved | Atrial Fibrillation | UNKNOWN | NCT02051621 |
| Capsule endoscopy | Other | Phase EARLY_PHASE1 | Lynch Syndrome | COMPLETED | NCT00898768 |
| Activa RC | Other | Phase PHASE4 | Parkinson's Disease | COMPLETED | NCT00998660 |
| Renal Denervation (Symplicity® Renal Denervation System) | Other | Approved | Uncontrolled Hypertension | COMPLETED | NCT00888433 |
| Renal Denervation (Symplicity® Renal Denervation System) | Other | Approved | Uncontrolled Hypertension | COMPLETED | NCT00888433 |
| Renal Denervation (Symplicity® Renal Denervation System) | Other | Approved | Uncontrolled Hypertension | COMPLETED | NCT00888433 |
| Sphere-9™ Catheter and Affera™ Ablation System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT06858306 |
| PulseSelect Pulse Field Ablation (PFA) System | Other | Approved | Paroxysmal Atrial Fibrillation (PAF) | NOT_YET_RECRUITING | NCT07575828 |
| Sphere-9™ Catheter and Affera™ Ablation System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT06858306 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Device | Device | Preclinical | Arrhythmia | RECRUITING | NCT00271180 |
| PulseSelect Pulse Field Ablation (PFA) System | Other | Approved | Paroxysmal Atrial Fibrillation (PAF) | NOT_YET_RECRUITING | NCT07575828 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Sphere-9™ Catheter and Affera™ Ablation System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT06858306 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Device | Device | Preclinical | Arrhythmia | RECRUITING | NCT00271180 |
| PulseSelect Pulse Field Ablation (PFA) System | Other | Approved | Paroxysmal Atrial Fibrillation (PAF) | NOT_YET_RECRUITING | NCT07575828 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Device | Device | Preclinical | Arrhythmia | RECRUITING | NCT00271180 |
| PulseSelect Pulse Field Ablation (PFA) System | Other | Approved | Paroxysmal Atrial Fibrillation (PAF) | NOT_YET_RECRUITING | NCT07575828 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Device | Device | Preclinical | Arrhythmia | RECRUITING | NCT00271180 |
| Medtronic ICDs, CRT-Ds, and CRT-Ps | Other | Preclinical | Heart Failure; With Decompensation | COMPLETED | NCT02134379 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Device | Device | Preclinical | Arrhythmia | RECRUITING | NCT00271180 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Device | Device | Preclinical | Arrhythmia | RECRUITING | NCT00271180 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | RECRUITING | NCT07115953 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | RECRUITING | NCT05822895 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | RECRUITING | NCT07507422 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | RECRUITING | NCT07223008 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Renal nerve stimulation | Other | Approved | Hypertension | RECRUITING | NCT07013929 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | ACTIVE_NOT_RECRUITING | NCT05294445 |
| ATS Medical 3f® Aortic Bioprosthesis, Model 1000 19mm | Other | Preclinical | Heart Valve Diseases | WITHDRAWN | NCT01156272 |
| Medtronic Talent Stent-Graft-System | Other | Phase PHASE3 | Aortic Diseases | COMPLETED | NCT00525356 |
| Medtronic Talent Stent-Graft-System | Other | Phase PHASE3 | Aortic Diseases | COMPLETED | NCT00525356 |
| LV Lead Extraction | Other | Preclinical | Heart Failure | COMPLETED | NCT00893386 |
| LV Lead Extraction | Other | Preclinical | Heart Failure | COMPLETED | NCT00893386 |
| Insertable Cardiac Monitor Implant | Other | Approved | Syncope | COMPLETED | NCT01965899 |
| Standard of Care | Other | Phase PHASE4 | Chagas Disease | TERMINATED | NCT01539161 |
| Implantable Cardiac Monitor | Other | Phase PHASE4 | Chagas Disease | TERMINATED | NCT01539161 |
| Standard of Care | Other | Phase PHASE4 | Chagas Disease | TERMINATED | NCT01539161 |
| Implantable Cardiac Monitor | Other | Phase PHASE4 | Chagas Disease | TERMINATED | NCT01539161 |
| Standard of Care | Other | Phase PHASE4 | Chagas Disease | TERMINATED | NCT01539161 |
| Implantable Cardiac Monitor | Other | Phase PHASE4 | Chagas Disease | TERMINATED | NCT01539161 |
| Burke-Fahn- Marsden scale | Other | Preclinical | Dystonia | COMPLETED | NCT02468843 |
| Unified Dystonia Rating Scale | Other | Preclinical | Dystonia | COMPLETED | NCT02468843 |
| Biphasic DBS stimulation | Other | Preclinical | Dystonia | COMPLETED | NCT02468843 |
| Low weight polypropylene mesh | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00827944 |
| Parietex Progrip | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00827944 |
| Low weight polypropylene mesh | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00827944 |
| Parietex Progrip | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00827944 |
| Symplicity renal denervation system | Other | Approved | Adults With Uncontrolled Hypertension | TERMINATED | NCT01632943 |
| Multiple daily injections of insulin | Other | Phase PHASE4 | Type 2 Diabetes Mellitus | UNKNOWN | NCT03112538 |
| Insulin Pump | Other | Phase PHASE4 | Type 2 Diabetes Mellitus | UNKNOWN | NCT03112538 |
| Traditional sterilization | Other | Approved | Sterilization, Tubal | COMPLETED | NCT02165709 |
| Salpingectomy | Other | Approved | Sterilization, Tubal | COMPLETED | NCT02165709 |
| Traditional sterilization | Other | Approved | Sterilization, Tubal | COMPLETED | NCT02165709 |
| Salpingectomy | Other | Approved | Sterilization, Tubal | COMPLETED | NCT02165709 |
| Motion | Other | Phase PHASE3 | Healthy | COMPLETED | NCT02247765 |
| Arterial line | Other | Phase PHASE3 | Healthy | COMPLETED | NCT02247765 |
| Motion | Other | Phase PHASE3 | Healthy | COMPLETED | NCT02247765 |
| Arterial line | Other | Phase PHASE3 | Healthy | COMPLETED | NCT02247765 |
| Closed Loop Procedure (Medtronic) | Procedure | Approved | Type 1 Diabetes | COMPLETED | NCT01712594 |
| Closed Loop Procedure (Medtronic) | Procedure | Approved | Type 1 Diabetes | COMPLETED | NCT01712594 |
| REVEAL Implantable Cardiac Monitor | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01727297 |
| REVEAL Implantable Cardiac Monitor | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01727297 |
| MiniMed Paradigm REAL-Time System | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00417989 |
| MiniMed Paradigm REAL-Time System | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00417989 |
| Oblique Lateral Interbody Fusion | Other | Preclinical | Degenerative Disc Disease | TERMINATED | NCT02657421 |
| Oblique Lateral Interbody Fusion | Other | Preclinical | Degenerative Disc Disease | TERMINATED | NCT02657421 |
| 530G Insulin pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02120794 |
| 530G Insulin pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02120794 |
| Magnetic Resonance Imaging (MRI) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01520532 |
| Optimized Medical Management | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01711619 |
| subcutaneous nerve stimulation | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01711619 |
| Optimized Medical Management | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01711619 |
| subcutaneous nerve stimulation | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01711619 |
| 3D high resolution anorectal manometry | Other | Approved | Children | COMPLETED | NCT02296008 |
| Barrel™ Vascular Reconstruction Device (VRD) | Device | Approved | Intracranial Aneurysms | COMPLETED | NCT02125097 |
| Barrel™ Vascular Reconstruction Device (VRD) | Device | Approved | Intracranial Aneurysms | COMPLETED | NCT02125097 |
| Resolute Integrity Stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01638507 |
| Resolute Integrity Stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01638507 |
| interview regarding goals | Other | Preclinical | Failed Back Surgery Syndrome | COMPLETED | NCT03761316 |
| PlasmaBlade 3.0S | Other | Approved | Breast Cancer | COMPLETED | NCT03711916 |
| PillCam™ (Capsule Endoscopy) Colon 2 capsule | Other | Phase PHASE3 | Colonic Diseases | COMPLETED | NCT01063231 |
| PillCam ESO2 | Other | Approved | Upper Gastrointestinal Hemorrhage | COMPLETED | NCT00974701 |
| PillCam ESO2 | Other | Approved | Upper Gastrointestinal Hemorrhage | COMPLETED | NCT00974701 |
| Reveal LINQ™ Insertable Cardiac Monitor (ICM) | Other | Preclinical | Heart Failure | COMPLETED | NCT02758301 |
| superDimension™ Navigation System Version 7.2 | Other | Approved | Lung Cancer | COMPLETED | NCT03585959 |
| superDimension™ Navigation System Version 7.2 | Other | Approved | Lung Cancer | COMPLETED | NCT03585959 |
| Invasive Arm | Other | Approved | Acute Coronary Syndromes | COMPLETED | NCT02086019 |
| Conservative Arm | Other | Approved | Acute Coronary Syndromes | COMPLETED | NCT02086019 |
| Invasive Arm | Other | Approved | Acute Coronary Syndromes | COMPLETED | NCT02086019 |
| Conservative Arm | Other | Approved | Acute Coronary Syndromes | COMPLETED | NCT02086019 |
| Invasive Arm | Other | Approved | Acute Coronary Syndromes | COMPLETED | NCT02086019 |
| Conservative Arm | Other | Approved | Acute Coronary Syndromes | COMPLETED | NCT02086019 |
| spinal cord stimulation | Other | Preclinical | Failed Back Surgery Syndrome | COMPLETED | NCT02787265 |
| Permacol Paste | Other | Preclinical | Crohn Disease | UNKNOWN | NCT03776825 |
| Implantable devices working as neurostimulators, stents, spinal/bone devices or other applications | Device | Preclinical | Arrhythmias, Cardiac | WITHDRAWN | NCT01007474 |
| Cardiac Resynchronization Therapy-Defibrillator (CRT-D) | Drug | Preclinical | Arrhythmias, Cardiac | WITHDRAWN | NCT01007474 |
| Implantable Loop Recorder (ILR) | Other | Preclinical | Arrhythmias, Cardiac | WITHDRAWN | NCT01007474 |
| Implantable Pacemaker Generator (IPG) | Other | Preclinical | Arrhythmias, Cardiac | WITHDRAWN | NCT01007474 |
| Implantable Cardioverter-Defibrillator (ICD) | Other | Preclinical | Arrhythmias, Cardiac | WITHDRAWN | NCT01007474 |
| Lymphadenectomy | Other | Approved | Lung Neoplasm Malignant | UNKNOWN | NCT04778826 |
| Axys EX device | Device | Approved | Peripheral Arterial Disease | WITHDRAWN | NCT04282161 |
| Non-Invasive Controlled Hypoxia | Other | Preclinical | Hypoxia | COMPLETED | NCT04811963 |
| Non-Invasive Controlled Hypoxia | Other | Preclinical | Hypoxia | COMPLETED | NCT04811963 |
| MicroFx™ PGLA COILS | Other | Preclinical | Intracranial Aneurysm | WITHDRAWN | NCT01194388 |
| MicroFx™ PGLA COILS | Other | Preclinical | Intracranial Aneurysm | WITHDRAWN | NCT01194388 |
| MicroFx™ PGLA COILS | Other | Preclinical | Intracranial Aneurysm | WITHDRAWN | NCT01194388 |
| Guardian™ Sensor (3) connected to a Guardian™ Connect Transmitter | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT03966911 |
| Talent Abdominal Stent Graft | Other | Approved | Aortic Aneurysm, Abdominal | COMPLETED | NCT00816062 |
| Protack™ | Other | Approved | Incisional Hernia | COMPLETED | NCT03434301 |
| ReliaTack™ | Other | Approved | Incisional Hernia | COMPLETED | NCT03434301 |
| Endurant Stent Graft | Other | Preclinical | Aortic Aneurysm, Abdominal | COMPLETED | NCT00870051 |
| Endurant Stent Graft | Other | Preclinical | Aortic Aneurysm, Abdominal | COMPLETED | NCT00870051 |
| ABI | Other | Preclinical | Critical Limb Ischemia | UNKNOWN | NCT05455554 |
| Flowmet-D | Other | Preclinical | Critical Limb Ischemia | UNKNOWN | NCT05455554 |
| ABI | Other | Preclinical | Critical Limb Ischemia | UNKNOWN | NCT05455554 |
| Flowmet-D | Other | Preclinical | Critical Limb Ischemia | UNKNOWN | NCT05455554 |
| Sublingual microscopy | Other | Approved | Heart Diseases | COMPLETED | NCT04058860 |
| Cox monitoring | Other | Approved | Heart Diseases | COMPLETED | NCT04058860 |
| NIRS monitoring | Other | Approved | Heart Diseases | COMPLETED | NCT04058860 |
| Sublingual microscopy | Other | Approved | Heart Diseases | COMPLETED | NCT04058860 |
| Cox monitoring | Other | Approved | Heart Diseases | COMPLETED | NCT04058860 |
| NIRS monitoring | Other | Approved | Heart Diseases | COMPLETED | NCT04058860 |
| No AAD post Ablation. | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02913014 |
| CAPERE Thrombectomy System | Other | Approved | Arteriovenous Graft Thrombosis | TERMINATED | NCT04494035 |
| CAPERE Thrombectomy System | Other | Approved | Arteriovenous Graft Thrombosis | TERMINATED | NCT04494035 |
| Accelerometer Sensing for Micra AV Study | Other | Approved | AV Block | COMPLETED | NCT04245345 |
| Stress Test | Other | Preclinical | Exercise | TERMINATED | NCT03859167 |
| Standard of Care | Other | Approved | Upper Gastrointestinal Bleeding | COMPLETED | NCT03458000 |
| PillCam UGI | Other | Approved | Upper Gastrointestinal Bleeding | COMPLETED | NCT03458000 |
| Diagnostic Colonoscopy | Other | Approved | Colonic Polyp | COMPLETED | NCT04723758 |
| GI Genius-assisted diagnostic colonoscopy | Other | Approved | Colonic Polyp | COMPLETED | NCT04723758 |
| Investigational RAMware downloaded onto Reveal LINQ device | Device | Preclinical | Respiratory Rate | COMPLETED | NCT04506684 |
| Investigational RAMware downloaded onto Reveal LINQ device | Device | Preclinical | Respiratory Rate | COMPLETED | NCT04506684 |
| Investigational RAMware downloaded onto Reveal LINQ device | Device | Preclinical | Respiratory Rate | COMPLETED | NCT04506684 |
| InPen with Guardian 4 System | Other | Approved | Diabetes Type 1 | COMPLETED | NCT05029271 |
| InPen with Guardian 4 System | Other | Approved | Diabetes Type 1 | COMPLETED | NCT05029271 |
| Medtronic Reveal LINQ™ Insertable Cardiac Monitor (ICM) | Other | Approved | Chronic Total Occlusion of Coronary Artery | COMPLETED | NCT03475888 |
| Mosaic model 305, model 310, and ultra model 305 | Other | Preclinical | Heart Valve Diseases | COMPLETED | NCT03139721 |
| Mosaic model 305, model 310, and ultra model 305 | Other | Preclinical | Heart Valve Diseases | COMPLETED | NCT03139721 |
| Responsive Brain Stimulation (RBS Setting) | Other | Approved | Tourette Syndrome | COMPLETED | NCT02056873 |
| Continuous DBS | Other | Approved | Tourette Syndrome | COMPLETED | NCT02056873 |
| High Density Programming | Other | Approved | Neuropathic Pain | COMPLETED | NCT03716973 |
| InterStim Micro | Other | Approved | Overactive Bladder | TERMINATED | NCT04506866 |
| InterStim Micro | Other | Approved | Overactive Bladder | TERMINATED | NCT04506866 |
| InterStim Micro | Other | Approved | Overactive Bladder | TERMINATED | NCT04506866 |
| MiniMed 780G System | Other | Approved | Type 1 Diabetes | COMPLETED | NCT05325294 |
| Medtronic PulseSelect Pulsed Field Ablation (PFA) System | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04198701 |
| Medtronic PulseSelect Pulsed Field Ablation (PFA) System | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04198701 |
| Holter monitoring | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02213731 |
| Antiarrhythmic Drugs | Drug | Phase PHASE4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | COMPLETED | NCT01803438 |
| cryoballoon ablation system | Other | Phase PHASE4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | COMPLETED | NCT01803438 |
| Antiarrhythmic Drugs | Drug | Phase PHASE4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | COMPLETED | NCT01803438 |
| cryoballoon ablation system | Other | Phase PHASE4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | COMPLETED | NCT01803438 |
| Antiarrhythmic Drugs | Drug | Phase PHASE4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | COMPLETED | NCT01803438 |
| cryoballoon ablation system | Other | Phase PHASE4 | Symptomatic Paroxysmal Atrial Fibrillation Without Clinically Significant Heart Diseases | COMPLETED | NCT01803438 |
| Pill-in-pocket anticoagulation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT06922695 |
| In office standard visit | Other | Approved | Arrhythmia | COMPLETED | NCT03125382 |
| Carelink System | Other | Approved | Arrhythmia | COMPLETED | NCT03125382 |
| In office standard visit | Other | Approved | Arrhythmia | COMPLETED | NCT03125382 |
| Carelink System | Other | Approved | Arrhythmia | COMPLETED | NCT03125382 |
| In office standard visit | Other | Approved | Arrhythmia | COMPLETED | NCT03125382 |
| Carelink System | Other | Approved | Arrhythmia | COMPLETED | NCT03125382 |
| Implantable Cardiac Defibrillator, Cardiac Resynchronization Therapy Defibrillator/Pacemaker | Drug | Preclinical | Heart Failure | COMPLETED | NCT03009175 |
| Implantable Cardiac Defibrillator, Cardiac Resynchronization Therapy Defibrillator/Pacemaker | Drug | Preclinical | Heart Failure | COMPLETED | NCT03009175 |
| Deep Brain Stimulation | Other | Phase PHASE1 | Tremor | RECRUITING | NCT07049003 |
| Observational | Other | Preclinical | Oxygen Saturation | COMPLETED | NCT06581835 |
| HeartWare Ventricular Assist Device | Device | Preclinical | Chronic Heart Failure | ACTIVE_NOT_RECRUITING | NCT03681210 |
| Endurant Chimney Graft Technique | Other | Preclinical | AAA - Abdominal Aortic Aneurysm | ACTIVE_NOT_RECRUITING | NCT03320252 |
| Endurant Chimney Graft Technique | Other | Preclinical | AAA - Abdominal Aortic Aneurysm | ACTIVE_NOT_RECRUITING | NCT03320252 |
| Medtronic Manufactured Spinal Cord Stimulators | Other | Phase PHASE1 | Chronic Pain in the Trunk and Limbs | UNKNOWN | NCT00351208 |
| Medtronic Manufactured Spinal Cord Stimulators | Other | Phase PHASE1 | Chronic Pain in the Trunk and Limbs | UNKNOWN | NCT00351208 |
| Implantable Pulse Generator | Other | Approved | Pacemaker | COMPLETED | NCT00307073 |
| Implantable Pulse Generator | Other | Approved | Pacemaker | COMPLETED | NCT00307073 |
| Implantable Cardioverter Defibrillator | Other | Approved | Ventricular Arrhythmias | COMPLETED | NCT00273195 |
| Implantable Cardioverter Defibrillator | Other | Approved | Ventricular Arrhythmias | COMPLETED | NCT00273195 |
| Pacing Lead | Other | Approved | Bradycardia | COMPLETED | NCT00266682 |
| Pacing Lead | Other | Approved | Bradycardia | COMPLETED | NCT00266682 |
| Selection 9000 prevent AF an Diagnose AF | Other | Phase PHASE4 | Sick Sinus Syndrome | COMPLETED | NCT00161538 |
| Pacing leads to be implanted according randomization. | Other | Phase PHASE4 | Sick Sinus Syndrome | COMPLETED | NCT00161538 |
| Selection 9000 prevent AF an Diagnose AF | Other | Phase PHASE4 | Sick Sinus Syndrome | COMPLETED | NCT00161538 |
| Pacing leads to be implanted according randomization. | Other | Phase PHASE4 | Sick Sinus Syndrome | COMPLETED | NCT00161538 |
| Pillar Palatal Implants | Other | Phase PHASE4 | Obstructive Sleep Apnea | COMPLETED | NCT00307957 |
| Pillar Palatal Implants | Other | Phase PHASE4 | Obstructive Sleep Apnea | COMPLETED | NCT00307957 |
| Pillar Palatal Implants | Other | Phase PHASE4 | Obstructive Sleep Apnea | COMPLETED | NCT00307957 |
| Implantable Pulse Generators | Other | Approved | Sick Sinus Syndrome | COMPLETED | NCT00284830 |
| Implantable Pulse Generators | Other | Approved | Sick Sinus Syndrome | COMPLETED | NCT00284830 |
| Implantable Pulse Generators | Other | Approved | Sick Sinus Syndrome | COMPLETED | NCT00284830 |
| Selective serotonin reuptake inhibitors (SSRI) | Other | Phase PHASE4 | Major Depressive Disorder | COMPLETED | NCT00157547 |
| Selective serotonin reuptake inhibitors (SSRI) | Other | Phase PHASE4 | Major Depressive Disorder | COMPLETED | NCT00157547 |
| placebo | Other | Phase PHASE4 | Surgery | UNKNOWN | NCT00202358 |
| atenolol | Other | Phase PHASE4 | Surgery | UNKNOWN | NCT00202358 |
| placebo | Other | Phase PHASE4 | Surgery | UNKNOWN | NCT00202358 |
| atenolol | Other | Phase PHASE4 | Surgery | UNKNOWN | NCT00202358 |
| placebo | Other | Phase PHASE4 | Surgery | UNKNOWN | NCT00202358 |
| atenolol | Other | Phase PHASE4 | Surgery | UNKNOWN | NCT00202358 |
| Gatekeeper Reflux Repari System (Device) | Device | Preclinical | GERD | TERMINATED | NCT00229086 |
| Gatekeeper Reflux Repari System (Device) | Device | Preclinical | GERD | TERMINATED | NCT00229086 |
| placebo | Other | Phase PHASE4 | Major Depressive Disorder | COMPLETED | NCT00759122 |
| venlafaxine (Effexor) | Other | Phase PHASE4 | Major Depressive Disorder | COMPLETED | NCT00759122 |
| placebo | Other | Phase PHASE4 | Major Depressive Disorder | COMPLETED | NCT00759122 |
| venlafaxine (Effexor) | Other | Phase PHASE4 | Major Depressive Disorder | COMPLETED | NCT00759122 |
| Vitatron biventricular pacemaker | Other | Phase PHASE4 | Congestive Heart Failure, Atrial Fibrillation | COMPLETED | NCT00156728 |
| Vitatron biventricular pacemaker | Other | Phase PHASE4 | Congestive Heart Failure, Atrial Fibrillation | COMPLETED | NCT00156728 |
| Pacing Lead | Other | Approved | Heart Failure | COMPLETED | NCT00269230 |
| Pacing Lead | Other | Approved | Heart Failure | COMPLETED | NCT00269230 |
| Spinal Cord Stimulation | Other | Phase PHASE4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | COMPLETED | NCT00200122 |
| Spinal Cord Stimulation | Other | Phase PHASE4 | Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome | COMPLETED | NCT00200122 |
| Enterra Therapy System (H9900014) | Drug | Approved | Severe to Morbid Obesity and Type 2 Diabetes | COMPLETED | NCT00200018 |
| Enterra Therapy System (H9900014) | Drug | Approved | Severe to Morbid Obesity and Type 2 Diabetes | COMPLETED | NCT00200018 |
| placebo | Other | Phase PHASE2 | Crohns Disease | UNKNOWN | NCT00731172 |
| glatiramer acetate | Other | Phase PHASE2 | Crohns Disease | UNKNOWN | NCT00731172 |
| placebo | Other | Phase PHASE2 | Crohns Disease | UNKNOWN | NCT00731172 |
| glatiramer acetate | Other | Phase PHASE2 | Crohns Disease | UNKNOWN | NCT00731172 |
| The Medtronic CareLink system (Minneapolis, MN, USA). | Other | Preclinical | Heart Failure | UNKNOWN | NCT00873899 |
| The Medtronic CareLink system (Minneapolis, MN, USA). | Other | Preclinical | Heart Failure | UNKNOWN | NCT00873899 |
| Guidelines 2000 AED protocol | Other | Phase PHASE3 | Heart Arrest | COMPLETED | NCT00139542 |
| One shock per minute AED protocol | Other | Phase PHASE3 | Heart Arrest | COMPLETED | NCT00139542 |
| Guidelines 2000 AED protocol | Other | Phase PHASE3 | Heart Arrest | COMPLETED | NCT00139542 |
| One shock per minute AED protocol | Other | Phase PHASE3 | Heart Arrest | COMPLETED | NCT00139542 |
| rocuronium dose + remifentanil infusion | Other | Approved | Laryngoscopy | UNKNOWN | NCT00926718 |
| remifentanil infusion | Other | Approved | Laryngoscopy | UNKNOWN | NCT00926718 |
| rocuronium dose + remifentanil infusion | Other | Approved | Laryngoscopy | UNKNOWN | NCT00926718 |
| remifentanil infusion | Other | Approved | Laryngoscopy | UNKNOWN | NCT00926718 |
| Gatekeeper Reflux Repair System | Other | Approved | Gastroesophageal Reflux Disease | TERMINATED | NCT00200044 |
| Pump-Assisted Coronary Artery Bypass | Other | Phase PHASE3 | Coronary Artery Bypass Grafting | UNKNOWN | NCT00999089 |
| Off-Pump Coronary Artery Bypass | Other | Phase PHASE3 | Coronary Artery Bypass Grafting | UNKNOWN | NCT00999089 |
| Conventional Coronary Artery Bypass | Other | Phase PHASE3 | Coronary Artery Bypass Grafting | UNKNOWN | NCT00999089 |
| Enterra Therapy | Drug | Approved | Gastroparesis | TERMINATED | NCT00157755 |
| Enterra Therapy | Drug | Approved | Gastroparesis | TERMINATED | NCT00157755 |
| Everolimus eluting stent (Xience - EES) | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00894062 |
| Zotarolimus eluting stent (Endeavor resoulte - ZES resolute) | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00894062 |
| Everolimus eluting stent (Xience - EES) | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00894062 |
| Zotarolimus eluting stent (Endeavor resoulte - ZES resolute) | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00894062 |
| Zotarolimus eluting stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Paclitaxel Eluting Stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Sirolimus Eluting Stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Resolute Sprint | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Zotarolimus eluting stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Paclitaxel Eluting Stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Sirolimus Eluting Stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Resolute Sprint | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Zotarolimus eluting stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Paclitaxel Eluting Stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Sirolimus Eluting Stent | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Resolute Sprint | Other | Phase PHASE4 | Coronary Artery Disease | UNKNOWN | NCT01133925 |
| Implantation of 3-chamber pacemaker | Other | Approved | Right Ventricular Failure | UNKNOWN | NCT01163422 |
| diagnostic electrophysiology catheter | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT01109641 |
| diagnostic electrophysiology catheter | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT01109641 |
| Fluid Status Monitoring (OptiVol™) | Other | Approved | Congestive Heart Failure | COMPLETED | NCT00289276 |
| Fluid Status Monitoring (OptiVol™) | Other | Approved | Congestive Heart Failure | COMPLETED | NCT00289276 |
| CRT pacing | Other | Phase PHASE1 | Mitral Regurgitation | UNKNOWN | NCT01242397 |
| In-Office Care | Other | Approved | Arrhythmia | COMPLETED | NCT00402246 |
| Remote Management | Other | Approved | Arrhythmia | COMPLETED | NCT00402246 |
| In-Office Care | Other | Approved | Arrhythmia | COMPLETED | NCT00402246 |
| Remote Management | Other | Approved | Arrhythmia | COMPLETED | NCT00402246 |
| MiniMed Paradigm REAL-Time System | Other | Phase PHASE4 | Type 1 Diabetes | COMPLETED | NCT00530023 |
| MiniMed Paradigm REAL-Time System | Other | Phase PHASE4 | Type 1 Diabetes | COMPLETED | NCT00530023 |
| Percutaneous Coronary Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00217256 |
| Percutaneous Coronary Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00217256 |
| Open inguinal hernia repair | Other | Approved | Inguinal Hernia | COMPLETED | NCT01026935 |
| Open inguinal hernia repair | Other | Approved | Inguinal Hernia | COMPLETED | NCT01026935 |
| Leads to be implanted according randomization on specified sites. Vitatron pacemakers to be implanted: T60 DR, T70 DR, T20 SR, C60 DR | Other | Phase PHASE4 | Atrioventricular Block | UNKNOWN | NCT00292383 |
| Leads to be implanted according randomization on specified sites. Vitatron pacemakers to be implanted: T60 DR, T70 DR, T20 SR, C60 DR | Other | Phase PHASE4 | Atrioventricular Block | UNKNOWN | NCT00292383 |
| Vitatron T70 DR | Other | Phase PHASE4 | Sick Sinus Syndrome | UNKNOWN | NCT00161551 |
| Vitatron T70 DR | Other | Phase PHASE4 | Sick Sinus Syndrome | UNKNOWN | NCT00161551 |
| Vitatron T70 DR | Other | Phase PHASE4 | Sick Sinus Syndrome | UNKNOWN | NCT00161551 |
| second LV lead in CRT | Other | Phase PHASE4 | Heart Failure | UNKNOWN | NCT01415024 |
| Aventis HOE21PH U400 | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT00211536 |
| Medtronic MiniMed Implantable Pump System | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT00211536 |
| Medtronic MiniMed Implantable Pump Human Recombinant Insulin | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT00211536 |
| Aventis HOE21PH U400 | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT00211536 |
| Medtronic MiniMed Implantable Pump System | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT00211536 |
| Medtronic MiniMed Implantable Pump Human Recombinant Insulin | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT00211536 |
| Occipital Nerve Stimulation | Other | Phase PHASE1 | Chronic Migraine Headache | COMPLETED | NCT00200109 |
| Occipital Nerve Stimulation | Other | Phase PHASE1 | Chronic Migraine Headache | COMPLETED | NCT00200109 |
| Sprinter Legend 1.25mm Balloon Catheter | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00961311 |
| Percutaneous Coronary Intervention | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00961311 |
| Sprinter Legend 1.25mm Balloon Catheter | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00961311 |
| Percutaneous Coronary Intervention | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00961311 |
| Antero-Lateral | Other | Approved | Cardiac Resynchronization Therapy | UNKNOWN | NCT01515761 |
| Postero-lateral | Other | Approved | Cardiac Resynchronization Therapy | UNKNOWN | NCT01515761 |
| Cardiac Resynchronization Therapy (CRT) Device or Implantable Cardioverter Defibrillator (ICD) with CRT | Drug | Approved | Heart Failure | COMPLETED | NCT00271154 |
| Cardiac Resynchronization Therapy (CRT) Device or Implantable Cardioverter Defibrillator (ICD) with CRT | Drug | Approved | Heart Failure | COMPLETED | NCT00271154 |
| EES (Xience) | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01091740 |
| ZES resolute (Endeavor Resolute) | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01091740 |
| There was no intervention. | Other | Preclinical | Epilepsy | COMPLETED | NCT00772421 |
| There was no intervention. | Other | Preclinical | Epilepsy | COMPLETED | NCT00772421 |
| INFUSE® Bone Graft | Other | Preclinical | Alveolar Bone Loss | TERMINATED | NCT00991965 |
| INFUSE® Bone Graft | Other | Preclinical | Alveolar Bone Loss | TERMINATED | NCT00991965 |
| INFUSE® Bone Graft | Other | Preclinical | Alveolar Bone Loss | TERMINATED | NCT00991432 |
| INFUSE® Bone Graft | Other | Preclinical | Alveolar Bone Loss | TERMINATED | NCT00991432 |
| INFUSE® Bone Graft | Other | Preclinical | Alveolar Bone Loss | TERMINATED | NCT00991432 |
| INFUSE® Bone Graft | Other | Preclinical | Maxillary Sinus Bone Loss | TERMINATED | NCT00991393 |
| INFUSE® Bone Graft | Other | Preclinical | Maxillary Sinus Bone Loss | TERMINATED | NCT00991393 |
| INFUSE® Bone Graft | Other | Preclinical | Maxillary Sinus Bone Loss | TERMINATED | NCT00991393 |
| kyphoplasty | Other | Preclinical | Multiple Myeloma | COMPLETED | NCT01006070 |
| kyphoplasty | Other | Preclinical | Multiple Myeloma | COMPLETED | NCT01006070 |
| MARIS-stent (Invatec) | Other | Approved | Peripheral Artery Disease | COMPLETED | NCT01067885 |
| MARIS-stent (Invatec) | Other | Approved | Peripheral Artery Disease | COMPLETED | NCT01067885 |
| Routine in office visits | Other | Approved | Heart Failure | COMPLETED | NCT01045343 |
| Integrated diagnositic system | Other | Approved | Heart Failure | COMPLETED | NCT01045343 |
| Routine in office visits | Other | Approved | Heart Failure | COMPLETED | NCT01045343 |
| Integrated diagnositic system | Other | Approved | Heart Failure | COMPLETED | NCT01045343 |
| Routine in office visits | Other | Approved | Heart Failure | COMPLETED | NCT01045343 |
| Integrated diagnositic system | Other | Approved | Heart Failure | COMPLETED | NCT01045343 |
| Endeavor | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00314275 |
| Coronary Artery Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00314275 |
| Endeavor | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00314275 |
| Coronary Artery Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00314275 |
| Endeavor | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00314275 |
| Coronary Artery Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00314275 |
| Coronary Artery Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00217269 |
| Coronary Artery Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00217269 |
| Coronary Artery Stenting | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00217269 |
| standard electrocautery (Bovie) | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT01583465 |
| Aquamantys | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT01583465 |
| Pressure Support Ventilation | Other | Approved | Respiration, Artificial | TERMINATED | NCT00790725 |
| Proportional Assist Ventilation | Other | Approved | Respiration, Artificial | TERMINATED | NCT00790725 |
| Pressure Support Ventilation | Other | Approved | Respiration, Artificial | TERMINATED | NCT00790725 |
| Proportional Assist Ventilation | Other | Approved | Respiration, Artificial | TERMINATED | NCT00790725 |
| Open inguinal hernia repair with mesh | Other | Preclinical | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | UNKNOWN | NCT01590940 |
| Open inguinal hernia repair with mesh | Other | Preclinical | Evaluate the Use of a New Mesh Type in Open Inguinal Hernia Repair | UNKNOWN | NCT01590940 |
| implantable loop recorder Medtronic reveal XT Full view | Other | Preclinical | Heart Failure | UNKNOWN | NCT01366703 |
| Deep Brain Stimulation System | Other | Phase PHASE2 | Depression | COMPLETED | NCT01069952 |
| deep brain stimulation (ACTIVA PC, Medtronic) | Other | Phase PHASE2 | Parkinson's Disease | COMPLETED | NCT01355835 |
| Endeavor Resolute | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01186094 |
| Cypher | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01186094 |
| Implantable Hemodynamic Monitor (Chronicle® IHM), and IHM in combination with single chamber ICD (Chronicle ICD) | Other | Approved | Heart Failure | COMPLETED | NCT00354159 |
| Implantable Hemodynamic Monitor (Chronicle® IHM), and IHM in combination with single chamber ICD (Chronicle ICD) | Other | Approved | Heart Failure | COMPLETED | NCT00354159 |
| Taxus Liberte | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00418067 |
| Cypher | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00418067 |
| Endeavor | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00418067 |
| Taxus Liberte | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00418067 |
| Cypher | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00418067 |
| Endeavor | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00418067 |
| BIS monitoring | Other | Approved | Gastrointestinal Endoscopy | COMPLETED | NCT00952458 |
| BIS monitoring | Other | Approved | Gastrointestinal Endoscopy | COMPLETED | NCT00952458 |
| Cardiac Resynchronization Therapy | Drug | Phase EARLY_PHASE1 | Heart Failure | COMPLETED | NCT01362465 |
| Medtronic LAA Occlusion Device | Device | Phase PHASE2 | Left Atrial Appendage Occlusion | TERMINATED | NCT00841529 |
| Medtronic LAA Occlusion Device | Device | Phase PHASE2 | Left Atrial Appendage Occlusion | TERMINATED | NCT00841529 |
| Absorbable sutures | Other | Phase PHASE4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | COMPLETED | NCT00223132 |
| Absorbable sutures | Other | Phase PHASE4 | Skin Laxity of Abdomen, Thighs, Chest, Back, and Neck | COMPLETED | NCT00223132 |
| Absorbable Sutures | Other | Phase PHASE4 | Perineal Laceration Repair | TERMINATED | NCT00223119 |
| Absorbable Sutures | Other | Phase PHASE4 | Perineal Laceration Repair | TERMINATED | NCT00223119 |
| Baroreceptor Stimulation | Other | Phase PHASE1 | Hypertension | COMPLETED | NCT01458483 |
| Baroreceptor Stimulation | Other | Phase PHASE1 | Hypertension | COMPLETED | NCT01458483 |
| MMT-7003 subcutaneous glucose sensor | Other | Approved | Diabetes | COMPLETED | NCT00865345 |
| MMT-7003 subcutaneous glucose sensor | Other | Approved | Diabetes | COMPLETED | NCT00865345 |
| Renal Denervation with a catheter-based procedure | Procedure | Phase PHASE1 | Kidney Failure, Chronic | COMPLETED | NCT00753116 |
| Renal Denervation with a catheter-based procedure | Procedure | Phase PHASE1 | Kidney Failure, Chronic | COMPLETED | NCT00753116 |
| Ardian Catheter | Other | Phase PHASE1 | End Stage Renal Disease | COMPLETED | NCT00551304 |
| Ardian Catheter | Other | Phase PHASE1 | End Stage Renal Disease | COMPLETED | NCT00551304 |
| Intensive lifestyle modification and Optimal medical Therapy | Drug | Approved | Type 2 Diabetes | UNKNOWN | NCT01231308 |
| Roux-en-Y-Gastric Bypass | Other | Approved | Type 2 Diabetes | UNKNOWN | NCT01231308 |
| Intensive lifestyle modification and Optimal medical Therapy | Drug | Approved | Type 2 Diabetes | UNKNOWN | NCT01231308 |
| Roux-en-Y-Gastric Bypass | Other | Approved | Type 2 Diabetes | UNKNOWN | NCT01231308 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Macromastia | COMPLETED | NCT00986453 |
| PEAK PlasmaBlade | Other | Approved | Macromastia | COMPLETED | NCT00986453 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Macromastia | COMPLETED | NCT00986453 |
| PEAK PlasmaBlade | Other | Approved | Macromastia | COMPLETED | NCT00986453 |
| Standard of Care (SOC) | Other | Approved | Elastosis | COMPLETED | NCT00943150 |
| PEAK PlasmaBlade | Other | Approved | Elastosis | COMPLETED | NCT00943150 |
| Standard of Care (SOC) | Other | Approved | Elastosis | COMPLETED | NCT00943150 |
| PEAK PlasmaBlade | Other | Approved | Elastosis | COMPLETED | NCT00943150 |
| Scalpel and Traditional Electrosurgery | Procedure | Approved | Macromastia (Symptomatic) | WITHDRAWN | NCT01404351 |
| PEAK PlasmaBlade | Other | Approved | Macromastia (Symptomatic) | WITHDRAWN | NCT01404351 |
| Scalpel and Traditional Electrosurgery | Procedure | Approved | Macromastia (Symptomatic) | WITHDRAWN | NCT01404351 |
| PEAK PlasmaBlade | Other | Approved | Macromastia (Symptomatic) | WITHDRAWN | NCT01404351 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Macromastia | TERMINATED | NCT01284491 |
| PEAK PlasmaBlade 4.0 | Other | Approved | Macromastia | TERMINATED | NCT01284491 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Macromastia | TERMINATED | NCT01284491 |
| PEAK PlasmaBlade 4.0 | Other | Approved | Macromastia | TERMINATED | NCT01284491 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Degenerative Joint Disease | TERMINATED | NCT01081886 |
| PEAK PlasmaBlade 4.0 | Other | Approved | Degenerative Joint Disease | TERMINATED | NCT01081886 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Degenerative Joint Disease | TERMINATED | NCT01081886 |
| PEAK PlasmaBlade 4.0 | Other | Approved | Degenerative Joint Disease | TERMINATED | NCT01081886 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Breast Cancer | TERMINATED | NCT00960154 |
| PEAK PlasmaBlade | Other | Approved | Breast Cancer | TERMINATED | NCT00960154 |
| Traditional Electrosurgery with scalpel | Procedure | Approved | Breast Cancer | TERMINATED | NCT00960154 |
| PEAK PlasmaBlade | Other | Approved | Breast Cancer | TERMINATED | NCT00960154 |
| InterStim Sacral Nerve Stimulation Therapy | Drug | Approved | Fecal Incontinence | COMPLETED | NCT00200057 |
| InterStim Sacral Nerve Stimulation Therapy | Drug | Approved | Fecal Incontinence | COMPLETED | NCT00200057 |
| Medtronic SelectSecure 3830 Lead | Other | Approved | Cardiac Pacing, Artificial | TERMINATED | NCT00422669 |
| Medtronic Dual-Chamber Pacemaker | Other | Approved | Cardiac Pacing, Artificial | TERMINATED | NCT00422669 |
| Medtronic SelectSecure 3830 Lead | Other | Approved | Cardiac Pacing, Artificial | TERMINATED | NCT00422669 |
| Medtronic Dual-Chamber Pacemaker | Other | Approved | Cardiac Pacing, Artificial | TERMINATED | NCT00422669 |
| Medtronic SelectSecure 3830 Lead | Other | Approved | Cardiac Pacing, Artificial | TERMINATED | NCT00422669 |
| Medtronic Dual-Chamber Pacemaker | Other | Approved | Cardiac Pacing, Artificial | TERMINATED | NCT00422669 |
| Zotarolimus-eluting coronary stent | Other | Phase PHASE4 | ST Elevation Myocardial Infarction, Multivessel Coronary Artery Disease | UNKNOWN | NCT01781715 |
| Integrated sensor and infusion set. | Other | Approved | Diabetes Mellitus Type I | UNKNOWN | NCT01775059 |
| Integrated sensor and infusion set. | Other | Approved | Diabetes Mellitus Type I | UNKNOWN | NCT01775059 |
| Integrated sensor and infusion set. | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01773668 |
| Integrated sensor and infusion set. | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01773668 |
| Integrated sensor and infusion set. | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01773668 |
| Integrated sensor and infusion set. | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01773668 |
| Integrated sensor and infusion set. | Other | Approved | Diabetes Type 1 | COMPLETED | NCT01770561 |
| near infrared spectroscopy (INVOS®, Covidien) | Other | Preclinical | Cardiac Arrest | COMPLETED | NCT01531426 |
| near infrared spectroscopy (INVOS®, Covidien) | Other | Preclinical | Cardiac Arrest | COMPLETED | NCT01531426 |
| Medtronic Activa Deep Brain Stimulation | Other | Phase PHASE2 | Obsessive-Compulsive Disorder | COMPLETED | NCT01061983 |
| INFUSE® Bone Graft/PEEK Spacer/Anterior Cervical Plate | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT00485173 |
| INFUSE® Bone Graft/PEEK Spacer/Anterior Cervical Plate | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT00485173 |
| Covidien Triad monopolar generator | Other | Phase PHASE3 | Intraoperative Complications | COMPLETED | NCT01664806 |
| Covidien Triad monopolar generator | Other | Phase PHASE3 | Intraoperative Complications | COMPLETED | NCT01664806 |
| Bispectral Index (BIS) Monitor | Other | Approved | Critical Illness | COMPLETED | NCT00734409 |
| Bispectral Index (BIS) Monitor | Other | Approved | Critical Illness | COMPLETED | NCT00734409 |
| Export Aspiration Catheter, Endeavor resolute or Resolute integrity (Medtronic) | Other | Phase PHASE4 | Acute Myocardial Infarction | UNKNOWN | NCT01156662 |
| Endeavor resolute or Resolute integrity (Medtronic) | Other | Phase PHASE4 | Acute Myocardial Infarction | UNKNOWN | NCT01156662 |
| Enhanced ICD programming | Other | Approved | Cardiac Arrhythmias | UNKNOWN | NCT01715116 |
| 3-0 Monocryl Absorbable Sutures | Other | Approved | Breast Ptosis | COMPLETED | NCT00959374 |
| V-Loc 180/90 Wound Closure Device | Device | Approved | Breast Ptosis | COMPLETED | NCT00959374 |
| 3-0 Monocryl Absorbable Sutures | Other | Approved | Breast Ptosis | COMPLETED | NCT00959374 |
| V-Loc 180/90 Wound Closure Device | Device | Approved | Breast Ptosis | COMPLETED | NCT00959374 |
| Medtronic CapSureFix MRI™ active fixation MRI lead | Other | Approved | Magnetic Resonance Imaging | COMPLETED | NCT01110915 |
| Medtronic Advisa MRI Implantable Pulse Generator (IPG) | Other | Approved | Magnetic Resonance Imaging | COMPLETED | NCT01110915 |
| Medtronic CapSureFix MRI™ active fixation MRI lead | Other | Approved | Magnetic Resonance Imaging | COMPLETED | NCT01110915 |
| Medtronic Advisa MRI Implantable Pulse Generator (IPG) | Other | Approved | Magnetic Resonance Imaging | COMPLETED | NCT01110915 |
| Medtronic CapSureFix MRI™ active fixation MRI lead | Other | Approved | Magnetic Resonance Imaging | COMPLETED | NCT01110915 |
| Medtronic Advisa MRI Implantable Pulse Generator (IPG) | Other | Approved | Magnetic Resonance Imaging | COMPLETED | NCT01110915 |
| Quarterly Review Arm | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT00847288 |
| Monthly Review Arm | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT00847288 |
| Quarterly Review Arm | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT00847288 |
| Monthly Review Arm | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT00847288 |
| InterStim Therapy | Drug | Approved | Urgency Frequency | COMPLETED | NCT01009333 |
| InterStim Therapy at rate 14 Hz | Drug | Approved | Urgency Frequency | COMPLETED | NCT01009333 |
| InterStim Therapy at rate 5.2 Hz | Drug | Approved | Urgency Frequency | COMPLETED | NCT01009333 |
| InterStim Therapy | Drug | Approved | Urgency Frequency | COMPLETED | NCT01009333 |
| InterStim Therapy at rate 14 Hz | Drug | Approved | Urgency Frequency | COMPLETED | NCT01009333 |
| InterStim Therapy at rate 5.2 Hz | Drug | Approved | Urgency Frequency | COMPLETED | NCT01009333 |
| CRyo-Ablation to Treat HOCM. | Other | Approved | HOCM, Hypertrophic Obstructive Cardiomyopathy | UNKNOWN | NCT01875016 |
| Conventional cardiac resynchronization | Other | Phase PHASE3 | Heart Failure | COMPLETED | NCT00887237 |
| CRT with triple site ventricular stimulation | Other | Phase PHASE3 | Heart Failure | COMPLETED | NCT00887237 |
| Conventional cardiac resynchronization | Other | Phase PHASE3 | Heart Failure | COMPLETED | NCT00887237 |
| CRT with triple site ventricular stimulation | Other | Phase PHASE3 | Heart Failure | COMPLETED | NCT00887237 |
| Defibrillation testing | Other | Phase PHASE4 | Ventricular Arrhythmias | UNKNOWN | NCT01905007 |
| Cryoballoon ablation. | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT01448265 |
| Autogenous bone/CORNERSTONE-SR™ /ATLANTIS™ | Other | Approved | Degenerative Cervical Disc Disease | TERMINATED | NCT01491477 |
| INFUSE™ Bone Graft/CORNERSTONE-SR™ /ATLANTIS™ | Other | Approved | Degenerative Cervical Disc Disease | TERMINATED | NCT01491477 |
| Autogenous bone/CORNERSTONE-SR™ /ATLANTIS™ | Other | Approved | Degenerative Cervical Disc Disease | TERMINATED | NCT01491477 |
| INFUSE™ Bone Graft/CORNERSTONE-SR™ /ATLANTIS™ | Other | Approved | Degenerative Cervical Disc Disease | TERMINATED | NCT01491477 |
| LT-CAGE® Lumbar Tapered Fusion Device and INFUSE® Bone Graft | Device | Phase PHASE3 | Spinal Diseases | COMPLETED | NCT00635843 |
| MAVERICK™ Disc | Other | Phase PHASE3 | Spinal Diseases | COMPLETED | NCT00635843 |
| LT-CAGE® Lumbar Tapered Fusion Device and INFUSE® Bone Graft | Device | Phase PHASE3 | Spinal Diseases | COMPLETED | NCT00635843 |
| MAVERICK™ Disc | Other | Phase PHASE3 | Spinal Diseases | COMPLETED | NCT00635843 |
| InSync III Model 8042 | Other | Preclinical | Heart Failure | COMPLETED | NCT00273182 |
| InSync Model 8040 | Other | Preclinical | Heart Failure | COMPLETED | NCT00273182 |
| InSync III Model 8042 | Other | Preclinical | Heart Failure | COMPLETED | NCT00273182 |
| InSync Model 8040 | Other | Preclinical | Heart Failure | COMPLETED | NCT00273182 |
| Duet TRS | Other | Approved | Lung Cancer | WITHDRAWN | NCT01026025 |
| Duet TRS | Other | Approved | Lung Cancer | WITHDRAWN | NCT01026025 |
| Intraspinal Gabapentin | Other | Phase PHASE2 | Chronic Intractable Pain | TERMINATED | NCT00414466 |
| Intraspinal Gabapentin | Other | Phase PHASE2 | Chronic Intractable Pain | TERMINATED | NCT00414466 |
| Same-day discharge | Other | Phase PHASE4 | Acute Coronary Syndrome | TERMINATED | NCT01068119 |
| stent placement | Other | Phase PHASE4 | Peripheral Arterial Disease | COMPLETED | NCT01412463 |
| stent placement | Other | Phase PHASE4 | Peripheral Arterial Disease | COMPLETED | NCT01412463 |
| Breathing Exercise Cohort | Other | Approved | Unexplained Syncope | UNKNOWN | NCT01956578 |
| Breathing Exercise Cohort | Other | Approved | Unexplained Syncope | UNKNOWN | NCT01956578 |
| Drug eluting stent | Drug | Approved | Coronary Artery Disease | COMPLETED | NCT01956448 |
| Drug eluting stent | Drug | Approved | Coronary Artery Disease | COMPLETED | NCT01956448 |
| Sham Stimulation | Other | Phase PHASE1 | Inflammation | COMPLETED | NCT01944228 |
| Vagal Nerve Stimulation | Other | Phase PHASE1 | Inflammation | COMPLETED | NCT01944228 |
| Sham Stimulation | Other | Phase PHASE1 | Inflammation | COMPLETED | NCT01944228 |
| Vagal Nerve Stimulation | Other | Phase PHASE1 | Inflammation | COMPLETED | NCT01944228 |
| Symplicty(TM) Catheter System | Other | Approved | Hypertension | COMPLETED | NCT00664638 |
| Symplicty(TM) Catheter System | Other | Approved | Hypertension | COMPLETED | NCT00664638 |
| Minimally invasive coronary artery bypass graft surgery | Procedure | Phase PHASE4 | Arteriosclerosis of Coronary Artery Bypass Graft | COMPLETED | NCT01334866 |
| Minimally invasive coronary artery bypass graft surgery | Procedure | Phase PHASE4 | Arteriosclerosis of Coronary Artery Bypass Graft | COMPLETED | NCT01334866 |
| Surgical RF Ablation | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00431834 |
| Cardioblate System Surgical Ablation System | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00431834 |
| Surgical RF Ablation | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00431834 |
| Cardioblate System Surgical Ablation System | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00431834 |
| Transradial intervention | Other | Approved | Transradial-transfemoral Coronary Interventions Comparison | WITHDRAWN | NCT01735110 |
| transfemoral intervention (TFI) | Other | Approved | Transradial-transfemoral Coronary Interventions Comparison | WITHDRAWN | NCT01735110 |
| LV stimulus intensity | Other | Approved | Congestive Heart Failure | COMPLETED | NCT01060449 |
| Type: Implantable neurostimulator; InterStim | Other | Phase PHASE4 | Fecal Incontinence and Constipation | COMPLETED | NCT00200005 |
| Type: Implantable neurostimulator; InterStim | Other | Phase PHASE4 | Fecal Incontinence and Constipation | COMPLETED | NCT00200005 |
| Itrel II™ and Soletra™ Epilepsy Control System | Other | Preclinical | Epilepsy | COMPLETED | NCT00736424 |
| Itrel II™ and Soletra™ Epilepsy Control System | Other | Preclinical | Epilepsy | COMPLETED | NCT00736424 |
| Education | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01223547 |
| systemic and cerebral oxymetry | Other | Preclinical | Cerebral Desaturation | COMPLETED | NCT01458262 |
| systemic and cerebral oxymetry | Other | Preclinical | Cerebral Desaturation | COMPLETED | NCT01458262 |
| AVNS ON | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01095952 |
| AVNS ON | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01095952 |
| AVNS ON | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01095952 |
| Facilitate nerve stimulation lead placement with the nerve access tool | Other | Approved | Cystocele | WITHDRAWN | NCT00942474 |
| Facilitate nerve stimulation lead placement with the nerve access tool | Other | Approved | Cystocele | WITHDRAWN | NCT00942474 |
| Facilitate nerve stimulation lead placement with the nerve access tool | Other | Approved | Cystocele | WITHDRAWN | NCT00942474 |
| Veriset™ Hemostatic Patch | Other | Approved | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | COMPLETED | NCT01719172 |
| Veriset™ Hemostatic Patch | Other | Approved | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | COMPLETED | NCT01719172 |
| Veriset™ Hemostatic Patch | Other | Approved | Non-emergent, Soft Tissue Procedures, Performed Via an Open Approach | COMPLETED | NCT01719172 |
| Fibrin Sealant (TachoSil®) | Other | Approved | Liver Disease | COMPLETED | NCT01324349 |
| Veriset Hemostatic Patch | Other | Approved | Liver Disease | COMPLETED | NCT01324349 |
| Fibrin Sealant (TachoSil®) | Other | Approved | Liver Disease | COMPLETED | NCT01324349 |
| Veriset Hemostatic Patch | Other | Approved | Liver Disease | COMPLETED | NCT01324349 |
| Fibrin Sealant (TachoSil®) | Other | Approved | Liver Disease | COMPLETED | NCT01324349 |
| Veriset Hemostatic Patch | Other | Approved | Liver Disease | COMPLETED | NCT01324349 |
| Tri Staple Technology stapler | Other | Approved | Sleep Apnea | COMPLETED | NCT01026103 |
| Tri Staple Technology stapler | Other | Approved | Sleep Apnea | COMPLETED | NCT01026103 |
| Medtronic (NO LGS FEATURE ) using Paradigm® Revel™2.0 Pump | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT01497938 |
| Medtronic MMT-754 Veo Insulin pump testing Low Glucose Suspend (LGS) feature | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT01497938 |
| Medtronic (NO LGS FEATURE ) using Paradigm® Revel™2.0 Pump | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT01497938 |
| Medtronic MMT-754 Veo Insulin pump testing Low Glucose Suspend (LGS) feature | Other | Phase PHASE3 | Type 1 Diabetes | COMPLETED | NCT01497938 |
| Marcaine | Other | Phase PHASE4 | Pain | COMPLETED | NCT01308554 |
| Placebo: sterile normal saline | Other | Phase PHASE4 | Pain | COMPLETED | NCT01308554 |
| Marcaine | Other | Phase PHASE4 | Pain | COMPLETED | NCT01308554 |
| Placebo: sterile normal saline | Other | Phase PHASE4 | Pain | COMPLETED | NCT01308554 |
| Cardiac Resynchronization Therapy (CRT) | Drug | Approved | Atrioventricular Block | COMPLETED | NCT00267098 |
| Cardiac Resynchronization Therapy (CRT) | Drug | Approved | Atrioventricular Block | COMPLETED | NCT00267098 |
| Cardiac Resynchronization Therapy (CRT) | Drug | Approved | Atrioventricular Block | COMPLETED | NCT00267098 |
| Duet TRS | Other | Approved | Roux En Y Gastric Bypass | COMPLETED | NCT00950872 |
| Duet TRS | Other | Approved | Roux En Y Gastric Bypass | COMPLETED | NCT00950872 |
| Use of continuous glucose monitor during surgery. ( Medtronic Minimed Guardian REALTime Continuous Glucose Monitor) | Procedure | Preclinical | Cardiac Surgery | WITHDRAWN | NCT01394588 |
| Permacol Surgical Implant | Other | Preclinical | Abdominal Wall Defects | COMPLETED | NCT01214252 |
| Permacol Surgical Implant | Other | Preclinical | Abdominal Wall Defects | COMPLETED | NCT01214252 |
| Sotalol | Other | Phase PHASE4 | Atrial Fibrillation | UNKNOWN | NCT02145546 |
| Propafenone | Other | Phase PHASE4 | Atrial Fibrillation | UNKNOWN | NCT02145546 |
| Amiodarone | Other | Phase PHASE4 | Atrial Fibrillation | UNKNOWN | NCT02145546 |
| Sotalol | Other | Phase PHASE4 | Atrial Fibrillation | UNKNOWN | NCT02145546 |
| Propafenone | Other | Phase PHASE4 | Atrial Fibrillation | UNKNOWN | NCT02145546 |
| Amiodarone | Other | Phase PHASE4 | Atrial Fibrillation | UNKNOWN | NCT02145546 |
| Medtronic 4195 active fixation LV lead and Medtronic passive fixation LV lead | Other | Approved | Congestive Heart Failure | TERMINATED | NCT01520714 |
| Abbott Xience V | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00617084 |
| Medtronic Endeavor Resolute | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00617084 |
| Abbott Xience V | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00617084 |
| Medtronic Endeavor Resolute | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT00617084 |
| Pennsaid | Other | Phase PHASE3 | Osteoarthritis of the Knee | COMPLETED | NCT01511939 |
| Pennsaid | Other | Phase PHASE3 | Osteoarthritis of the Knee | COMPLETED | NCT01511939 |
| TachoSil® | Other | Approved | Cardiac Surgical Procedures | COMPLETED | NCT01639833 |
| Veriset Hemostatic Patch | Other | Approved | Cardiac Surgical Procedures | COMPLETED | NCT01639833 |
| TachoSil® | Other | Approved | Cardiac Surgical Procedures | COMPLETED | NCT01639833 |
| Veriset Hemostatic Patch | Other | Approved | Cardiac Surgical Procedures | COMPLETED | NCT01639833 |
| TachoSil® | Other | Approved | Cardiac Surgical Procedures | COMPLETED | NCT01639833 |
| Veriset Hemostatic Patch | Other | Approved | Cardiac Surgical Procedures | COMPLETED | NCT01639833 |
| ENDO GIA™ Stapler with TRI-STAPLE™ Technology | Other | Approved | Lung Cancer | COMPLETED | NCT01241565 |
| ENDO GIA™ Stapler with TRI-STAPLE™ Technology | Other | Approved | Lung Cancer | COMPLETED | NCT01241565 |
| Medtronic INTERSIM II - 3058 | Other | Approved | Fecal Incontinence | TERMINATED | NCT00913601 |
| Medtronic INTERSIM II - 3058 | Other | Approved | Fecal Incontinence | TERMINATED | NCT00913601 |
| Medtronic INTERSIM II - 3058 | Other | Approved | Fecal Incontinence | TERMINATED | NCT00913601 |
| Therapy Programming Report (TPR) | Drug | Preclinical | Cardiovascular Disease | COMPLETED | NCT00856349 |
| Therapy Programming Report (TPR) | Drug | Preclinical | Cardiovascular Disease | COMPLETED | NCT00856349 |
| Akern BIA101 and Custom Device | Device | Phase PHASE1 | Heart Failure | TERMINATED | NCT01509495 |
| Akern BIA101 and Custom Device | Device | Phase PHASE1 | Heart Failure | TERMINATED | NCT01509495 |
| Bilateral Deep Brain Stimulation | Other | Phase PHASE3 | Parkinson's Disease | COMPLETED | NCT01076452 |
| Reveal® XT Insertable Cardiac Monitor | Other | Phase PHASE4 | Cryptogenic Symptomatic Transient Ischemic Attack | COMPLETED | NCT00924638 |
| Reveal® XT Insertable Cardiac Monitor | Other | Phase PHASE4 | Cryptogenic Symptomatic Transient Ischemic Attack | COMPLETED | NCT00924638 |
| Reveal® XT Insertable Cardiac Monitor | Other | Phase PHASE4 | Cryptogenic Symptomatic Transient Ischemic Attack | COMPLETED | NCT00924638 |
| Oxygen Monitoring | Other | Preclinical | Sleep Disordered Breathing | COMPLETED | NCT01082575 |
| Oxygen Monitoring | Other | Preclinical | Sleep Disordered Breathing | COMPLETED | NCT01082575 |
| conventional laparoscopic appendectomy | Other | Approved | Appendicitis | TERMINATED | NCT00997516 |
| SILS appendectomy | Other | Approved | Appendicitis | TERMINATED | NCT00997516 |
| conventional laparoscopic appendectomy | Other | Approved | Appendicitis | TERMINATED | NCT00997516 |
| SILS appendectomy | Other | Approved | Appendicitis | TERMINATED | NCT00997516 |
| duodenal exclusion | Other | Phase PHASE4 | Diabetes | COMPLETED | NCT00456352 |
| duodenal exclusion | Other | Phase PHASE4 | Diabetes | COMPLETED | NCT00456352 |
| duodenal exclusion | Other | Phase PHASE4 | Diabetes | COMPLETED | NCT00456352 |
| ileal interposition with a sleeve gastrectomy | Other | Phase PHASE4 | Diabetes | COMPLETED | NCT00450710 |
| ileal interposition with a sleeve gastrectomy | Other | Phase PHASE4 | Diabetes | COMPLETED | NCT00450710 |
| ileal interposition with a sleeve gastrectomy | Other | Phase PHASE4 | Diabetes | COMPLETED | NCT00450710 |
| Evaluation of propofol effect | Other | Phase PHASE4 | Healthy | COMPLETED | NCT02155517 |
| Evaluation of propofol effect | Other | Phase PHASE4 | Healthy | COMPLETED | NCT02155517 |
| Zotarolimus eluting stent | Other | Phase PHASE4 | Myocardial Infarction | COMPLETED | NCT01347554 |
| Everolimus eluting stent | Other | Phase PHASE4 | Myocardial Infarction | COMPLETED | NCT01347554 |
| Hemorrhoidopexy | Other | Approved | Hemorrhoid | COMPLETED | NCT01169311 |
| Hemorrhoidopexy | Other | Approved | Hemorrhoid | COMPLETED | NCT01169311 |
| Renal denervation device | Device | Approved | Treatment-Resistant Hypertension | TERMINATED | NCT01895140 |
| Endosurgery Proximate PPH03 Stapling Set | Procedure | Approved | Hemorrhoids | COMPLETED | NCT01306877 |
| EEA Hemorrhoid and Prolapse Stapling Set | Other | Approved | Hemorrhoids | COMPLETED | NCT01306877 |
| Endosurgery Proximate PPH03 Stapling Set | Procedure | Approved | Hemorrhoids | COMPLETED | NCT01306877 |
| EEA Hemorrhoid and Prolapse Stapling Set | Other | Approved | Hemorrhoids | COMPLETED | NCT01306877 |
| Ultrasound (Trademark:VScan; Manufacturer:General Electric) | Other | Phase EARLY_PHASE1 | Abdominal Aortic Aneurysm | COMPLETED | NCT01882634 |
| Stent | Other | Phase PHASE4 | Ischemic Heart Disease | COMPLETED | NCT00476957 |
| Stent | Other | Phase PHASE4 | Ischemic Heart Disease | COMPLETED | NCT00476957 |
| Stent | Other | Phase PHASE4 | Ischemic Heart Disease | COMPLETED | NCT00476957 |
| Surgical Treatment | Drug | Phase PHASE4 | Diabetes | WITHDRAWN | NCT00596973 |
| Surgical Treatment | Drug | Phase PHASE4 | Diabetes | WITHDRAWN | NCT00596973 |
| Surgical Treatment | Drug | Phase PHASE4 | Diabetes | WITHDRAWN | NCT00596973 |
| Adalimumab | Other | Phase PHASE4 | Spondyloarthritis | COMPLETED | NCT01174186 |
| Adalimumab | Other | Phase PHASE4 | Spondyloarthritis | COMPLETED | NCT01174186 |
| Capsule endoscopy | Other | Phase EARLY_PHASE1 | Lynch Syndrome | COMPLETED | NCT00898768 |
| Multiple daily insulin injections (MDI) | Other | Phase PHASE4 | Type 1 Diabetes Mellitus | COMPLETED | NCT01454700 |
| Insulin pump therapy (CSII) plus continuous glucose monitoring (CGM) | Drug | Phase PHASE4 | Type 1 Diabetes Mellitus | COMPLETED | NCT01454700 |
| Pipeline Embolization Device | Device | Preclinical | Brain Aneurysm | TERMINATED | NCT01557036 |
| Pipeline Embolization Device | Device | Preclinical | Brain Aneurysm | TERMINATED | NCT01557036 |
| Endeavor Zotarolimus-Eluting Coronary Stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00609947 |
| Endeavor Zotarolimus-Eluting Coronary Stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT00609947 |
| Covidien Radial Reload Stapler with Tri-Staple Technology | Other | Approved | Low Anterior Resection | TERMINATED | NCT01717014 |
| Covidien Radial Reload Stapler with Tri-Staple Technology | Other | Approved | Low Anterior Resection | TERMINATED | NCT01717014 |
| Activa RC | Other | Phase PHASE4 | Parkinson's Disease | COMPLETED | NCT00998660 |
| Implantable Cardioverter-Defibrillator (subject's pre-existing ICD) | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT01446796 |
| Covidien Radial Reload Stapler with Tri-Staple Technology | Other | Phase PHASE4 | Colorectal Cancer | TERMINATED | NCT01706822 |
| Covidien Radial Reload Stapler with Tri-Staple Technology | Other | Phase PHASE4 | Colorectal Cancer | TERMINATED | NCT01706822 |
| Endovascular thrombectomy/thrombolysis | Other | Phase PHASE3 | Ischemic Stroke | TERMINATED | NCT01778335 |
| Endovascular thrombectomy/thrombolysis | Other | Phase PHASE3 | Ischemic Stroke | TERMINATED | NCT01778335 |
| Gelfoam/Thrombin | Other | Phase PHASE1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | TERMINATED | NCT00618358 |
| Vascular Sealant System | Other | Phase PHASE1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | TERMINATED | NCT00618358 |
| Gelfoam/Thrombin | Other | Phase PHASE1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | TERMINATED | NCT00618358 |
| Vascular Sealant System | Other | Phase PHASE1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | TERMINATED | NCT00618358 |
| Gelfoam/Thrombin | Other | Phase PHASE1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | TERMINATED | NCT00618358 |
| Vascular Sealant System | Other | Phase PHASE1 | Arteriovenous Access Grafts or Extra-anatomic and Infra-inguinal Grafts | TERMINATED | NCT00618358 |
| Placement of interstim lead | Other | Approved | Urinary Incontinence | TERMINATED | NCT01054534 |
| Roux-en-Y gastric bypass surgery | Procedure | Approved | Obesity | COMPLETED | NCT01044602 |
| Best Medical Management | Other | Approved | Obesity | COMPLETED | NCT01044602 |
| Laboratory evaluations, sleep study | Other | Approved | Obesity | COMPLETED | NCT01044602 |
| Roux-en-Y gastric bypass surgery | Procedure | Approved | Obesity | COMPLETED | NCT01044602 |
| Best Medical Management | Other | Approved | Obesity | COMPLETED | NCT01044602 |
| Laboratory evaluations, sleep study | Other | Approved | Obesity | COMPLETED | NCT01044602 |
| Endeavor® Zotarolimus Eluting Coronary Stent System | Other | Phase PHASE4 | Coronary Artery Disease, Autosomal Dominant, 1 | COMPLETED | NCT00846846 |
| Endeavor® Zotarolimus Eluting Coronary Stent System | Other | Phase PHASE4 | Coronary Artery Disease, Autosomal Dominant, 1 | COMPLETED | NCT00846846 |
| MDT-4107 Drug Eluting Stent | Drug | Approved | Arterial Occlusive Diseases | COMPLETED | NCT00927940 |
| MDT-4107 Drug Eluting Stent | Drug | Approved | Arterial Occlusive Diseases | COMPLETED | NCT00927940 |
| Reclaim™ DBS System | Other | Phase PHASE2 | Depression | COMPLETED | NCT00837486 |
| Reclaim™ DBS System | Other | Phase PHASE2 | Depression | COMPLETED | NCT00837486 |
| 46 hrs Holter ECG recording | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00680927 |
| 46 hrs Holter ECG recording | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00680927 |
| Tack fixation | Other | Approved | Inguinal Hernia | UNKNOWN | NCT02467140 |
| Parietex ProGrib self-fixating mesh | Other | Approved | Inguinal Hernia | UNKNOWN | NCT02467140 |
| Tack fixation | Other | Approved | Inguinal Hernia | UNKNOWN | NCT02467140 |
| Parietex ProGrib self-fixating mesh | Other | Approved | Inguinal Hernia | UNKNOWN | NCT02467140 |
| Capsule endoscopy (PillCam ESO) with abdominal binder | Other | Phase PHASE3 | Esophageal Varices | WITHDRAWN | NCT00911131 |
| EGD | Other | Phase PHASE3 | Esophageal Varices | WITHDRAWN | NCT00911131 |
| Capsule endoscopy (PillCam ESO) | Other | Phase PHASE3 | Esophageal Varices | WITHDRAWN | NCT00911131 |
| Capsule endoscopy (PillCam ESO) with abdominal binder | Other | Phase PHASE3 | Esophageal Varices | WITHDRAWN | NCT00911131 |
| EGD | Other | Phase PHASE3 | Esophageal Varices | WITHDRAWN | NCT00911131 |
| Capsule endoscopy (PillCam ESO) | Other | Phase PHASE3 | Esophageal Varices | WITHDRAWN | NCT00911131 |
| Activated clotting time versus blood-heparin concentration | Other | Approved | Cardiac Surgery | WITHDRAWN | NCT01462968 |
| ILR implantation | Other | Phase PHASE2 | Myocardial Infarction | COMPLETED | NCT02492243 |
| PCI | Other | Phase PHASE2 | Myocardial Infarction | COMPLETED | NCT02492243 |
| ILR implantation | Other | Phase PHASE2 | Myocardial Infarction | COMPLETED | NCT02492243 |
| PCI | Other | Phase PHASE2 | Myocardial Infarction | COMPLETED | NCT02492243 |
| ILR implantation | Other | Phase PHASE2 | Myocardial Infarction | COMPLETED | NCT02492243 |
| PCI | Other | Phase PHASE2 | Myocardial Infarction | COMPLETED | NCT02492243 |
| Therapy Setting 4 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 3 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 2 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 1 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 4 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 3 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 2 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 1 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 4 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 3 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 2 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Therapy Setting 1 (Medtronic) | Drug | Approved | Failed Back Surgery Syndrome | WITHDRAWN | NCT02371122 |
| Epicardial implantation of cardiac resynchronization therapy device | Drug | Phase PHASE3 | Ischemic Heart Failure | COMPLETED | NCT00846001 |
| Coronary artery bypass grafting | Other | Phase PHASE3 | Ischemic Heart Failure | COMPLETED | NCT00846001 |
| Epicardial implantation of cardiac resynchronization therapy device | Drug | Phase PHASE3 | Ischemic Heart Failure | COMPLETED | NCT00846001 |
| Coronary artery bypass grafting | Other | Phase PHASE3 | Ischemic Heart Failure | COMPLETED | NCT00846001 |
| No stimulation | Other | Phase PHASE1 | Major Depressive Disorder | TERMINATED | NCT01921543 |
| CI/BNST stimulation | Other | Phase PHASE1 | Major Depressive Disorder | TERMINATED | NCT01921543 |
| ITP Stimulation | Other | Phase PHASE1 | Major Depressive Disorder | TERMINATED | NCT01921543 |
| Pacemaker System | Other | Approved | Magnetic Resonance Imaging (MRI) | COMPLETED | NCT01755143 |
| Magnetic Resonance Imaging scan sequences of the head, neck, and chest | Other | Approved | Magnetic Resonance Imaging (MRI) | COMPLETED | NCT01755143 |
| Pacemaker System | Other | Approved | Magnetic Resonance Imaging (MRI) | COMPLETED | NCT01755143 |
| Magnetic Resonance Imaging scan sequences of the head, neck, and chest | Other | Approved | Magnetic Resonance Imaging (MRI) | COMPLETED | NCT01755143 |
| Duodenal Exclusion | Other | Approved | Diabetes | WITHDRAWN | NCT00534547 |
| Duodenal Exclusion | Other | Approved | Diabetes | WITHDRAWN | NCT00534547 |
| Duodenal Exclusion | Other | Approved | Diabetes | WITHDRAWN | NCT00534547 |
| LigaSure Force Triad Vessel Sealing System | Other | Phase PHASE3 | Lung Resection | TERMINATED | NCT01349426 |
| LigaSure Force Triad Vessel Sealing System | Other | Phase PHASE3 | Lung Resection | TERMINATED | NCT01349426 |
| Adhesive and non-adhesive oximetry sensors | Other | Preclinical | Premature Birth | TERMINATED | NCT00179972 |
| Adhesive and non-adhesive oximetry sensors | Other | Preclinical | Premature Birth | TERMINATED | NCT00179972 |
| ATS Medical 3f® Aortic Bioprosthesis, Model 1000 19mm | Other | Preclinical | Heart Valve Diseases | WITHDRAWN | NCT01156272 |
| Optical coherence tomography | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02060357 |
| Collection of measurements during LV pacing during electrophysiology study | Other | Approved | Cardiomyopathy | WITHDRAWN | NCT01825239 |
| Methylene Blue | Other | Approved | Respiratory Aspiration | COMPLETED | NCT01539135 |
| Methylene Blue | Other | Approved | Respiratory Aspiration | COMPLETED | NCT01539135 |
| Renal Denervation (OneShot™ Renal Denervation System) | Other | Phase PHASE2 | Resistant Hypertension | WITHDRAWN | NCT01939392 |
| Renal Denervation (OneShot™ Renal Denervation System) | Other | Phase PHASE2 | Resistant Hypertension | WITHDRAWN | NCT01939392 |
| OneShot Ablation System | Other | Phase PHASE2 | Hypertension | TERMINATED | NCT01844037 |
| OneShot Ablation System | Other | Phase PHASE2 | Hypertension | TERMINATED | NCT01844037 |
| Echocardiography-guided approach | Other | Approved | Heart Failure | WITHDRAWN | NCT01014000 |
| Empirical group | Other | Approved | Heart Failure | WITHDRAWN | NCT01014000 |
| CD HORIZON BalanC™ Medtronic | Other | Approved | Spine Surgery | UNKNOWN | NCT02551302 |
| Solera™ Medtronic | Other | Approved | Spine Surgery | UNKNOWN | NCT02551302 |
| ProTack | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00749268 |
| AbsorbaTack | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00749268 |
| ProTack | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00749268 |
| AbsorbaTack | Other | Phase PHASE4 | Hernia, Inguinal | COMPLETED | NCT00749268 |
| OCT | Other | Approved | Coronary Disease | UNKNOWN | NCT02234804 |
| Angiography | Other | Approved | Coronary Disease | UNKNOWN | NCT02234804 |
| Medtronic Resolute Integrity stent | Other | Approved | Coronary Disease | UNKNOWN | NCT02234804 |
| Xience Prime Stent | Other | Approved | Coronary Disease | UNKNOWN | NCT02234804 |
| remote patient's management | Other | Preclinical | Heart Failure | COMPLETED | NCT01216670 |
| remote patient's management | Other | Preclinical | Heart Failure | COMPLETED | NCT01216670 |
| remote patient's management | Other | Preclinical | Heart Failure | COMPLETED | NCT01216670 |
| Bispectral index monitor | Other | Phase PHASE4 | Brain Injury | TERMINATED | NCT00538369 |
| Ramsay Scale | Other | Phase PHASE4 | Brain Injury | TERMINATED | NCT00538369 |
| Bispectral index monitor | Other | Phase PHASE4 | Brain Injury | TERMINATED | NCT00538369 |
| Ramsay Scale | Other | Phase PHASE4 | Brain Injury | TERMINATED | NCT00538369 |
| Medtronic PrimeADVANCED Neurostimulator | Other | Phase PHASE2 | Heart Failure | COMPLETED | NCT01112579 |
| Medtronic PrimeADVANCED Neurostimulator | Other | Phase PHASE2 | Heart Failure | COMPLETED | NCT01112579 |
| CG Future Annuloplasty Ring/Band | Other | Phase PHASE4 | Mitral Valve Insufficiency | COMPLETED | NCT01074671 |
| CG Future Annuloplasty Ring/Band | Other | Phase PHASE4 | Mitral Valve Insufficiency | COMPLETED | NCT01074671 |
| Aortic implantation of Mosaic Ultra porcine bioprosthesis | Other | Preclinical | Aortic Valve Replacement | COMPLETED | NCT00477555 |
| Aortic implantation of Mosaic Ultra porcine bioprosthesis | Other | Preclinical | Aortic Valve Replacement | COMPLETED | NCT00477555 |
| Valve replacement | Other | Preclinical | Aortic Heart Valve Diseases | COMPLETED | NCT01213615 |
| Valve replacement | Other | Preclinical | Aortic Heart Valve Diseases | COMPLETED | NCT01213615 |
| CARB counting | Other | Phase PHASE4 | Type 1 Diabetes Mellitus | COMPLETED | NCT01400659 |
| CFP counting | Other | Phase PHASE4 | Type 1 Diabetes Mellitus | COMPLETED | NCT01400659 |
| Clopidogrel | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01113372 |
| Medtronic Reveal XT implantable loop recorder | Other | Phase PHASE4 | Atrial Fibrillation | UNKNOWN | NCT01461434 |
| 3D high resolution anorectal manometry | Other | Approved | Children | COMPLETED | NCT02236507 |
| 3D high resolution anorectal manometry | Other | Approved | Children | COMPLETED | NCT02236507 |
| 3D high resolution anorectal manometry | Other | Approved | Children | COMPLETED | NCT02236507 |
| Clopidogrel | Other | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01325935 |
| sNN0029 | Other | Phase PHASE1 | Amyotrophic Lateral Sclerosis | TERMINATED | NCT01384162 |
| lumbar spinal arthroplasty + Maverick™ | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT01338493 |
| lumbar spinal arthroplasty + Maverick™ | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT01338493 |
| Aperius® Percutaneous Interspinous Spacer | Other | Phase PHASE4 | Spinal Stenosis | COMPLETED | NCT00887744 |
| Aperius® Percutaneous Interspinous Spacer | Other | Phase PHASE4 | Spinal Stenosis | COMPLETED | NCT00887744 |
| Aperius® Percutaneous Interspinous Spacer | Other | Phase PHASE4 | Spinal Stenosis | COMPLETED | NCT00887744 |
| Herniectomy | Other | Phase PHASE4 | Sciatica | COMPLETED | NCT00749996 |
| DIAM™ Spinal Stabilization System | Other | Phase PHASE4 | Sciatica | COMPLETED | NCT00749996 |
| Herniectomy | Other | Phase PHASE4 | Sciatica | COMPLETED | NCT00749996 |
| DIAM™ Spinal Stabilization System | Other | Phase PHASE4 | Sciatica | COMPLETED | NCT00749996 |
| Symplicity Renal Denervation | Other | Phase PHASE2 | Heart Failure | TERMINATED | NCT01954160 |
| RapidVac Smoke Evacuator | Other | Approved | Smoke | UNKNOWN | NCT02672969 |
| RapidVac Smoke Evacuator | Other | Approved | Smoke | UNKNOWN | NCT02672969 |
| RapidVac Smoke Evacuator | Other | Approved | Smoke | UNKNOWN | NCT02672969 |
| Medical treatment | Drug | Phase PHASE3 | Acute Stroke | TERMINATED | NCT01692379 |
| Solitaire FR device | Device | Phase PHASE3 | Acute Stroke | TERMINATED | NCT01692379 |
| Medical treatment | Drug | Phase PHASE3 | Acute Stroke | TERMINATED | NCT01692379 |
| Solitaire FR device | Device | Phase PHASE3 | Acute Stroke | TERMINATED | NCT01692379 |
| Radiofrequency Ablation (HALO Ablation Systems) | Other | Approved | Barrett Esophagus | COMPLETED | NCT00848237 |
| Radiofrequency Ablation (HALO Ablation Systems) | Other | Approved | Barrett Esophagus | COMPLETED | NCT00848237 |
| Medtronic Restore Advanced 37713 | Other | Approved | Obsessive-compulsive Disorder | COMPLETED | NCT02685280 |
| Activa PC+S | Other | Approved | Parkinson's Disease | UNKNOWN | NCT02115802 |
| Medtronic Activa PC+S Sensing Deep Brain Stimulator Generator | Other | Phase PHASE1 | Parkinson's Disease | WITHDRAWN | NCT02438033 |
| Zephyr BioPatch | Other | Preclinical | Physiologic Monitoring | COMPLETED | NCT02570906 |
| Zephyr BioPatch | Other | Preclinical | Physiologic Monitoring | COMPLETED | NCT02570906 |
| Scuba Iliac Stent System | Other | Approved | Peripheral Artery Disease | COMPLETED | NCT00880230 |
| Scuba Iliac Stent System | Other | Approved | Peripheral Artery Disease | COMPLETED | NCT00880230 |
| Minimed®640G system | Other | Preclinical | Type 1 Diabetes | COMPLETED | NCT02325193 |
| Minimed®640G system | Other | Preclinical | Type 1 Diabetes | COMPLETED | NCT02325193 |
| Minimed®640G system | Other | Preclinical | Type 1 Diabetes | COMPLETED | NCT02325193 |
| Capsule Endoscopy | Other | Approved | Ulcerative Colitis | COMPLETED | NCT02025777 |
| Capsule Endoscopy | Other | Approved | Ulcerative Colitis | COMPLETED | NCT02025777 |
| 2 Stents | Other | Approved | Percutaneous Transluminal Coronary Angioplasty | UNKNOWN | NCT02497014 |
| 1 Stent | Other | Approved | Percutaneous Transluminal Coronary Angioplasty | UNKNOWN | NCT02497014 |
| Cardiac Resynchronisation Therapy | Drug | Preclinical | Chronic Heart Failure | UNKNOWN | NCT02541773 |
| Non-coumadin Oral Anticoagulant | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT01706146 |
| Cardiac resynchronization therapy device implantation | Drug | Approved | Heart Failure | COMPLETED | NCT01996397 |
| Cardiac resynchronization therapy device implantation | Drug | Approved | Heart Failure | COMPLETED | NCT01996397 |
| Cardiac resynchronization therapy device implantation | Drug | Approved | Heart Failure | COMPLETED | NCT01996397 |
| Assurant® Cobalt Iliac Stent System | Other | Approved | Peripheral Vascular Disease | COMPLETED | NCT00753337 |
| Assurant® Cobalt Iliac Stent System | Other | Approved | Peripheral Vascular Disease | COMPLETED | NCT00753337 |
| Holter Recording_ NEMon DR220 Holter Recorders | Other | Approved | Atrial Fibrillation | TERMINATED | NCT02530203 |
| Spinal Cord Stimulation System | Other | Approved | Atrial Fibrillation | TERMINATED | NCT02530203 |
| Holter Recording_ NEMon DR220 Holter Recorders | Other | Approved | Atrial Fibrillation | TERMINATED | NCT02530203 |
| Spinal Cord Stimulation System | Other | Approved | Atrial Fibrillation | TERMINATED | NCT02530203 |
| Left ventricular septum pacing lead | Other | Preclinical | Left Ventricular Dysfunction | COMPLETED | NCT01609738 |
| Left ventricular septum pacing lead | Other | Preclinical | Left Ventricular Dysfunction | COMPLETED | NCT01609738 |
| Left ventricular septum pacing lead | Other | Preclinical | Left Ventricular Dysfunction | COMPLETED | NCT01609738 |
| Open Loop | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02040571 |
| Closed Loop | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02040571 |
| Medtronic MiniMed 620G or 640G Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01726621 |
| Medtronic MiniMed 620G or 640G Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01726621 |
| PAV | Other | Approved | Weaning From Mechanical Ventilation | COMPLETED | NCT01666054 |
| PSV | Other | Approved | Weaning From Mechanical Ventilation | COMPLETED | NCT01666054 |
| PAV | Other | Approved | Weaning From Mechanical Ventilation | COMPLETED | NCT01666054 |
| PSV | Other | Approved | Weaning From Mechanical Ventilation | COMPLETED | NCT01666054 |
| PAV | Other | Approved | Weaning From Mechanical Ventilation | COMPLETED | NCT01666054 |
| PSV | Other | Approved | Weaning From Mechanical Ventilation | COMPLETED | NCT01666054 |
| Sapheon™ Closure System | Other | Approved | Venous Insufficiency of Leg | COMPLETED | NCT01603433 |
| Sapheon™ Closure System | Other | Approved | Venous Insufficiency of Leg | COMPLETED | NCT01603433 |
| CE Marked Sapheon Closure System | Other | Approved | Venous Insufficiency of Leg | COMPLETED | NCT01570101 |
| CE Marked Sapheon Closure System | Other | Approved | Venous Insufficiency of Leg | COMPLETED | NCT01570101 |
| BRYAN Cervical Disc Prosthesis | Other | Approved | Radiculopathy | COMPLETED | NCT00437190 |
| ATLANTIS™ Cervical Plate System and allograft | Other | Approved | Radiculopathy | COMPLETED | NCT00437190 |
| BRYAN Cervical Disc Prosthesis | Other | Approved | Radiculopathy | COMPLETED | NCT00437190 |
| ATLANTIS™ Cervical Plate System and allograft | Other | Approved | Radiculopathy | COMPLETED | NCT00437190 |
| MDT-10013 | Other | Phase PHASE2 | Post-operation Pain | WITHDRAWN | NCT02263222 |
| MDT-10013 | Other | Phase PHASE2 | Post-operation Pain | WITHDRAWN | NCT02263222 |
| MDT-10013 | Other | Phase PHASE2 | Post-operation Pain | WITHDRAWN | NCT02263222 |
| ATS 3f® Aortic Bioprosthesis, Model 1000, 19mm | Other | Approved | Heart Valve Diseases | TERMINATED | NCT00657826 |
| ATS 3f® Aortic Bioprosthesis, Model 1000, 19mm | Other | Approved | Heart Valve Diseases | TERMINATED | NCT00657826 |
| Enlite 3 Sensor | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02649010 |
| Enlite 3 Sensor | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02649010 |
| Managed Ventricular Pacing programmed ON/OFF | Other | Phase PHASE4 | Cardiovascular Diseases | COMPLETED | NCT00293241 |
| Managed Ventricular Pacing programmed ON/OFF | Other | Phase PHASE4 | Cardiovascular Diseases | COMPLETED | NCT00293241 |
| Radiofrequency Ablation (Barrx™) | Other | Approved | Anal Intraepithelial Neoplasia (AIN) | COMPLETED | NCT02189161 |
| Radiofrequency Ablation (Barrx™) | Other | Approved | Anal Intraepithelial Neoplasia (AIN) | COMPLETED | NCT02189161 |
| Aquamantys® probe for liver hemostasis | Other | Phase PHASE2 | Hepatectomy | UNKNOWN | NCT01874639 |
| standard bipolar coagulation | Other | Phase PHASE2 | Hepatectomy | UNKNOWN | NCT01874639 |
| Aquamantys® probe for liver hemostasis | Other | Phase PHASE2 | Hepatectomy | UNKNOWN | NCT01874639 |
| standard bipolar coagulation | Other | Phase PHASE2 | Hepatectomy | UNKNOWN | NCT01874639 |
| lowering of the performance level of an adjustable Strata valve in a ventriculoperitoneal (VP) shunt for treating idiopathic normal pressure hydrocephalus | Other | Approved | Idiopathic Normal Pressure Hydrocephalus | COMPLETED | NCT01570257 |
| Implantable Cardioverter Defibrillator | Other | Preclinical | Implantable Defibrillator User | COMPLETED | NCT02491853 |
| Passive Leg Raise (PLR) | Other | Preclinical | Shock | COMPLETED | NCT01656954 |
| Passive Leg Raise (PLR) | Other | Preclinical | Shock | COMPLETED | NCT01656954 |
| Passive Leg Raise (PLR) | Other | Preclinical | Shock | COMPLETED | NCT01656954 |
| Electromagnetic Sinus Dilation System (NuVent™) | Other | Approved | Chronic Rhinosinusitis | COMPLETED | NCT02284347 |
| Electromagnetic Sinus Dilation System (NuVent™) | Other | Approved | Chronic Rhinosinusitis | COMPLETED | NCT02284347 |
| Electromagnetic Sinus Dilation System (NuVent™) | Other | Approved | Chronic Rhinosinusitis | COMPLETED | NCT02284347 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT01832493 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT01832493 |
| Provocative Discography | Other | Phase PHASE4 | Discogenic Pain | WITHDRAWN | NCT01077947 |
| Functional anesthetic discography | Other | Phase PHASE4 | Discogenic Pain | WITHDRAWN | NCT01077947 |
| Provocative Discography | Other | Phase PHASE4 | Discogenic Pain | WITHDRAWN | NCT01077947 |
| Functional anesthetic discography | Other | Phase PHASE4 | Discogenic Pain | WITHDRAWN | NCT01077947 |
| Provocative Discography | Other | Phase PHASE4 | Discogenic Pain | WITHDRAWN | NCT01077947 |
| Functional anesthetic discography | Other | Phase PHASE4 | Discogenic Pain | WITHDRAWN | NCT01077947 |
| Insertable Cardiac Monitor Implant | Other | Approved | Syncope | COMPLETED | NCT01965899 |
| Ablation | Other | Preclinical | Paroxysmal Atrial Fibrillation | WITHDRAWN | NCT01877486 |
| clonidine | Other | Phase PHASE2 | Hypertension | COMPLETED | NCT01297335 |
| Indoor rowing | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT02444156 |
| Model 20105 | Other | Approved | Sick Sinus Node Syndrome | TERMINATED | NCT02301429 |
| Model 20105 | Other | Approved | Sick Sinus Node Syndrome | TERMINATED | NCT02301429 |
| Model 20105 | Other | Approved | Sick Sinus Node Syndrome | TERMINATED | NCT02301429 |
| Medtronic Multi-electrode Radiofrequency (RF) Renal Denervation system | Other | Approved | Uncontrolled Hypertension | COMPLETED | NCT01699529 |
| Medtronic Multi-electrode Radiofrequency (RF) Renal Denervation system | Other | Approved | Uncontrolled Hypertension | COMPLETED | NCT01699529 |
| MERCI® Device | Device | Approved | Ischemic Stroke | COMPLETED | NCT01054560 |
| SOLITAIRE™ Device | Device | Approved | Ischemic Stroke | COMPLETED | NCT01054560 |
| MERCI® Device | Device | Approved | Ischemic Stroke | COMPLETED | NCT01054560 |
| SOLITAIRE™ Device | Device | Approved | Ischemic Stroke | COMPLETED | NCT01054560 |
| MERCI® Device | Device | Approved | Ischemic Stroke | COMPLETED | NCT01054560 |
| SOLITAIRE™ Device | Device | Approved | Ischemic Stroke | COMPLETED | NCT01054560 |
| 640G Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02246582 |
| Guardian Mobile App | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02246582 |
| Enlite 3 | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02246582 |
| 640G Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02246582 |
| Guardian Mobile App | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02246582 |
| Enlite 3 | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02246582 |
| Prevadh film | Other | Phase PHASE4 | Uterine Fibroids | COMPLETED | NCT01388907 |
| Ringer lactate solution | Other | Phase PHASE4 | Uterine Fibroids | COMPLETED | NCT01388907 |
| Prevadh film | Other | Phase PHASE4 | Uterine Fibroids | COMPLETED | NCT01388907 |
| Ringer lactate solution | Other | Phase PHASE4 | Uterine Fibroids | COMPLETED | NCT01388907 |
| On-pump bypass surgery | Procedure | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01290952 |
| Off-pump bypass surgery | Procedure | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01290952 |
| On-pump bypass surgery | Procedure | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01290952 |
| Off-pump bypass surgery | Procedure | Phase PHASE4 | Coronary Artery Disease | COMPLETED | NCT01290952 |
| Device: Attain Performa Pacing Lead (along with a standard CRT-D system) | Device | Approved | Heart Failure | COMPLETED | NCT01751022 |
| Device: Attain Performa Pacing Lead (along with a standard CRT-D system) | Device | Approved | Heart Failure | COMPLETED | NCT01751022 |
| Not device O-Arm in RAQUIS | Device | Approved | Surgical Incision | UNKNOWN | NCT02989363 |
| Not device O-Arm in DBS | Device | Approved | Surgical Incision | UNKNOWN | NCT02989363 |
| Device O-Arm in RAQUIS | Device | Approved | Surgical Incision | UNKNOWN | NCT02989363 |
| Device O-Arm in DBS | Device | Approved | Surgical Incision | UNKNOWN | NCT02989363 |
| Dual Site Pacing | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT01213251 |
| Single Site Pacing | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT01213251 |
| Dual Site Pacing | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT01213251 |
| Single Site Pacing | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT01213251 |
| Dual Site Pacing | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT01213251 |
| Single Site Pacing | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT01213251 |
| Diclofenac hydroxyethylpyrrolidine | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| PENNSAID | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| Diclofenac hydroxyethylpyrrolidine | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| PENNSAID | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| Diclofenac hydroxyethylpyrrolidine | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| PENNSAID | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| Diclofenac hydroxyethylpyrrolidine | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| PENNSAID | Other | Approved | Pain | WITHDRAWN | NCT01350622 |
| implantable heart rate monitor | Other | Approved | Epilepsy | COMPLETED | NCT01946776 |
| IN.PACT Admiral Paclitaxel-Eluting Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter | Other | Approved | Atherosclerosis | COMPLETED | NCT02118532 |
| IN.PACT Admiral Paclitaxel-Eluting Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter | Other | Approved | Atherosclerosis | COMPLETED | NCT02118532 |
| Conducted AF Response Plus (CAFRPlus) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02222818 |
| Conducted AF Response (CAFR) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02222818 |
| Conducted AF Response Plus (CAFRPlus) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02222818 |
| Conducted AF Response (CAFR) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02222818 |
| MD Logic Pump Advisor | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01308164 |
| MD Logic Pump Advisor | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01157923 |
| HET Bipolar System | Other | Approved | Hemorrhoids, Internal | COMPLETED | NCT01841970 |
| HET Bipolar System | Other | Approved | Hemorrhoids, Internal | COMPLETED | NCT01841970 |
| Solitaire™ FR device | Device | Preclinical | Stroke, Acute | COMPLETED | NCT01327989 |
| Solitaire™ FR device | Device | Preclinical | Stroke, Acute | COMPLETED | NCT01327989 |
| Solitaire™ FR device | Device | Preclinical | Stroke, Acute | COMPLETED | NCT01327989 |
| Renal sympathetic denervation | Other | Phase PHASE3 | Hypertension | COMPLETED | NCT01850901 |
| Renal Denervation | Other | Approved | Heart Failure | TERMINATED | NCT01392196 |
| Renal Denervation | Other | Approved | Heart Failure | TERMINATED | NCT01392196 |
| Renal Denervation | Other | Approved | Heart Failure | TERMINATED | NCT01392196 |
| Spine Fusion | Other | Preclinical | Spine Fusion | COMPLETED | NCT02280187 |
| Spine Fusion | Other | Preclinical | Spine Fusion | COMPLETED | NCT02280187 |
| Duplex ultra sound screening for abdominal aortic aneurysms | Other | Approved | Abdominal Aortic Aneurysm (AAA) | COMPLETED | NCT02306304 |
| Standalone Decompressive Surgery | Procedure | Phase PHASE4 | Spinal Stenosis | COMPLETED | NCT00905359 |
| Aperius™ PercLID™ System | Other | Phase PHASE4 | Spinal Stenosis | COMPLETED | NCT00905359 |
| Standalone Decompressive Surgery | Procedure | Phase PHASE4 | Spinal Stenosis | COMPLETED | NCT00905359 |
| Aperius™ PercLID™ System | Other | Phase PHASE4 | Spinal Stenosis | COMPLETED | NCT00905359 |
| Defibrillation following induction of VT/VF | Other | Approved | Ventricular Arrhythmias | TERMINATED | NCT02227121 |
| Defibrillation following induction of VT/VF | Other | Approved | Ventricular Arrhythmias | TERMINATED | NCT02227121 |
| Aspirin plus clopidogrel | Other | Phase PHASE4 | Coronary Artery Disease | TERMINATED | NCT02494284 |
| Clopidogrel | Other | Phase PHASE4 | Coronary Artery Disease | TERMINATED | NCT02494284 |
| Cardiac Resynchronization Therapy | Drug | Approved | Heart Failure | COMPLETED | NCT02326493 |
| control group | Other | Approved | Aortic Stenosis | COMPLETED | NCT02504632 |
| test | Other | Approved | Aortic Stenosis | COMPLETED | NCT02504632 |
| MDT-4107 Zotarolimus-Eluting Coronary Stent | Other | Approved | Arterial Occlusive Diseases | COMPLETED | NCT01150500 |
| MDT-4107 Zotarolimus-Eluting Coronary Stent | Other | Approved | Arterial Occlusive Diseases | COMPLETED | NCT01150500 |
| Control | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT02366767 |
| Automatic closed-loop insulin delivery | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT02366767 |
| Endeavor Resolute Stent | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT00850213 |
| Endeavor Resolute Stent | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT00850213 |
| Balloon kyphoplasty | Other | Approved | Compression Fracture of Vertebral Body | COMPLETED | NCT01871519 |
| Balloon kyphoplasty | Other | Approved | Compression Fracture of Vertebral Body | COMPLETED | NCT01871519 |
| Advantage Prosthetic Heart Valve | Other | Preclinical | Heart Valve Stenosis | TERMINATED | NCT01264484 |
| Advantage Prosthetic Heart Valve | Other | Preclinical | Heart Valve Stenosis | TERMINATED | NCT01264484 |
| Advantage Prosthetic Heart Valve | Other | Preclinical | Heart Valve Stenosis | TERMINATED | NCT01264484 |
| Endo GIA™ Reinforced Reload with Tri-Staple™ Technology | Other | Approved | Non-emergent, Abdominal or Thoracic Procedures | COMPLETED | NCT02500537 |
| Endo GIA™ Reinforced Reload with Tri-Staple™ Technology | Other | Approved | Non-emergent, Abdominal or Thoracic Procedures | COMPLETED | NCT02500537 |
| Zephyr BioPatch | Other | Preclinical | Patient Positioning | WITHDRAWN | NCT02548624 |
| Zephyr BioPatch | Other | Preclinical | Patient Positioning | WITHDRAWN | NCT02548624 |
| Zephyr BioPatch | Other | Preclinical | Patient Positioning | WITHDRAWN | NCT02548624 |
| pacemaker programming to mode switch to atrial pacing versus atrioventricular hysteresis function | Other | Approved | Pacemaker Implantation for Sinus Node Disease | COMPLETED | NCT01803217 |
| Current Infusion Set | Other | Preclinical | Type 1 Diabetes Mellitus | COMPLETED | NCT02662842 |
| FlowSmart Infusion Set | Other | Preclinical | Type 1 Diabetes Mellitus | COMPLETED | NCT02662842 |
| Continuous Glucose Monitoring with treatment algorithm | Drug | Approved | DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (Disorder) | COMPLETED | NCT01614262 |
| MDT-15 | Other | Phase PHASE2 | Sciatica | COMPLETED | NCT01917825 |
| MDT-15 | Other | Phase PHASE2 | Sciatica | COMPLETED | NCT01917825 |
| Various | Other | Preclinical | Spinal Cord Stimulation | COMPLETED | NCT00959296 |
| Various | Other | Preclinical | Spinal Cord Stimulation | COMPLETED | NCT00959296 |
| Various | Other | Preclinical | Spinal Cord Stimulation | COMPLETED | NCT00959296 |
| RV lead placement site | Other | Approved | Left Ventricular Dysfunction | COMPLETED | NCT00461734 |
| RV lead placement site | Other | Approved | Left Ventricular Dysfunction | COMPLETED | NCT00461734 |
| Renal Angiography | Other | Approved | Hypertension | COMPLETED | NCT01972139 |
| Sham Renal Denervation | Other | Approved | Hypertension | COMPLETED | NCT01972139 |
| Renal Denervation using the Symplicity Renal Denervation System | Other | Approved | Hypertension | COMPLETED | NCT01972139 |
| Renal Angiography | Other | Approved | Hypertension | COMPLETED | NCT01972139 |
| Sham Renal Denervation | Other | Approved | Hypertension | COMPLETED | NCT01972139 |
| Renal Denervation using the Symplicity Renal Denervation System | Other | Approved | Hypertension | COMPLETED | NCT01972139 |
| Standard of care | Other | Approved | Parkinson's Disease | WITHDRAWN | NCT02541617 |
| Programming by community Neurologist | Other | Approved | Parkinson's Disease | WITHDRAWN | NCT02541617 |
| Nellcor USB Pulse Oximeter Monitor Interface Cable | Other | Approved | Healthy Volunteers | COMPLETED | NCT02265783 |
| Nellcor USB Pulse Oximeter Monitor Interface Cable | Other | Approved | Healthy Volunteers | COMPLETED | NCT02265783 |
| SIPS the stomach, intestinal, pylorus, sparing procedure | Procedure | Preclinical | Obesity | COMPLETED | NCT02275208 |
| SIPS the stomach, intestinal, pylorus, sparing procedure | Procedure | Preclinical | Obesity | COMPLETED | NCT02275208 |
| Atrial fibrillation ablation | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT02294929 |
| Resolute Onyx | Other | Preclinical | Coronary Artery Disease | UNKNOWN | NCT03151018 |
| Rocuronium 0.6 mg/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| Rocuronium 0.4 mg/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| Rocuronium 0.2 mg/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| Saline 0.06 ml/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| Rocuronium 0.6 mg/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| Rocuronium 0.4 mg/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| Rocuronium 0.2 mg/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| Saline 0.06 ml/kg | Other | Approved | Anesthesia | COMPLETED | NCT01450813 |
| MiniMed® 640G Insulin Pump and Guardian® Link Transmitter | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01991548 |
| MiniMed® 640G Insulin Pump and Guardian® Link Transmitter | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01991548 |
| MiniMed® 640G Insulin Pump and Guardian® Link Transmitter | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01991548 |
| PTA Balloon: Balloon Angioplasty | Other | Approved | Peripheral Arterial Disease (PAD) | COMPLETED | NCT01175850 |
| Drug-Coated Balloon (DCB) | Drug | Approved | Peripheral Arterial Disease (PAD) | COMPLETED | NCT01175850 |
| PTA Balloon: Balloon Angioplasty | Other | Approved | Peripheral Arterial Disease (PAD) | COMPLETED | NCT01175850 |
| Drug-Coated Balloon (DCB) | Drug | Approved | Peripheral Arterial Disease (PAD) | COMPLETED | NCT01175850 |
| ATS 3f Aortic Bioprosthesis | Other | Approved | Heart Valve Diseases | TERMINATED | NCT01116037 |
| ATS 3f Aortic Bioprosthesis | Other | Approved | Heart Valve Diseases | TERMINATED | NCT01116037 |
| ATS 3f Aortic Bioprosthesis | Other | Approved | Heart Valve Diseases | TERMINATED | NCT01116037 |
| Metoprolol | Other | Phase PHASE2 | Cardiac Arrest | TERMINATED | NCT00401882 |
| Epinephrine | Other | Phase PHASE2 | Cardiac Arrest | TERMINATED | NCT00401882 |
| Metoprolol | Other | Phase PHASE2 | Cardiac Arrest | TERMINATED | NCT00401882 |
| Epinephrine | Other | Phase PHASE2 | Cardiac Arrest | TERMINATED | NCT00401882 |
| Capsule endoscopy and Ileocolonoscopy tests | Other | Approved | Known Crohn Disease Subjects | COMPLETED | NCT01942720 |
| Capsule endoscopy and Ileocolonoscopy tests | Other | Approved | Known Crohn Disease Subjects | COMPLETED | NCT01942720 |
| ECG and survey screening | Other | Preclinical | Sudden Cardiac Death | UNKNOWN | NCT01845909 |
| Paradigm 715 insulin pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00211510 |
| Paradigm 722 sensor augmented pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00211510 |
| Paradigm 715 insulin pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00211510 |
| Paradigm 722 sensor augmented pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT00211510 |
| CoreValve System Family | Other | Preclinical | Symptomatic Aortic Stenosis | TERMINATED | NCT02759237 |
| [STN+SNr] | Other | Approved | Parkinson's Disease | UNKNOWN | NCT02588144 |
| [standard STN] | Other | Approved | Parkinson's Disease | UNKNOWN | NCT02588144 |
| MDT-2211 Renal Denervation System | Other | Approved | Uncontrolled Hypertension | COMPLETED | NCT01644604 |
| MDT-2211 Renal Denervation System | Other | Approved | Uncontrolled Hypertension | COMPLETED | NCT01644604 |
| PillCam ESO Capsule Endoscope | Other | Approved | Esophageal Lesion | COMPLETED | NCT00990782 |
| PillCam ESO Capsule Endoscope | Other | Approved | Esophageal Lesion | COMPLETED | NCT00990782 |
| CGMS Gold | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01921322 |
| Pump | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01921322 |
| CGMS Gold | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01921322 |
| Pump | Other | Approved | Type 2 Diabetes | COMPLETED | NCT01921322 |
| Roux-en-Y Gastric Bypass | Other | Preclinical | Morbid Obesity | COMPLETED | NCT01754194 |
| Gastric Sleeve Resection | Other | Preclinical | Morbid Obesity | COMPLETED | NCT01754194 |
| Roux-en-Y Gastric Bypass | Other | Preclinical | Morbid Obesity | COMPLETED | NCT01754194 |
| Gastric Sleeve Resection | Other | Preclinical | Morbid Obesity | COMPLETED | NCT01754194 |
| Endovenous Laser | Other | Phase PHASE4 | Venous Reflux | COMPLETED | NCT00509392 |
| Seg. RF Ablation & ClosureFAST catheter | Other | Phase PHASE4 | Venous Reflux | COMPLETED | NCT00509392 |
| Endovenous Laser | Other | Phase PHASE4 | Venous Reflux | COMPLETED | NCT00509392 |
| Seg. RF Ablation & ClosureFAST catheter | Other | Phase PHASE4 | Venous Reflux | COMPLETED | NCT00509392 |
| registration of AdaptiveStim | Other | Approved | Failed Back Surgery Syndrome | COMPLETED | NCT02974101 |
| Initial bolus pre-incision | Other | Approved | Hemodynamic Instability | TERMINATED | NCT02365688 |
| Initial bolus pre-incision | Other | Approved | Hemodynamic Instability | TERMINATED | NCT02365688 |
| Optimal Medical Management (OMM) | Other | Phase PHASE4 | Failed Back Surgery Syndrome | COMPLETED | NCT01697358 |
| Spinal Cord Stimulation (SCS) | Other | Phase PHASE4 | Failed Back Surgery Syndrome | COMPLETED | NCT01697358 |
| Optimal Medical Management (OMM) | Other | Phase PHASE4 | Failed Back Surgery Syndrome | COMPLETED | NCT01697358 |
| Spinal Cord Stimulation (SCS) | Other | Phase PHASE4 | Failed Back Surgery Syndrome | COMPLETED | NCT01697358 |
| Closed Loop Insulin | Other | Approved | Chronic Pancreatitis | COMPLETED | NCT01945138 |
| Closed Loop Insulin | Other | Approved | Chronic Pancreatitis | COMPLETED | NCT01945138 |
| Low-carbohydrate diet with post-meal walking | Other | Approved | Type 2 Diabetes | COMPLETED | NCT02683135 |
| Low-carbohydrate diet | Other | Approved | Type 2 Diabetes | COMPLETED | NCT02683135 |
| High-carbohydrate diet | Other | Approved | Type 2 Diabetes | COMPLETED | NCT02683135 |
| Axium™ MicroFX™ PGLA COILS | Other | Preclinical | Aneurysm | COMPLETED | NCT01323439 |
| Axium™ MicroFX™ PGLA COILS | Other | Preclinical | Aneurysm | COMPLETED | NCT01323439 |
| 12 months DAPT | Other | Phase PHASE4 | Myocardial Infarction | COMPLETED | NCT01459627 |
| 6 months DAPT | Other | Phase PHASE4 | Myocardial Infarction | COMPLETED | NCT01459627 |
| Standard of Care | Other | Approved | Elective Cranial Procedures With Dural Incision | COMPLETED | NCT00704340 |
| DuraSeal Dural Sealant System | Other | Approved | Elective Cranial Procedures With Dural Incision | COMPLETED | NCT00704340 |
| Standard of Care | Other | Approved | Elective Cranial Procedures With Dural Incision | COMPLETED | NCT00704340 |
| DuraSeal Dural Sealant System | Other | Approved | Elective Cranial Procedures With Dural Incision | COMPLETED | NCT00704340 |
| Standard of Care | Other | Approved | Cerebrospinal Fluid Leakage, Subdural | COMPLETED | NCT00444067 |
| Spinal Sealant | Other | Approved | Cerebrospinal Fluid Leakage, Subdural | COMPLETED | NCT00444067 |
| Standard of Care | Other | Approved | Cerebrospinal Fluid Leakage, Subdural | COMPLETED | NCT00444067 |
| Spinal Sealant | Other | Approved | Cerebrospinal Fluid Leakage, Subdural | COMPLETED | NCT00444067 |
| PillCam SBC system | Other | Approved | Chronic Inflammatory Small Bowel Disease | COMPLETED | NCT02742714 |
| PillCam SBC system | Other | Approved | Chronic Inflammatory Small Bowel Disease | COMPLETED | NCT02742714 |
| Spinal Cord Stimulation (SCS) | Other | Approved | Pain, Intractable | COMPLETED | NCT02503787 |
| Spinal Cord Stimulation (SCS) | Other | Approved | Pain, Intractable | COMPLETED | NCT02503787 |
| Spinal Cord Stimulation (SCS) | Other | Approved | Pain, Intractable | COMPLETED | NCT02503787 |
| PrimeAdvanced® neurostimulator system | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01818297 |
| PrimeAdvanced® neurostimulator system | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01818297 |
| PrimeAdvanced® neurostimulator system | Other | Approved | Failed Back Surgery Syndrome | TERMINATED | NCT01818297 |
| Predictive Low Glucose Management Feature in Insulin pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02130284 |
| Predictive Low Glucose Management Feature in Insulin pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02130284 |
| TTR controller (Medtronic) | Other | Approved | Diabetes Mellitus | COMPLETED | NCT01490151 |
| hosptial setting | Other | Approved | Arrhythmia | COMPLETED | NCT02395536 |
| office setting | Other | Approved | Arrhythmia | COMPLETED | NCT02395536 |
| hosptial setting | Other | Approved | Arrhythmia | COMPLETED | NCT02395536 |
| office setting | Other | Approved | Arrhythmia | COMPLETED | NCT02395536 |
| Autologous bone graft | Other | Phase PHASE1 | Bone Degenerative Changes | COMPLETED | NCT01690260 |
| Bone Morphogenetic Protein 2 | Other | Phase PHASE1 | Bone Degenerative Changes | COMPLETED | NCT01690260 |
| Resolute Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT01334268 |
| Taxus Liberte Paclitaxel-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT01334268 |
| Resolute Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT01334268 |
| Taxus Liberte Paclitaxel-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT01334268 |
| Small bowel RFA treatment | Drug | Approved | Angiodysplasia | WITHDRAWN | NCT03320395 |
| Pillcam endoscopy system | Other | Approved | Any Gastric Condition Which Requires Capsule Endoscopy | COMPLETED | NCT02775708 |
| Pillcam endoscopy system | Other | Approved | Any Gastric Condition Which Requires Capsule Endoscopy | COMPLETED | NCT02775708 |
| Magnetic resonance imaging | Other | Preclinical | Anal Sphincter Injury | COMPLETED | NCT03039374 |
| CRT-P OFF | Other | Approved | Congestive Heart Failure | TERMINATED | NCT01735916 |
| CRT-P Implant | Other | Approved | Congestive Heart Failure | TERMINATED | NCT01735916 |
| CRT-P OFF | Other | Approved | Congestive Heart Failure | TERMINATED | NCT01735916 |
| CRT-P Implant | Other | Approved | Congestive Heart Failure | TERMINATED | NCT01735916 |
| Protecta DR-ICD or CRT-D | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00982397 |
| Protecta VR-ICD | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00982397 |
| Protecta DR-ICD or CRT-D | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00982397 |
| Protecta VR-ICD | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00982397 |
| Protecta DR-ICD or CRT-D | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00982397 |
| Protecta VR-ICD | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00982397 |
| Sham procedure plus anti-secretory medication | Drug | Approved | Barrett Esophagus | COMPLETED | NCT00282672 |
| Ablation System plus anti-secretory medication | Drug | Approved | Barrett Esophagus | COMPLETED | NCT00282672 |
| Sham procedure plus anti-secretory medication | Drug | Approved | Barrett Esophagus | COMPLETED | NCT00282672 |
| Ablation System plus anti-secretory medication | Drug | Approved | Barrett Esophagus | COMPLETED | NCT00282672 |
| Harmony 1 Sensor | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02646878 |
| Harmony 1 Sensor | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02646878 |
| Aortic Valve Replacement | Other | Preclinical | Aortic Valve Stenosis | TERMINATED | NCT01636648 |
| Aortic Valve Replacement | Other | Preclinical | Aortic Valve Stenosis | TERMINATED | NCT01636648 |
| Continuous glucose monitoring | Other | Approved | Gestational Diabetes | UNKNOWN | NCT03326232 |
| Implantable neurostimulation system | Other | Approved | Chronic and Severe Post-coma Disorders of Consciousness (Permanent Vegetative State, Minimally Conscious State) | COMPLETED | NCT01718249 |
| RYGB & IMM | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00641251 |
| intensive medical management | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00641251 |
| RYGB & IMM | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00641251 |
| intensive medical management | Other | Approved | Type 2 Diabetes | COMPLETED | NCT00641251 |
| SmartPill Monitoring System | Other | Approved | Gastroparesis | TERMINATED | NCT02022826 |
| SmartPill Monitoring System | Other | Approved | Gastroparesis | TERMINATED | NCT02022826 |
| Pacing | Other | Approved | First-degree AV-block | COMPLETED | NCT01985802 |
| Chronicle Implantable Hemodynamic Monitor (IHM) System, Chronicle Implantable Cardioverter Defibrillator (ICD) | Other | Preclinical | Heart Failure | COMPLETED | NCT00991120 |
| Chronicle Implantable Hemodynamic Monitor (IHM) System, Chronicle Implantable Cardioverter Defibrillator (ICD) | Other | Preclinical | Heart Failure | COMPLETED | NCT00991120 |
| Chronicle Implantable Hemodynamic Monitor (IHM) System, Chronicle Implantable Cardioverter Defibrillator (ICD) | Other | Preclinical | Heart Failure | COMPLETED | NCT00991120 |
| Medtronic CoreValve System | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01074658 |
| Medtronic CoreValve System | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01074658 |
| Medtronic CoreValve System | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01074658 |
| No-CRT | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT01434615 |
| CRT | Other | Phase PHASE4 | Heart Failure | COMPLETED | NCT01434615 |
| O2/CO2 cannula w/female luer (Westmed comfort plus #0504) | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Experimental sample line Model 5 | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Experimental sample line Model 4 | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Experimental sample line Model 3 | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Oridion Smart CapnoLine® Plus with Non-Wedge cannula | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Oridion Smart CapnoLine® H Plus with Wedge cannula | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| O2/CO2 cannula w/female luer (Westmed comfort plus #0504) | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Experimental sample line Model 5 | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Experimental sample line Model 4 | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Experimental sample line Model 3 | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Oridion Smart CapnoLine® Plus with Non-Wedge cannula | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Oridion Smart CapnoLine® H Plus with Wedge cannula | Other | Approved | Wearing Comfort | COMPLETED | NCT03109132 |
| Laminectomy | Other | Phase PHASE4 | Lumbar Spinal Stenosis | WITHDRAWN | NCT00558129 |
| X-STOP® | Other | Phase PHASE4 | Lumbar Spinal Stenosis | WITHDRAWN | NCT00558129 |
| Laminectomy | Other | Phase PHASE4 | Lumbar Spinal Stenosis | WITHDRAWN | NCT00558129 |
| X-STOP® | Other | Phase PHASE4 | Lumbar Spinal Stenosis | WITHDRAWN | NCT00558129 |
| Balloon Kyphoplasty | Other | Phase PHASE4 | Osteopenia | COMPLETED | NCT00211211 |
| Balloon Kyphoplasty | Other | Phase PHASE4 | Osteopenia | COMPLETED | NCT00211211 |
| InterStim® (Device Programming) | Device | Approved | Urinary Urge Incontinence | COMPLETED | NCT01957137 |
| InterStim® (Device Programming) | Device | Approved | Urinary Urge Incontinence | COMPLETED | NCT01957137 |
| InterStim® (Device Programming) | Device | Approved | Urinary Urge Incontinence | COMPLETED | NCT01957137 |
| Standard Medical Therapy | Drug | Phase PHASE4 | Urinary Incontinence, Urgency-frequency | COMPLETED | NCT00547378 |
| InterStim | Other | Phase PHASE4 | Urinary Incontinence, Urgency-frequency | COMPLETED | NCT00547378 |
| Standard Medical Therapy | Drug | Phase PHASE4 | Urinary Incontinence, Urgency-frequency | COMPLETED | NCT00547378 |
| InterStim | Other | Phase PHASE4 | Urinary Incontinence, Urgency-frequency | COMPLETED | NCT00547378 |
| Standard Medical Therapy | Drug | Phase PHASE4 | Urinary Incontinence, Urgency-frequency | COMPLETED | NCT00547378 |
| InterStim | Other | Phase PHASE4 | Urinary Incontinence, Urgency-frequency | COMPLETED | NCT00547378 |
| Four Port Laparoscopic Cholecystectomy | Other | Approved | Gallbladder Disease | COMPLETED | NCT00832767 |
| SILS™ port laparoscopic cholecystectomy | Other | Approved | Gallbladder Disease | COMPLETED | NCT00832767 |
| Four Port Laparoscopic Cholecystectomy | Other | Approved | Gallbladder Disease | COMPLETED | NCT00832767 |
| SILS™ port laparoscopic cholecystectomy | Other | Approved | Gallbladder Disease | COMPLETED | NCT00832767 |
| X-STOP PEEK | Other | Phase PHASE4 | Lumbar Spinal Stenosis | TERMINATED | NCT00517751 |
| X-STOP PEEK | Other | Phase PHASE4 | Lumbar Spinal Stenosis | TERMINATED | NCT00517751 |
| Kyphoplasty | Other | Approved | Vertebral Body Compression Fractures | TERMINATED | NCT00323609 |
| Vertebroplasty | Other | Approved | Vertebral Body Compression Fractures | TERMINATED | NCT00323609 |
| Kyphoplasty | Other | Approved | Vertebral Body Compression Fractures | TERMINATED | NCT00323609 |
| Vertebroplasty | Other | Approved | Vertebral Body Compression Fractures | TERMINATED | NCT00323609 |
| Sensor wear | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT01112696 |
| Sensor wear | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT01112696 |
| Glucose sensor (Enlite) | Other | Approved | Diabetes | COMPLETED | NCT02423798 |
| Glucose sensor (Enlite) | Other | Approved | Diabetes | COMPLETED | NCT02423798 |
| Micra Pacemaker Implant | Other | Approved | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | COMPLETED | NCT02004873 |
| Micra Pacemaker Implant | Other | Approved | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | COMPLETED | NCT02004873 |
| Micra Pacemaker Implant | Other | Approved | Class I or II Indication for Implantation of a Single Chamber Ventricular Pacemaker According to ACC/AHA/HRS 2001 Guidelines and Any National Guidelines | COMPLETED | NCT02004873 |
| Hybrid-logic closed loop system | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02692547 |
| Hybrid-logic closed loop system | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02692547 |
| Reclaim® Deep Brain Stimulation | Other | Phase PHASE4 | Obsessive Compulsive Disorder | COMPLETED | NCT01135745 |
| Reclaim® Deep Brain Stimulation | Other | Phase PHASE4 | Obsessive Compulsive Disorder | COMPLETED | NCT01135745 |
| External Electrocardioversion | Other | Approved | Atrial Arrhythmia | COMPLETED | NCT02241382 |
| Internal Electrocardioversion | Other | Approved | Atrial Arrhythmia | COMPLETED | NCT02241382 |
| Lumbar Interbody Fusion | Other | Phase PHASE4 | Low Back Pain | TERMINATED | NCT00095095 |
| Lumbar Interbody Fusion | Other | Phase PHASE4 | Low Back Pain | TERMINATED | NCT00095095 |
| intrathecal baclofen | Other | Phase PHASE4 | Severe Spasticity | COMPLETED | NCT01032239 |
| intrathecal baclofen | Other | Phase PHASE4 | Severe Spasticity | COMPLETED | NCT01032239 |
| Activa PC+S | Other | Approved | Parkinson's Disease | COMPLETED | NCT01990313 |
| Cortical lead, 8 electrodes (Model 2976) with Synergy neurostimulator | Other | Phase PHASE3 | Pain, Intractable | TERMINATED | NCT00122915 |
| Cortical lead, 8 electrodes (Model 2976) with Synergy neurostimulator | Other | Phase PHASE3 | Pain, Intractable | TERMINATED | NCT00122915 |
| Reveal® DX or Reveal® XT Insertable Cardiac Monitor | Other | Preclinical | Arrhythmias, Cardiac | COMPLETED | NCT01168427 |
| Reveal® DX or Reveal® XT Insertable Cardiac Monitor | Other | Preclinical | Arrhythmias, Cardiac | COMPLETED | NCT01168427 |
| Reveal® DX or Reveal® XT Insertable Cardiac Monitor | Other | Preclinical | Arrhythmias, Cardiac | COMPLETED | NCT01168427 |
| Standard PTA | Other | Approved | Critical Lower Limb Ischemia | COMPLETED | NCT00941733 |
| IN.PACT Amphirion | Other | Approved | Critical Lower Limb Ischemia | COMPLETED | NCT00941733 |
| Standard PTA | Other | Approved | Critical Lower Limb Ischemia | COMPLETED | NCT00941733 |
| IN.PACT Amphirion | Other | Approved | Critical Lower Limb Ischemia | COMPLETED | NCT00941733 |
| Sedation, RASS Targeted | Other | Approved | Delirium | COMPLETED | NCT00469482 |
| Sedation,RASS Targeted plus BIS Monitoring | Other | Approved | Delirium | COMPLETED | NCT00469482 |
| Sedation, RASS Targeted | Other | Approved | Delirium | COMPLETED | NCT00469482 |
| Sedation,RASS Targeted plus BIS Monitoring | Other | Approved | Delirium | COMPLETED | NCT00469482 |
| Insulin Pump (Medtronic Minimed Paradigm® VEO) | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT01182493 |
| Insulin Pump (Medtronic Minimed Paradigm® VEO) | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT01182493 |
| RF ablation (ClosureFAST) | Other | Approved | Venous Reflux | COMPLETED | NCT00842296 |
| RF ablation (ClosureFAST) | Other | Approved | Venous Reflux | COMPLETED | NCT00842296 |
| Standard of Care | Other | Approved | Chronic Disease | COMPLETED | NCT02659280 |
| Adjunct Therapy | Drug | Approved | Chronic Disease | COMPLETED | NCT02659280 |
| Medtronic DBS Therapy for epilepsy | Drug | Phase PHASE3 | Epilepsy | COMPLETED | NCT00101933 |
| Medtronic DBS Therapy for epilepsy | Drug | Phase PHASE3 | Epilepsy | COMPLETED | NCT00101933 |
| Loop Recorder | Other | Preclinical | Arrhythmias, Cardiac | UNKNOWN | NCT02957006 |
| Placebo | Other | Approved | Pre-Diabetes | TERMINATED | NCT02393573 |
| Metformin | Other | Approved | Pre-Diabetes | TERMINATED | NCT02393573 |
| Placebo | Other | Approved | Pre-Diabetes | TERMINATED | NCT02393573 |
| Metformin | Other | Approved | Pre-Diabetes | TERMINATED | NCT02393573 |
| CPB High Dose | Other | Approved | Cardiopulmonary Bypass | COMPLETED | NCT02979158 |
| CPB Low Dose | Other | Approved | Cardiopulmonary Bypass | COMPLETED | NCT02979158 |
| Conventional Medicine | Other | Approved | Chronic Pain | TERMINATED | NCT01924182 |
| SynchroMed Infusion System and Intrathecal Morphine Sulfate | Other | Approved | Chronic Pain | TERMINATED | NCT01924182 |
| Conventional Medicine | Other | Approved | Chronic Pain | TERMINATED | NCT01924182 |
| SynchroMed Infusion System and Intrathecal Morphine Sulfate | Other | Approved | Chronic Pain | TERMINATED | NCT01924182 |
| Conventional Medicine | Other | Approved | Chronic Pain | TERMINATED | NCT01924182 |
| SynchroMed Infusion System and Intrathecal Morphine Sulfate | Other | Approved | Chronic Pain | TERMINATED | NCT01924182 |
| PVAC Ablation Procedure | Procedure | Approved | Atrial Fibrillation | COMPLETED | NCT01562912 |
| Radiofrequency Ablation Procedure | Procedure | Approved | Atrial Fibrillation | COMPLETED | NCT01562912 |
| Reveal XT implantable loop recorder | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01176617 |
| Micra Pacemaker Implant | Other | Approved | Bradycardia | COMPLETED | NCT02488681 |
| Reprogramming dual chamber pacemaker | Other | Preclinical | Sinus Node Dysfunction | COMPLETED | NCT02027909 |
| CareLink Remote Monitoring | Other | Phase PHASE4 | Pacemaker | COMPLETED | NCT00631709 |
| CareLink Remote Monitoring | Other | Phase PHASE4 | Pacemaker | COMPLETED | NCT00631709 |
| CareLink Remote Monitoring | Other | Phase PHASE4 | Pacemaker | COMPLETED | NCT00631709 |
| Engager Transcatheter Aortic Valve Implantation System | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02149654 |
| Engager Transcatheter Aortic Valve Implantation System | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02149654 |
| Engager Transcatheter Aortic Valve Implantation System | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02149654 |
| Surgical Resection | Other | Approved | Lung Cancer | COMPLETED | NCT02323854 |
| Ablation | Other | Approved | Lung Cancer | COMPLETED | NCT02323854 |
| Surgical Resection | Other | Approved | Lung Cancer | COMPLETED | NCT02323854 |
| Ablation | Other | Approved | Lung Cancer | COMPLETED | NCT02323854 |
| Surgical Resection | Other | Approved | Lung Cancer | COMPLETED | NCT02323854 |
| Ablation | Other | Approved | Lung Cancer | COMPLETED | NCT02323854 |
| Repair of RV-PA Conduit Disruption | Other | Approved | Pulmonary Stenosis | COMPLETED | NCT01824160 |
| Suprasensory | Other | Approved | Irritable Bowel Syndrome | COMPLETED | NCT01948973 |
| OFF | Other | Approved | Irritable Bowel Syndrome | COMPLETED | NCT01948973 |
| Subsensory | Other | Approved | Irritable Bowel Syndrome | COMPLETED | NCT01948973 |
| sacral nerve stimulation | Other | Approved | Irritable Bowel Syndrome | COMPLETED | NCT01950715 |
| Educated T shock setting | Other | Approved | Cardiomyopathy | COMPLETED | NCT02027883 |
| Nominal T shock setting | Other | Approved | Cardiomyopathy | COMPLETED | NCT02027883 |
| Atrial flutter ablation and pulmonary vein isolation | Other | Approved | Atrial Flutter | COMPLETED | NCT01521988 |
| Atrial flutter ablation | Other | Approved | Atrial Flutter | COMPLETED | NCT01521988 |
| FlorenceM | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT03101865 |
| Cryo Ablation catheter | Other | Approved | Premature Ventricular Contraction | UNKNOWN | NCT03086902 |
| Radiofrequency Ablation Catheter | Other | Approved | Premature Ventricular Contraction | UNKNOWN | NCT03086902 |
| Heparin | Other | Phase PHASE1 | Type 1 Diabetes | COMPLETED | NCT02687256 |
| Standard Infusion set | Other | Phase PHASE1 | Type 1 Diabetes | COMPLETED | NCT02687256 |
| Extended Wear infusion set | Other | Phase PHASE1 | Type 1 Diabetes | COMPLETED | NCT02687256 |
| Defibrillation following induction of VT/VF | Other | Approved | Tachycardia | COMPLETED | NCT02772380 |
| Defibrillation following induction of VT/VF | Other | Approved | Tachycardia | COMPLETED | NCT02772380 |
| Diuretic and Medication Suspension (DMS) | Drug | Phase PHASE4 | Heart Failure | UNKNOWN | NCT03245281 |
| Diuretic Increase (DI) | Other | Phase PHASE4 | Heart Failure | UNKNOWN | NCT03245281 |
| Diuretic Suspension (DS) | Other | Phase PHASE4 | Heart Failure | UNKNOWN | NCT03245281 |
| Diuretic and Medication Suspension (DMS) | Drug | Phase PHASE4 | Heart Failure | UNKNOWN | NCT03245281 |
| Diuretic Increase (DI) | Other | Phase PHASE4 | Heart Failure | UNKNOWN | NCT03245281 |
| Diuretic Suspension (DS) | Other | Phase PHASE4 | Heart Failure | UNKNOWN | NCT03245281 |
| respiration assessment | Other | Approved | Breathing Exercises | COMPLETED | NCT02828735 |
| respiration assessment | Other | Approved | Breathing Exercises | COMPLETED | NCT02828735 |
| Roll-in (VenaSeal SCS) | Other | Approved | Great Saphenous Vein (GSV) With Venous Reflux Disease | COMPLETED | NCT01807585 |
| ClosureFast Radiofrequency Ablation (RFA) | Other | Approved | Great Saphenous Vein (GSV) With Venous Reflux Disease | COMPLETED | NCT01807585 |
| VenaSeal SCS | Other | Approved | Great Saphenous Vein (GSV) With Venous Reflux Disease | COMPLETED | NCT01807585 |
| Roll-in (VenaSeal SCS) | Other | Approved | Great Saphenous Vein (GSV) With Venous Reflux Disease | COMPLETED | NCT01807585 |
| ClosureFast Radiofrequency Ablation (RFA) | Other | Approved | Great Saphenous Vein (GSV) With Venous Reflux Disease | COMPLETED | NCT01807585 |
| VenaSeal SCS | Other | Approved | Great Saphenous Vein (GSV) With Venous Reflux Disease | COMPLETED | NCT01807585 |
| ATS 3f Enable Aortic Bioprosthesis Model 6000 | Other | Approved | Heart Valve Diseases | COMPLETED | NCT01116024 |
| ATS 3f Enable Aortic Bioprosthesis Model 6000 | Other | Approved | Heart Valve Diseases | COMPLETED | NCT01116024 |
| Medical therapy | Drug | Approved | Heavy Menstrual Bleeding | COMPLETED | NCT02934789 |
| Hysteroscopic myomectomy with Truclear | Other | Approved | Heavy Menstrual Bleeding | COMPLETED | NCT02934789 |
| implant of cardiac device as per guidelines | Device | Preclinical | Educational Problems | UNKNOWN | NCT03577340 |
| Diuretics | Other | Phase PHASE2 | Heart Failure | COMPLETED | NCT01370564 |
| Diuretics | Other | Phase PHASE2 | Heart Failure | COMPLETED | NCT01370564 |
| Exenatide | Other | Phase PHASE4 | Brain Injuries | COMPLETED | NCT02058940 |
| Spinal Cord Stimulation | Other | Approved | Chronic Low Back Pain | UNKNOWN | NCT03586882 |
| PARIETEX™ Composite Ventral Patch | Other | Preclinical | Hernia | COMPLETED | NCT01848184 |
| PARIETEX™ Composite Ventral Patch | Other | Preclinical | Hernia | COMPLETED | NCT01848184 |
| Open, surgical endarterectomy | Other | Approved | Peripheral Artery Disease | UNKNOWN | NCT02517827 |
| Atherectomy and paclitaxel-coated balloon angioplasty | Other | Approved | Peripheral Artery Disease | UNKNOWN | NCT02517827 |
| Sitagliptin and insulin/novolog via CL | Other | Phase PHASE1 | Diabetes Mellitus, Type 1 | COMPLETED | NCT02328040 |
| Placebo and Insulin monotherapy via CL | Drug | Phase PHASE1 | Diabetes Mellitus, Type 1 | COMPLETED | NCT02328040 |
| Transvenous hypoglossal nerve stimulation | Other | Approved | Sleep Apnea, Obstructive | COMPLETED | NCT03210142 |
| Transvenous hypoglossal nerve stimulation | Other | Approved | Sleep Apnea, Obstructive | COMPLETED | NCT03210142 |
| Closed loop with sensor, Insulin and Liraglutide | Other | Phase PHASE2 | Type 1 Diabetes | COMPLETED | NCT01755416 |
| Closed loop with sensor and Insulin | Other | Phase PHASE2 | Type 1 Diabetes | COMPLETED | NCT01755416 |
| Policy Change | Other | Approved | Emergency | COMPLETED | NCT02901197 |
| Education and Reminder Posters | Other | Approved | Emergency | COMPLETED | NCT02901197 |
| Policy Change | Other | Approved | Emergency | COMPLETED | NCT02901197 |
| Education and Reminder Posters | Other | Approved | Emergency | COMPLETED | NCT02901197 |
| The CoreValve™ Evolut R TAV™ system | Other | Approved | Aortic Stenosis | COMPLETED | NCT01876420 |
| Control LVAD | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01166347 |
| HeartWare® VAS | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01166347 |
| Control LVAD | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01166347 |
| HeartWare® VAS | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01166347 |
| Autogenous bone graft from tibia or iliac crest | Other | Approved | Alveolar Bone Loss in Mandible | WITHDRAWN | NCT01308996 |
| INFUSE® Bone Graft | Other | Approved | Alveolar Bone Loss in Mandible | WITHDRAWN | NCT01308996 |
| Autogenous bone graft from tibia or iliac crest | Other | Approved | Alveolar Bone Loss in Mandible | WITHDRAWN | NCT01308996 |
| INFUSE® Bone Graft | Other | Approved | Alveolar Bone Loss in Mandible | WITHDRAWN | NCT01308996 |
| TELAMON P™ /INFUSE® Bone Graft/CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491516 |
| TELAMON P™ /INFUSE® Bone Graft/CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491516 |
| Medtronic Engager Transcatheter Aortic Valve Implantation System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01348438 |
| Medtronic Engager Transcatheter Aortic Valve Implantation System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01348438 |
| Ablation / MRI | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01767558 |
| Ablation / MRI | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01767558 |
| CoreValve aortic valve | Other | Preclinical | Aortic Stenosis | COMPLETED | NCT01676727 |
| CoreValve aortic valve | Other | Preclinical | Aortic Stenosis | COMPLETED | NCT01676727 |
| Arctic Front Advance Cardiac CryoAblation system | Other | Phase PHASE4 | Paroxysmal Atrial Fibrillation | COMPLETED | NCT01645917 |
| Arctic Front Advance Cardiac CryoAblation system | Other | Phase PHASE4 | Paroxysmal Atrial Fibrillation | COMPLETED | NCT01645917 |
| Arctic Front Advance Cardiac CryoAblation system | Other | Phase PHASE4 | Paroxysmal Atrial Fibrillation | COMPLETED | NCT01645917 |
| Ablation procedure and/or cardioversion | Procedure | Phase PHASE1 | Atrial Fibrillation | COMPLETED | NCT00744835 |
| Ablation procedure and/or cardioversion | Procedure | Phase PHASE1 | Atrial Fibrillation | COMPLETED | NCT00744835 |
| Deep Brain Stimulation | Other | Approved | Parkinsons Disease | COMPLETED | NCT02318927 |
| Exilis Implantable Gastric Electrical Stimulation (GES) | Other | Approved | Obesity | COMPLETED | NCT01823705 |
| Exilis Implantable Gastric Electrical Stimulation (GES) | Other | Approved | Obesity | COMPLETED | NCT01823705 |
| Exilis Implantable Gastric Electrical Stimulation (GES) | Other | Approved | Obesity | COMPLETED | NCT01823705 |
| Glipizide | Other | Approved | Chronic Kidney Diseases | COMPLETED | NCT02608177 |
| Linagliptin | Other | Approved | Chronic Kidney Diseases | COMPLETED | NCT02608177 |
| Kerlix AMD gauze | Other | Approved | Burns | COMPLETED | NCT00656708 |
| Kerlix AMD gauze | Other | Approved | Burns | COMPLETED | NCT00656708 |
| Magnetic Resonance Imaging (MRI) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01520532 |
| Echo | Other | Approved | Heart Failure | COMPLETED | NCT00980057 |
| Adaptive CRT (aCRT) | Other | Approved | Heart Failure | COMPLETED | NCT00980057 |
| Echo | Other | Approved | Heart Failure | COMPLETED | NCT00980057 |
| Adaptive CRT (aCRT) | Other | Approved | Heart Failure | COMPLETED | NCT00980057 |
| Freezor® Cardiac Cryoablation Catheter CryoConsole System | Other | Phase PHASE4 | Tachycardia, Atrioventricular Nodal Reentry | COMPLETED | NCT00621621 |
| Freezor® Cardiac Cryoablation Catheter CryoConsole System | Other | Phase PHASE4 | Tachycardia, Atrioventricular Nodal Reentry | COMPLETED | NCT00621621 |
| Class I or III Antiarrhythmic Medications | Drug | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00514735 |
| Medtronic Cardiac Ablation System | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00514735 |
| Class I or III Antiarrhythmic Medications | Drug | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00514735 |
| Medtronic Cardiac Ablation System | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00514735 |
| The AXIUM Progressive Coil System | Other | Preclinical | Aneurysms | COMPLETED | NCT00703794 |
| The AXIUM Progressive Coil System | Other | Preclinical | Aneurysms | COMPLETED | NCT00703794 |
| Desaturation | Other | Approved | Oxygen Deficiency | COMPLETED | NCT03128372 |
| Desaturation | Other | Approved | Oxygen Deficiency | COMPLETED | NCT03128372 |
| McGrath MAC enhanced direct laryngoscope | Other | Approved | Intubation; Difficult | COMPLETED | NCT02250521 |
| McGrath MAC enhanced direct laryngoscope | Other | Approved | Intubation; Difficult | COMPLETED | NCT02250521 |
| McGrath MAC enhanced direct laryngoscope | Other | Approved | Intubation; Difficult | COMPLETED | NCT02250521 |
| Manometry | Other | Approved | Children | UNKNOWN | NCT02812836 |
| High-resolution anorectal manometry | Other | Approved | Constipation | UNKNOWN | NCT02812823 |
| 3D high resolution anorectal manometry | Other | Approved | Children | COMPLETED | NCT02296008 |
| therapy regimen | Drug | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT01995539 |
| Conservative care | Other | Approved | Lumbar Degenerative Disc Disease | TERMINATED | NCT00456378 |
| DIAM™ Spinal Stabilization System | Other | Approved | Lumbar Degenerative Disc Disease | TERMINATED | NCT00456378 |
| Conservative care | Other | Approved | Lumbar Degenerative Disc Disease | TERMINATED | NCT00456378 |
| DIAM™ Spinal Stabilization System | Other | Approved | Lumbar Degenerative Disc Disease | TERMINATED | NCT00456378 |
| Cryoballoon Pulmonary Vein Isolation - PVI | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03786822 |
| MAST™ procedure | Procedure | Preclinical | Degenerative Lumbar Spine Causing Back and/or Leg Pain | COMPLETED | NCT01143324 |
| MAST™ procedure | Procedure | Preclinical | Degenerative Lumbar Spine Causing Back and/or Leg Pain | COMPLETED | NCT01143324 |
| MAST™ procedure | Procedure | Preclinical | Degenerative Lumbar Spine Causing Back and/or Leg Pain | COMPLETED | NCT01143324 |
| NURO System PTNM Therapy | Drug | Approved | Overactive Bladder | COMPLETED | NCT02857816 |
| NURO System PTNM Therapy | Drug | Approved | Overactive Bladder | COMPLETED | NCT02857816 |
| Dual-monitoring | Other | Approved | Cognitive Dysfunction | UNKNOWN | NCT03036345 |
| Medtronic CoreValve System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01051310 |
| Medtronic CoreValve System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01051310 |
| InterStim Therapy | Drug | Approved | Neurogenic Overactive Bladder | TERMINATED | NCT01023269 |
| InterStim Therapy | Drug | Approved | Neurogenic Overactive Bladder | TERMINATED | NCT01023269 |
| Out of cathlab insertion | Other | Approved | Arrhythmia | COMPLETED | NCT02412488 |
| Out of cathlab insertion | Other | Approved | Arrhythmia | COMPLETED | NCT02412488 |
| Pacing Lead (Model 4296 LV Lead) | Other | Approved | Heart Failure | COMPLETED | NCT00927251 |
| Pacing Lead (Model 4296 LV Lead) | Other | Approved | Heart Failure | COMPLETED | NCT00927251 |
| Pacing Lead (Model 4296 LV Lead) | Other | Approved | Heart Failure | COMPLETED | NCT00927251 |
| Pacing Lead | Other | Approved | Heart Failure | COMPLETED | NCT00853593 |
| Pacing Lead | Other | Approved | Heart Failure | COMPLETED | NCT00853593 |
| Pacing Lead | Other | Approved | Heart Failure | COMPLETED | NCT00853593 |
| PROTÉGÉ® EverFlex™ Self-Expanding Stent System | Other | Approved | Peripheral Vascular Diseases | COMPLETED | NCT00530712 |
| PROTÉGÉ® EverFlex™ Self-Expanding Stent System | Other | Approved | Peripheral Vascular Diseases | COMPLETED | NCT00530712 |
| Medtronic CoreValve System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01051518 |
| Medtronic CoreValve System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01051518 |
| Medtronic CoreValve System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01051518 |
| Cardiac Pacing and Impedance Measurement system | Other | Approved | Heart Failure | UNKNOWN | NCT03087084 |
| Cardiac Pacing and Impedance Measurement system | Other | Approved | Heart Failure | UNKNOWN | NCT03087084 |
| tonsillar dissection | Other | Phase PHASE4 | Tonsillar Hypertrophy, Tonsillitis | UNKNOWN | NCT03854279 |
| Successful reperfusion | Other | Preclinical | Ischemic Stroke | COMPLETED | NCT03496064 |
| Hybrid Closed Loop | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01857973 |
| Hybrid Closed Loop | Other | Approved | Type 1 Diabetes | COMPLETED | NCT01857973 |
| EverFlex™ stent with Entrust™ delivery system | Other | Approved | Peripheral Arterial Diseases | COMPLETED | NCT02066740 |
| EverFlex™ stent with Entrust™ delivery system | Other | Approved | Peripheral Arterial Diseases | COMPLETED | NCT02066740 |
| EverFlex™ stent with Entrust™ delivery system | Other | Approved | Peripheral Arterial Diseases | COMPLETED | NCT02066740 |
| Covidien OneShot™ System | Other | Approved | Hypertension, Resistant to Conventional Therapy | COMPLETED | NCT01520506 |
| Covidien OneShot™ System | Other | Approved | Hypertension, Resistant to Conventional Therapy | COMPLETED | NCT01520506 |
| Medtronic MiniMed 530G Insulin Pump | Other | Approved | Diabetes | COMPLETED | NCT02003898 |
| Medtronic MiniMed 530G Insulin Pump | Other | Approved | Diabetes | COMPLETED | NCT02003898 |
| PROTÉGÉ™ GPS™ and PROTÉGÉ™ RX Carotid Stent Systems and SpiderFX™ Embolic Protection Device | Device | Approved | Carotid Artery Disease | COMPLETED | NCT00530504 |
| PROTÉGÉ™ GPS™ and PROTÉGÉ™ RX Carotid Stent Systems and SpiderFX™ Embolic Protection Device | Device | Approved | Carotid Artery Disease | COMPLETED | NCT00530504 |
| Investigational Software loaded on Micra device | Device | Approved | Bradyarrhythmia | COMPLETED | NCT02930980 |
| Investigational Software loaded on Micra device | Device | Approved | Bradyarrhythmia | COMPLETED | NCT02930980 |
| SMBG only | Other | Approved | Diabetes Mellitus | COMPLETED | NCT00111228 |
| Guardian RT | Other | Approved | Diabetes Mellitus | COMPLETED | NCT00111228 |
| SMBG only | Other | Approved | Diabetes Mellitus | COMPLETED | NCT00111228 |
| Guardian RT | Other | Approved | Diabetes Mellitus | COMPLETED | NCT00111228 |
| Resolute Onyx Stent - 2.25 mm - 4.0 mm | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02419521 |
| Resolute Onyx Stent - 2.25 mm - 4.0 mm | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02419521 |
| Standard of Care alone (clinical assessment) | Other | Approved | Congestive Heart Failure | TERMINATED | NCT00510198 |
| Cardiac Compass with OptiVol Fluid Status Monitoring | Other | Approved | Congestive Heart Failure | TERMINATED | NCT00510198 |
| Standard of Care alone (clinical assessment) | Other | Approved | Congestive Heart Failure | TERMINATED | NCT00510198 |
| Cardiac Compass with OptiVol Fluid Status Monitoring | Other | Approved | Congestive Heart Failure | TERMINATED | NCT00510198 |
| complex carbohydrate drink | Other | Approved | Laparoscopic Abdominal Surgery | COMPLETED | NCT02673502 |
| simple carbohydrate drink | Other | Approved | Laparoscopic Abdominal Surgery | COMPLETED | NCT02673502 |
| complex carbohydrate drink | Other | Approved | Laparoscopic Abdominal Surgery | COMPLETED | NCT02673502 |
| simple carbohydrate drink | Other | Approved | Laparoscopic Abdominal Surgery | COMPLETED | NCT02673502 |
| Reveal LINQ ICM Cardiac Monitor, taped on the subject's chest rather than inserted in the body. | Other | Approved | Heart Failure | COMPLETED | NCT02943941 |
| Reveal LINQ ICM Cardiac Monitor, taped on the subject's chest rather than inserted in the body. | Other | Approved | Heart Failure | COMPLETED | NCT02943941 |
| Reveal LINQ ICM Cardiac Monitor, taped on the subject's chest rather than inserted in the body. | Other | Approved | Heart Failure | COMPLETED | NCT02943941 |
| Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02463097 |
| Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02463097 |
| CoreValve Transcatheter Valve | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02209298 |
| CoreValve Transcatheter Valve | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02209298 |
| CoreValve Transcatheter Valve | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02209298 |
| Atherectomy Catheter | Other | Approved | Peripheral Arterial Disease | COMPLETED | NCT02169921 |
| Atherectomy Catheter | Other | Approved | Peripheral Arterial Disease | COMPLETED | NCT02169921 |
| fMRI | Other | Approved | Failed Back Surgery Syndrome | COMPLETED | NCT02650349 |
| Apollo™ Onyx™ Delivery Micro Catheter | Other | Approved | Arteriovenous Malformations | COMPLETED | NCT02378883 |
| Apollo™ Onyx™ Delivery Micro Catheter | Other | Approved | Arteriovenous Malformations | COMPLETED | NCT02378883 |
| Resolute Integrity Stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01913600 |
| Resolute Integrity Stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01913600 |
| Telemetry Monitoring | Other | Approved | Telemetry | TERMINATED | NCT03039738 |
| Vital Sync IM & VPMP (Surveillance Monitoring) | Other | Approved | Telemetry | TERMINATED | NCT03039738 |
| Telemetry Monitoring | Other | Approved | Telemetry | TERMINATED | NCT03039738 |
| Vital Sync IM & VPMP (Surveillance Monitoring) | Other | Approved | Telemetry | TERMINATED | NCT03039738 |
| Intact Breast Lesion Excision System (BLES) | Other | Preclinical | Breast Lesions | TERMINATED | NCT03520127 |
| Intact Breast Lesion Excision System (BLES) | Other | Preclinical | Breast Lesions | TERMINATED | NCT03520127 |
| Near-InfraRed Spectroscopy (NIRS) | Other | Preclinical | Liver Failure | TERMINATED | NCT02343016 |
| Near-InfraRed Spectroscopy (NIRS) | Other | Preclinical | Liver Failure | TERMINATED | NCT02343016 |
| Near-InfraRed Spectroscopy (NIRS) | Other | Preclinical | Liver Failure | TERMINATED | NCT02343016 |
| Upper Limit of Vulnerability Testing | Other | Approved | Cardiomyopathy | COMPLETED | NCT02111993 |
| Standard Defibrillation Testing | Other | Approved | Cardiomyopathy | COMPLETED | NCT02111993 |
| Ablation with cryoenergy | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03960346 |
| TurboHawk/SilverHawk + Cotavance Drug-Eluting Balloon | Drug | Approved | Peripheral Arterial Disease | COMPLETED | NCT01366482 |
| Cotavance Drug-Eluting Balloon | Drug | Approved | Peripheral Arterial Disease | COMPLETED | NCT01366482 |
| TurboHawk/SilverHawk + Cotavance Drug-Eluting Balloon | Drug | Approved | Peripheral Arterial Disease | COMPLETED | NCT01366482 |
| Cotavance Drug-Eluting Balloon | Drug | Approved | Peripheral Arterial Disease | COMPLETED | NCT01366482 |
| Implant of an MR-conditional Tachy device system | Device | Preclinical | Tachyarrhythmia | COMPLETED | NCT02849769 |
| EUS-FNA needle (Beacon) | Other | Approved | Pancreas Cancer | COMPLETED | NCT03532347 |
| Capnostream Monitor | Other | Approved | Respiratory Depression | COMPLETED | NCT02811302 |
| Capnostream Monitor | Other | Approved | Respiratory Depression | COMPLETED | NCT02811302 |
| Endocardial Left Ventricular pacing | Other | Approved | Heart Failure | COMPLETED | NCT01277783 |
| Endocardial Left Ventricular pacing | Other | Approved | Heart Failure | COMPLETED | NCT01277783 |
| Atorvastatin Placebo | Other | Phase PHASE3 | Diabetes Mellitus, Insulin-Dependent | COMPLETED | NCT01236365 |
| Atorvastatin | Other | Phase PHASE3 | Diabetes Mellitus, Insulin-Dependent | COMPLETED | NCT01236365 |
| Resolute Onyx Stent - 2.0 mm | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02412501 |
| Resolute Onyx Stent - 2.0 mm | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02412501 |
| HeartWare® VAS | Other | Preclinical | Heart Failure | COMPLETED | NCT01832610 |
| HeartWare® VAS | Other | Preclinical | Heart Failure | COMPLETED | NCT01832610 |
| Cryoballoon Ablation: PVI + substrate modification | Other | Approved | Atrial Fibrillation | WITHDRAWN | NCT03489096 |
| Bravo pH monitoring procedure | Procedure | Approved | Gastro Esophageal Reflux Disease | WITHDRAWN | NCT01788085 |
| Bravo pH monitoring procedure | Procedure | Approved | Gastro Esophageal Reflux Disease | WITHDRAWN | NCT01788085 |
| The preparation regimen | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT01575093 |
| The preparation regimen | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT01575093 |
| Bravo® pH Monitoring System | Other | Phase PHASE4 | Gastro Esophageal Reflux Disease | COMPLETED | NCT01503476 |
| Bravo® pH Monitoring System | Other | Phase PHASE4 | Gastro Esophageal Reflux Disease | COMPLETED | NCT01503476 |
| PillCam® capsule with Given PillCam® Platform | Other | Phase PHASE1 | Upper GI Bleeding | TERMINATED | NCT01448382 |
| PillCam® capsule with Given PillCam® Platform | Other | Phase PHASE1 | Upper GI Bleeding | TERMINATED | NCT01448382 |
| Cleaning capsule | Other | Phase PHASE1 | Healthy | TERMINATED | NCT01370759 |
| Cleaning capsule | Other | Phase PHASE1 | Healthy | TERMINATED | NCT01370759 |
| PillCam™ (Capsule Endoscopy) Colon 2 capsule | Other | Phase PHASE3 | Colonic Diseases | COMPLETED | NCT01063231 |
| Capsule Endoscopy | Other | Preclinical | Celiac Disease | COMPLETED | NCT00555737 |
| Capsule Endoscopy | Other | Preclinical | Celiac Disease | COMPLETED | NCT00555737 |
| PillCam Colon capsule endoscopy | Other | Preclinical | Colonic Diseases | TERMINATED | NCT00440791 |
| PillCam Colon capsule endoscopy | Other | Preclinical | Colonic Diseases | TERMINATED | NCT00440791 |
| PillCam Colon capsule endoscopy | Other | Preclinical | Colonic Diseases | TERMINATED | NCT00440791 |
| Ileocolonoscopy | Other | Phase PHASE1 | Crohn's Disease | COMPLETED | NCT01631435 |
| Pillcam colon capsule and PillCam™ Prep Procedure | Procedure | Phase PHASE1 | Crohn's Disease | COMPLETED | NCT01631435 |
| Ileocolonoscopy | Other | Phase PHASE1 | Crohn's Disease | COMPLETED | NCT01631435 |
| Pillcam colon capsule and PillCam™ Prep Procedure | Procedure | Phase PHASE1 | Crohn's Disease | COMPLETED | NCT01631435 |
| capsule endoscopy | Other | Approved | Small/Large Bowel | COMPLETED | NCT01433042 |
| capsule endoscopy | Other | Approved | Small/Large Bowel | COMPLETED | NCT01433042 |
| Colonoscopy | Other | Approved | CRC Screening | COMPLETED | NCT01372878 |
| PillCam® COLON 2 procedure | Procedure | Approved | CRC Screening | COMPLETED | NCT01372878 |
| Colonoscopy | Other | Approved | CRC Screening | COMPLETED | NCT01372878 |
| PillCam® COLON 2 procedure | Procedure | Approved | CRC Screening | COMPLETED | NCT01372878 |
| Standard colonoscopy | Other | Phase PHASE3 | Colonic Diseases | COMPLETED | NCT00604162 |
| PillCam COLON | Other | Phase PHASE3 | Colonic Diseases | COMPLETED | NCT00604162 |
| Standard colonoscopy | Other | Phase PHASE3 | Colonic Diseases | COMPLETED | NCT00604162 |
| PillCam COLON | Other | Phase PHASE3 | Colonic Diseases | COMPLETED | NCT00604162 |
| CRT pacing at rest and during exercise | Other | Approved | Heart Failure | TERMINATED | NCT01475175 |
| CRT pacing at rest and during exercise | Other | Approved | Heart Failure | TERMINATED | NCT01475175 |
| Placebo | Other | Approved | Neuropathic Pain | COMPLETED | NCT02705950 |
| Intrathecal baclofen bolus | Other | Approved | Neuropathic Pain | COMPLETED | NCT02705950 |
| Enlite 1 connected to iPro2 recorder | Other | Approved | Diabetes Mellitus | COMPLETED | NCT03417466 |
| Enlite 1 connected to iPro2 recorder | Other | Approved | Diabetes Mellitus | COMPLETED | NCT03417466 |
| External Loop Recorder | Other | Approved | Post MI Left Ventricular Dysfunction | COMPLETED | NCT01995552 |
| SAP+PLGM | Other | Approved | Type1diabetes | UNKNOWN | NCT04073576 |
| AHCL | Other | Approved | Type1diabetes | UNKNOWN | NCT04073576 |
| ICD implantation | Other | Preclinical | Myocardial Infarction | COMPLETED | NCT02124018 |
| Programmed ventricular stimulation | Other | Preclinical | Myocardial Infarction | COMPLETED | NCT02124018 |
| Implant of the HW005 Ventricular Assist System. | Other | Approved | Heart Failure | COMPLETED | NCT02091440 |
| Implant of the HW005 Ventricular Assist System. | Other | Approved | Heart Failure | COMPLETED | NCT02091440 |
| Implant of the HW005 Ventricular Assist System. | Other | Approved | Heart Failure | COMPLETED | NCT02091440 |
| insulin pump and blinded continuous glucose sensing (Paradigm Real-Time insulin pump) | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT00598663 |
| insulin pump with continuous glucose sensing (Paradigm Real-Time Insulin Pump System) | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT00598663 |
| insulin pump and blinded continuous glucose sensing (Paradigm Real-Time insulin pump) | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT00598663 |
| insulin pump with continuous glucose sensing (Paradigm Real-Time Insulin Pump System) | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT00598663 |
| Medtronic Coronary Drug-Coated Balloon Catheter | Drug | Approved | In-stent Restenosis | COMPLETED | NCT03260517 |
| Medtronic Coronary Drug-Coated Balloon Catheter | Drug | Approved | In-stent Restenosis | COMPLETED | NCT03260517 |
| Computed Tomographic Colonography | Other | Approved | Colorectal Cancer Screening | COMPLETED | NCT02754661 |
| COLON Capsule endoscopy | Other | Approved | Colorectal Cancer Screening | COMPLETED | NCT02754661 |
| Computed Tomographic Colonography | Other | Approved | Colorectal Cancer Screening | COMPLETED | NCT02754661 |
| COLON Capsule endoscopy | Other | Approved | Colorectal Cancer Screening | COMPLETED | NCT02754661 |
| Chart review | Other | Preclinical | Varicose Veins | COMPLETED | NCT04006184 |
| Seated Control | Other | Approved | Walking | COMPLETED | NCT02834689 |
| Walking | Other | Approved | Walking | COMPLETED | NCT02834689 |
| Cardiac resynchronization therapy | Drug | Preclinical | Cardiac Resynchronization Therapy, Non-LBBB, QRS Area | UNKNOWN | NCT04120909 |
| ReliaTack™ Articulating Reloadable Fixation Device | Device | Preclinical | Inguinal Hernia | COMPLETED | NCT03526341 |
| ReliaTack™ Articulating Reloadable Fixation Device | Device | Preclinical | Inguinal Hernia | COMPLETED | NCT03526341 |
| external drug infusion pump | Drug | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| ribavirin, USP | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| peginterferon alfa-2b | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| interferon alfa-2b | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| external drug infusion pump | Drug | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| ribavirin, USP | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| peginterferon alfa-2b | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| interferon alfa-2b | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT00919633 |
| Medtronic endoscope | Other | Approved | Coronary Bypass Stenosis | COMPLETED | NCT04127461 |
| MDT-2111 TAVI 23 mm | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01634269 |
| MDT-2111 TAVI 23 mm | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01634269 |
| Continuous Glucose Monitoring (CGM) | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT04141111 |
| Ultrasound | Other | Preclinical | Varicose Veins | UNKNOWN | NCT04146168 |
| Ultrasound | Other | Preclinical | Varicose Veins | UNKNOWN | NCT04146168 |
| Ultrasound | Other | Preclinical | Varicose Veins | UNKNOWN | NCT04146168 |
| Pulmonary vein ablation | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT03242941 |
| Pulmonary vein ablation | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT03242941 |
| Melody Transcatheter Pulmonary Valve PB1016 | Other | Approved | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | COMPLETED | NCT02347189 |
| Melody Transcatheter Pulmonary Valve PB1016 | Other | Approved | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | COMPLETED | NCT02347189 |
| Melody Transcatheter Pulmonary Valve PB1016 | Other | Approved | Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects | COMPLETED | NCT02347189 |
| Reveal LINQ™ Insertable Cardiac Monitor (ICM) | Other | Preclinical | Heart Failure | COMPLETED | NCT02758301 |
| No treatment | Drug | Preclinical | Lead Insulation Failure | TERMINATED | NCT02314598 |
| No treatment | Drug | Preclinical | Lead Insulation Failure | TERMINATED | NCT02314598 |
| Medtronic CoreValve® System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01015612 |
| Medtronic CoreValve® System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT01015612 |
| EndoFLIP™ System with FLIP Topography Module | Other | Approved | Healthy Subjects | WITHDRAWN | NCT03831724 |
| EndoFLIP™ System with FLIP Topography Module | Other | Approved | Healthy Subjects | WITHDRAWN | NCT03831724 |
| Continuous glucose monitoring | Other | Preclinical | Continuous Glucose Monitoring | UNKNOWN | NCT04172116 |
| Ugytex | Other | Approved | Vaginal Prolapse | COMPLETED | NCT00153257 |
| Ugytex | Other | Approved | Vaginal Prolapse | COMPLETED | NCT00153257 |
| No Intervention | Other | Preclinical | Abdominal Aortic Aneurysm | UNKNOWN | NCT02604303 |
| Thoracotomy | Other | Approved | Left Sided Heart Failure | COMPLETED | NCT02268942 |
| HeartWare HVAD | Other | Approved | Left Sided Heart Failure | COMPLETED | NCT02268942 |
| Thoracotomy | Other | Approved | Left Sided Heart Failure | COMPLETED | NCT02268942 |
| HeartWare HVAD | Other | Approved | Left Sided Heart Failure | COMPLETED | NCT02268942 |
| EverFlex™ Self-Expanding Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | COMPLETED | NCT01680835 |
| EverFlex™ Self-Expanding Peripheral Stent System | Other | Approved | Peripheral Arterial Disease | COMPLETED | NCT01680835 |
| Pipeline™ Embolization Device/ Pipeline™Flex Embolization Device | Device | Approved | Intracranial Aneurysm | COMPLETED | NCT02186561 |
| Pipeline™ Embolization Device/ Pipeline™Flex Embolization Device | Device | Approved | Intracranial Aneurysm | COMPLETED | NCT02186561 |
| Diagnostic & Medication Management | Drug | Approved | Heart Failure | TERMINATED | NCT02698241 |
| Diagnostic & Medication Management | Drug | Approved | Heart Failure | TERMINATED | NCT02698241 |
| Diagnostic & Medication Management | Drug | Approved | Heart Failure | TERMINATED | NCT02698241 |
| HLCL- Hybrid Logic Closed Loop System | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02651181 |
| Fine Needle Aspiration (FNA) | Other | Approved | Pancreatic Cancer | COMPLETED | NCT02678442 |
| Fine Needle Biopsy (FNB) | Other | Approved | Pancreatic Cancer | COMPLETED | NCT02678442 |
| SubQ | Other | Approved | Low Back Pain | COMPLETED | NCT01776749 |
| Attain Stability Quad Left Ventricular Pacing Lead | Other | Approved | Heart Failure | COMPLETED | NCT03099655 |
| Attain Stability Quad Left Ventricular Pacing Lead | Other | Approved | Heart Failure | COMPLETED | NCT03099655 |
| Facial Nerve Monitor | Other | Approved | Parotid Gland Disorders | TERMINATED | NCT03172520 |
| APS electrode | Other | Approved | Parotid Gland Disorders | TERMINATED | NCT03172520 |
| MiniMed™640G | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02733991 |
| MiniMed™640G and Suspend before low | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02733991 |
| MiniMed™640G | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02733991 |
| MiniMed™640G and Suspend before low | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02733991 |
| MiniMed™640G | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02733991 |
| MiniMed™640G and Suspend before low | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02733991 |
| Chronotropic Incompetence Diagnostic Algorithm | Other | Approved | Heart Failure | TERMINATED | NCT02358603 |
| Chronotropic Incompetence Diagnostic Algorithm | Other | Approved | Heart Failure | TERMINATED | NCT02358603 |
| Medtronic Adapta Dual Chamber Pacemaker | Other | Approved | Bradycardia | COMPLETED | NCT01039467 |
| Medtronic Adapta Dual Chamber Pacemaker | Other | Approved | Bradycardia | COMPLETED | NCT01039467 |
| CRT with LV-only pacing / bi-ventricular pacing | Other | Approved | Heart Failure | COMPLETED | NCT03071978 |
| CRT with LV-only pacing / bi-ventricular pacing | Other | Approved | Heart Failure | COMPLETED | NCT03071978 |
| Ibutilide | Other | Approved | Atrial Fibrillation | TERMINATED | NCT03370536 |
| AF ablation | Other | Approved | Atrial Fibrillation | TERMINATED | NCT03370536 |
| CardioInsight ECGI Mapping System | Other | Approved | Atrial Fibrillation | TERMINATED | NCT03370536 |
| Use of the Achieve catheter followed by ICE-guided mapping catheter | Other | Approved | Atrial Fibrillation | COMPLETED | NCT01772030 |
| Stentriever Solitaire FR® or Penumbra System® | Other | Phase PHASE3 | Stroke | COMPLETED | NCT02216643 |
| Thrombectomy | Other | Phase PHASE3 | Stroke | COMPLETED | NCT02216643 |
| Pacemaker stimulation mode | Other | Approved | Diastolic Function | COMPLETED | NCT04068233 |
| Percutaneous device closure | Device | Preclinical | Cryptogenic Stroke | UNKNOWN | NCT04285918 |
| Aquamantys System | Other | Approved | Infection of Total Knee Joint Prosthesis | COMPLETED | NCT02266407 |
| Aquamantys System | Other | Approved | Infection of Total Knee Joint Prosthesis | COMPLETED | NCT02266407 |
| Bipolar sealer Aquamantys | Other | Approved | Osteoarthritis | COMPLETED | NCT01736644 |
| Electrocautery | Other | Approved | Osteoarthritis | COMPLETED | NCT01736644 |
| Bipolar sealer Aquamantys | Other | Approved | Osteoarthritis | COMPLETED | NCT01736644 |
| Electrocautery | Other | Approved | Osteoarthritis | COMPLETED | NCT01736644 |
| occipital nerve stimulation | Other | Phase PHASE3 | Chronic Cluster Headache | COMPLETED | NCT01151631 |
| CeraFlex | Other | Approved | Patent Foramen Ovale | COMPLETED | NCT02621528 |
| Stimulating the phrenic nerve intravenously using high frequency electrical pulses using an EP catheter connected to external pulse stimulator. | Other | Approved | Sleep Apnea | COMPLETED | NCT01981590 |
| Stimulating the phrenic nerve intravenously using high frequency electrical pulses using an EP catheter connected to external pulse stimulator. | Other | Approved | Sleep Apnea | COMPLETED | NCT01981590 |
| Stimulating the phrenic nerve intravenously using high frequency electrical pulses using an EP catheter connected to external pulse stimulator. | Other | Approved | Sleep Apnea | COMPLETED | NCT01981590 |
| 3D accelerometer | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Reveal LINQ accelerometer | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-Expanded Timed Get-Up-and-Go (ETGUG) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-Five Times Sit to Stand (FTSTS) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-4 Meter Gait Speed (4MGS) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-Six Minute Walk (6MW) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| 3D accelerometer | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Reveal LINQ accelerometer | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-Expanded Timed Get-Up-and-Go (ETGUG) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-Five Times Sit to Stand (FTSTS) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-4 Meter Gait Speed (4MGS) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| Walking Exercises-Six Minute Walk (6MW) Test | Other | Approved | Heart Failure | COMPLETED | NCT02755129 |
| A bipolar instrument for tonsillectomies | Device | Approved | Tonsillectomy | COMPLETED | NCT02876575 |
| A bipolar instrument for tonsillectomies | Device | Approved | Tonsillectomy | COMPLETED | NCT02876575 |
| A bipolar instrument for tonsillectomies | Device | Approved | Tonsillectomy | COMPLETED | NCT02876575 |
| NIRS monitoring | Other | Preclinical | Intraventricular Hemorrhage of Prematurity | COMPLETED | NCT02147769 |
| NIRS monitoring | Other | Preclinical | Intraventricular Hemorrhage of Prematurity | COMPLETED | NCT02147769 |
| Spinal Cord Stimulation | Other | Phase PHASE4 | Back Pain | COMPLETED | NCT03284411 |
| Spinal Cord Stimulation | Other | Phase PHASE4 | Back Pain | COMPLETED | NCT03284411 |
| PEAK PlasmaBlade™ | Other | Approved | Breast Reconstruction | COMPLETED | NCT04350411 |
| Conventional diathermy | Other | Approved | Breast Reconstruction | COMPLETED | NCT04350411 |
| lumbar corset | Other | Phase PHASE3 | Lumbar Fusion | COMPLETED | NCT00620399 |
| lumbar corset | Other | Phase PHASE3 | Lumbar Fusion | COMPLETED | NCT00620399 |
| lumbar corset | Other | Phase PHASE3 | Lumbar Fusion | COMPLETED | NCT00620399 |
| Medtronic CoreValve™ Evolut R™ System | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02592369 |
| Medtronic CoreValve™ Evolut R™ System | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT02592369 |
| 7 day infusion set | Other | Approved | Type1diabetes | COMPLETED | NCT04208282 |
| BiZact™: A bipolar instrument for tonsillectomies | Device | Approved | Tonsillectomy | COMPLETED | NCT03266094 |
| BiZact™: A bipolar instrument for tonsillectomies | Device | Approved | Tonsillectomy | COMPLETED | NCT03266094 |
| Placebo | Other | Phase PHASE4 | Abdominal Aortic Aneurysm | COMPLETED | NCT01683084 |
| Telmisartan | Other | Phase PHASE4 | Abdominal Aortic Aneurysm | COMPLETED | NCT01683084 |
| MARVEL 2 Algorithm Monitor Mode then Adaptive Mode | Other | Approved | Atrioventricular Conduction Block | COMPLETED | NCT03752151 |
| MARVEL 2 Algorithm Monitor Mode then Adaptive Mode | Other | Approved | Atrioventricular Conduction Block | COMPLETED | NCT03752151 |
| MARVEL 2 Algorithm Monitor Mode then Adaptive Mode | Other | Approved | Atrioventricular Conduction Block | COMPLETED | NCT03752151 |
| Filling in an online survey regarding goalsettings | Other | Preclinical | Chronic Pain | COMPLETED | NCT03938142 |
| Direct laryngoscopy | Other | Approved | Morbid Obesity | COMPLETED | NCT03467048 |
| McGrath videolaryngoscopy | Other | Approved | Morbid Obesity | COMPLETED | NCT03467048 |
| PillCam SB2 | Other | Approved | Intestinal Abnormalities | TERMINATED | NCT01085513 |
| PillCam SB2 | Other | Approved | Intestinal Abnormalities | TERMINATED | NCT01085513 |
| HyGIeaCare colon irrigation | Other | Approved | Screening Colonoscopy | COMPLETED | NCT03458390 |
| Native Outflow Tract TPV | Other | Approved | Congenital Heart Disease | COMPLETED | NCT01762124 |
| Native Outflow Tract TPV | Other | Approved | Congenital Heart Disease | COMPLETED | NCT01762124 |
| Radiofrequency ablation | Other | Approved | Esophageal Squamous Cell Neoplasia (ESCN) | TERMINATED | NCT02953418 |
| Radiofrequency ablation | Other | Approved | Esophageal Squamous Cell Neoplasia (ESCN) | TERMINATED | NCT02953418 |
| Radiofrequency ablation | Other | Approved | Esophageal Squamous Cell Neoplasia (ESCN) | TERMINATED | NCT02953418 |
| Neurothrombectomy | Other | Preclinical | Stroke, Acute | COMPLETED | NCT03364023 |
| Neurothrombectomy | Other | Preclinical | Stroke, Acute | COMPLETED | NCT03364023 |
| Propofol | Other | Phase PHASE4 | Delayed Emergence From Anesthesia | COMPLETED | NCT02631525 |
| Desflurane | Other | Phase PHASE4 | Delayed Emergence From Anesthesia | COMPLETED | NCT02631525 |
| Propofol | Other | Phase PHASE4 | Delayed Emergence From Anesthesia | COMPLETED | NCT02631525 |
| Desflurane | Other | Phase PHASE4 | Delayed Emergence From Anesthesia | COMPLETED | NCT02631525 |
| Valiant Mona LSA Thoracic Stent Graft System | Other | Approved | Aortic Aneurysm, Thoracic | WITHDRAWN | NCT03738124 |
| Valiant Mona LSA Thoracic Stent Graft System | Other | Approved | Aortic Aneurysm, Thoracic | WITHDRAWN | NCT03738124 |
| conventional balloon angioplasty | Other | Phase PHASE4 | Atherosclerosis | UNKNOWN | NCT04539145 |
| Chocolate PTA Balloon | Other | Phase PHASE4 | Atherosclerosis | UNKNOWN | NCT04539145 |
| LV endocardial CRT | Other | Approved | Heart Failure, Left Ventricular Dysfunction | TERMINATED | NCT02757976 |
| Conventional CRT | Other | Approved | Heart Failure, Left Ventricular Dysfunction | TERMINATED | NCT02757976 |
| Sensor wear | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT01161043 |
| Sensor wear | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT01161043 |
| Guardian™ Sensor (3) | Other | Approved | Diabetes Mellitus | COMPLETED | NCT03710083 |
| Guardian™ Sensor (3) | Other | Approved | Diabetes Mellitus | COMPLETED | NCT03710083 |
| Lumbar fusion | Other | Approved | Intervertebral Disc Degeneration | WITHDRAWN | NCT04408846 |
| Guardian Sensor (3) | Other | Approved | Type 1 Diabetes | COMPLETED | NCT04020822 |
| Guardian Sensor (3) | Other | Approved | Type 1 Diabetes | COMPLETED | NCT04020822 |
| Medtronic Activa PC+S | Other | Approved | Spinal Cord Injury | COMPLETED | NCT02564419 |
| Focal Laser Ablation | Other | Phase EARLY_PHASE1 | Prostate Cancer | COMPLETED | NCT02357121 |
| Electrophysiological Study | Other | Approved | Heart Failure | COMPLETED | NCT02914457 |
| Electrophysiological Study | Other | Approved | Heart Failure | COMPLETED | NCT02914457 |
| BIS device | Device | Preclinical | Anesthesia, General | COMPLETED | NCT03553953 |
| BIS device | Device | Preclinical | Anesthesia, General | COMPLETED | NCT03553953 |
| Harmony 1 Sensor | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02456922 |
| Harmony 1 Sensor | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT02456922 |
| Micra Transcatheter Pacing System (TPS) | Other | Approved | Bradycardia | COMPLETED | NCT03624504 |
| Micra Transcatheter Pacing System (TPS) | Other | Approved | Bradycardia | COMPLETED | NCT03624504 |
| Micra Transcatheter Pacing System (TPS) | Other | Approved | Bradycardia | COMPLETED | NCT03624504 |
| IPI | Other | Preclinical | Respiratory Depression | COMPLETED | NCT03050983 |
| IPI | Other | Preclinical | Respiratory Depression | COMPLETED | NCT03050983 |
| Colonoscopy | Other | Approved | Colorectal Lesions | COMPLETED | NCT01269372 |
| PillCam Colon 2 | Other | Approved | Colorectal Lesions | COMPLETED | NCT01269372 |
| Colonoscopy | Other | Approved | Colorectal Lesions | COMPLETED | NCT01269372 |
| PillCam Colon 2 | Other | Approved | Colorectal Lesions | COMPLETED | NCT01269372 |
| TAVR | Other | Preclinical | Symptomatic Aortic Stenosis | COMPLETED | NCT02424370 |
| Nitinol Stent Placement | Other | Approved | Peripheral Vascular Disease | COMPLETED | NCT02850107 |
| Volcano Visions® PV .014" IVUS catheter | Other | Approved | Peripheral Vascular Disease | COMPLETED | NCT02850107 |
| Medtronic Spider™ Distal Protection Device (DPD) | Device | Approved | Peripheral Vascular Disease | COMPLETED | NCT02850107 |
| Medtronic IN.PACT® Admiral® DCB | Other | Approved | Peripheral Vascular Disease | COMPLETED | NCT02850107 |
| Medtronic HawkOne® or TurboHawk™ | Other | Approved | Peripheral Vascular Disease | COMPLETED | NCT02850107 |
| Introduction of Motion conditions: tapping or rubbing | Other | Preclinical | Hypoxia | COMPLETED | NCT04559763 |
| Non-Invasive Controlled Hypoxia | Other | Preclinical | Hypoxia | COMPLETED | NCT04559763 |
| Introduction of Motion conditions: tapping or rubbing | Other | Preclinical | Hypoxia | COMPLETED | NCT04559763 |
| Non-Invasive Controlled Hypoxia | Other | Preclinical | Hypoxia | COMPLETED | NCT04559763 |
| PillCam® Express Capsule Endoscopy Delivery System | Other | Approved | Small Bowel Disease | COMPLETED | NCT01088646 |
| PillCam® Express Capsule Endoscopy Delivery System | Other | Approved | Small Bowel Disease | COMPLETED | NCT01088646 |
| PillCam™ (Capsule Endoscopy) Colon 2 capsule | Other | Approved | Colonic Diseases | COMPLETED | NCT01087528 |
| PillCam™ (Capsule Endoscopy) Colon 2 capsule | Other | Approved | Colonic Diseases | COMPLETED | NCT01087528 |
| Capsule Endoscopy | Other | Approved | Crohn's Disease | COMPLETED | NCT00487396 |
| Capsule Endoscopy | Other | Approved | Crohn's Disease | COMPLETED | NCT00487396 |
| Control LVAD | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01966458 |
| HeartWare® VAS (HVAD) | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01966458 |
| Control LVAD | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01966458 |
| HeartWare® VAS (HVAD) | Other | Approved | Chronic Heart Failure | COMPLETED | NCT01966458 |
| ICD or CRT-D Device | Device | Approved | Sudden Cardiac Arrest | COMPLETED | NCT02099721 |
| ICD or CRT-D Device | Device | Approved | Sudden Cardiac Arrest | COMPLETED | NCT02099721 |
| insulin pump Medtronic 780G | Other | Approved | Diabetes Mellitus, Type 1 | UNKNOWN | NCT04616391 |
| insulin pump Medtronic 780G | Other | Approved | Diabetes Mellitus, Type 1 | UNKNOWN | NCT04616391 |
| Standard settings | Other | Approved | Heart Failure, Systolic | COMPLETED | NCT03220659 |
| Multi-point pacing | Other | Approved | Heart Failure, Systolic | COMPLETED | NCT03220659 |
| Sham procedure | Procedure | Approved | Osteoporosis | COMPLETED | NCT01963039 |
| percutaneous vertebroplasty | Other | Approved | Osteoporosis | COMPLETED | NCT01963039 |
| Medical Ventricular Rate Control | Other | Approved | Heart Failure | COMPLETED | NCT01522898 |
| AV nodal ablation | Other | Approved | Heart Failure | COMPLETED | NCT01522898 |
| Cytosponge | Other | Approved | Barrett's Esophagus | COMPLETED | NCT02106910 |
| Biosensors BioFreedom BA9 Drug Coated Coronary Stent | Drug | Approved | Coronary Artery Disease | COMPLETED | NCT03344653 |
| Medtronic Resolute Onyx Zotarolimus-Eluting Coronary Stent System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT03344653 |
| Biosensors BioFreedom BA9 Drug Coated Coronary Stent | Drug | Approved | Coronary Artery Disease | COMPLETED | NCT03344653 |
| Medtronic Resolute Onyx Zotarolimus-Eluting Coronary Stent System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT03344653 |
| acellular porcine dermal collagen mesh | Other | Phase PHASE2 | Hernia | TERMINATED | NCT00820040 |
| acellular porcine dermal collagen mesh | Other | Phase PHASE2 | Hernia | TERMINATED | NCT00820040 |
| exercises | Other | Approved | COPD | UNKNOWN | NCT04671888 |
| exercises | Other | Approved | COPD | UNKNOWN | NCT04671888 |
| Professional continuous glucose monitoring (CGM) sensor (iPro™2) | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT04667728 |
| Fusion | Other | Phase PHASE3 | Degenerative Lumbar Spinal Stenosis | TERMINATED | NCT00627497 |
| DIAM Spinal Stabilization | Other | Phase PHASE3 | Degenerative Lumbar Spinal Stenosis | TERMINATED | NCT00627497 |
| Single-Level Posterior Decompression | Other | Phase PHASE3 | Degenerative Lumbar Spinal Stenosis | TERMINATED | NCT00627497 |
| Fusion | Other | Phase PHASE3 | Degenerative Lumbar Spinal Stenosis | TERMINATED | NCT00627497 |
| DIAM Spinal Stabilization | Other | Phase PHASE3 | Degenerative Lumbar Spinal Stenosis | TERMINATED | NCT00627497 |
| Single-Level Posterior Decompression | Other | Phase PHASE3 | Degenerative Lumbar Spinal Stenosis | TERMINATED | NCT00627497 |
| provocative discography | Other | Phase PHASE4 | Low Back Pain | COMPLETED | NCT00443781 |
| functional anesthetic discography | Other | Phase PHASE4 | Low Back Pain | COMPLETED | NCT00443781 |
| provocative discography | Other | Phase PHASE4 | Low Back Pain | COMPLETED | NCT00443781 |
| functional anesthetic discography | Other | Phase PHASE4 | Low Back Pain | COMPLETED | NCT00443781 |
| provocative discography | Other | Phase PHASE4 | Low Back Pain | COMPLETED | NCT00443781 |
| functional anesthetic discography | Other | Phase PHASE4 | Low Back Pain | COMPLETED | NCT00443781 |
| Non Surgical Management | Other | Approved | Cancer | COMPLETED | NCT00211237 |
| Balloon Kyphoplasty | Other | Approved | Cancer | COMPLETED | NCT00211237 |
| Non Surgical Management | Other | Approved | Cancer | COMPLETED | NCT00211237 |
| Balloon Kyphoplasty | Other | Approved | Cancer | COMPLETED | NCT00211237 |
| Non Surgical Management | Other | Approved | Cancer | COMPLETED | NCT00211237 |
| Balloon Kyphoplasty | Other | Approved | Cancer | COMPLETED | NCT00211237 |
| Capnography CO2 cannula sampling Flexiterline (CCSF) designs with supplemental O2 | Other | Approved | Capnography | COMPLETED | NCT03554629 |
| Capnography CO2 cannula sampling Flexiterline (CCSF) designs with supplemental O2 | Other | Approved | Capnography | COMPLETED | NCT03554629 |
| InterStim Therapy | Drug | Approved | Urinary Urge Incontinence | COMPLETED | NCT03335761 |
| InterStim Therapy | Drug | Approved | Urinary Urge Incontinence | COMPLETED | NCT03335761 |
| InterStim Therapy | Drug | Approved | Urinary Urge Incontinence | COMPLETED | NCT03335761 |
| DiamondTemp Cardiac Ablation System | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03626649 |
| DiamondTemp Cardiac Ablation System | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03626649 |
| LMWH | Other | Approved | Venous Thromboembolism | COMPLETED | NCT03044574 |
| GCS | Other | Approved | Venous Thromboembolism | COMPLETED | NCT03044574 |
| SCD | Other | Approved | Venous Thromboembolism | COMPLETED | NCT03044574 |
| Percutaneous creation of an arteriovenous fistula | Other | Approved | Renal Insufficiency, Chronic | COMPLETED | NCT02816398 |
| Percutaneous creation of an arteriovenous fistula | Other | Approved | Renal Insufficiency, Chronic | COMPLETED | NCT02816398 |
| Ellipsys Vascular Access | Other | Preclinical | End-stage Renal Disease | COMPLETED | NCT03454113 |
| Ellipsys Vascular Access | Other | Preclinical | End-stage Renal Disease | COMPLETED | NCT03454113 |
| Ellipsys Vascular Access | Other | Preclinical | End-stage Renal Disease | COMPLETED | NCT03454113 |
| REVEAL Insertable Cardiac Monitor (ICM) | Other | Approved | End Stage Renal Disease | COMPLETED | NCT01779856 |
| REVEAL Insertable Cardiac Monitor (ICM) | Other | Approved | End Stage Renal Disease | COMPLETED | NCT01779856 |
| Cardiac Resynchronization Therapy - MPP | Drug | Preclinical | Heart Failure | COMPLETED | NCT03232944 |
| Pulse Oximetry | Other | Preclinical | Respiratory Complications | COMPLETED | NCT02729077 |
| Pulse Oximetry | Other | Preclinical | Respiratory Complications | COMPLETED | NCT02729077 |
| Pulse Oximetry | Other | Preclinical | Respiratory Complications | COMPLETED | NCT02729077 |
| Lymphadenectomy | Other | Approved | Lung Neoplasm Malignant | UNKNOWN | NCT04778826 |
| Lymphadenectomy | Other | Approved | Lung Neoplasm Malignant | UNKNOWN | NCT04778826 |
| Capsule endoscopy | Other | Approved | IBD | COMPLETED | NCT02182947 |
| Capsule endoscopy | Other | Approved | IBD | COMPLETED | NCT02182947 |
| Direct transfer to an Endovascular Center | Other | Approved | Stroke | COMPLETED | NCT02795962 |
| Quirem Medical Holmium-166 radioembolization microspheres | Other | Approved | HCC | COMPLETED | NCT03437382 |
| Sham Procedure | Procedure | Approved | Osteo Arthritis Knee | COMPLETED | NCT03362957 |
| Geniculate Artery Embolization | Other | Approved | Osteo Arthritis Knee | COMPLETED | NCT03362957 |
| IN.PACT Admiral™ Drug Eluting Balloon | Drug | Approved | Peripheral Arterial Disease | COMPLETED | NCT01609296 |
| IN.PACT Admiral™ Drug Eluting Balloon | Drug | Approved | Peripheral Arterial Disease | COMPLETED | NCT01609296 |
| Experimental prospective single arm evaluating the Medtronic Duo Extended Set | Other | Approved | Diabetes Mellitus, Type 1 | UNKNOWN | NCT04823312 |
| Axys EX device | Device | Approved | Peripheral Arterial Disease | WITHDRAWN | NCT04282161 |
| Stereotactic Radioablation | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT04833712 |
| Medtronic Minimed 670G 4.0 AHCL with Guardian Sensor (3) continuous glucose monitoring sensor. | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT03040414 |
| MedtronicMinimed 670G 3.0 hybrid closed loop system | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT03040414 |
| PC+S group | Other | Preclinical | Parkinson's Disease | COMPLETED | NCT02915848 |
| TMVR Implant | Other | Approved | Mitral Valve Insufficiency | TERMINATED | NCT02428010 |
| TMVR Implant | Other | Approved | Mitral Valve Insufficiency | TERMINATED | NCT02428010 |
| TMVR Implant | Other | Approved | Mitral Valve Insufficiency | TERMINATED | NCT02428010 |
| Control Group (Historical) | Other | Preclinical | Bradycardia | COMPLETED | NCT03518658 |
| Evaluation Group | Other | Preclinical | Bradycardia | COMPLETED | NCT03518658 |
| Control Group (Historical) | Other | Preclinical | Bradycardia | COMPLETED | NCT03518658 |
| Evaluation Group | Other | Preclinical | Bradycardia | COMPLETED | NCT03518658 |
| Optimal Medical Therapy | Drug | Phase PHASE2 | Dilated Cardiomyopathy | SUSPENDED | NCT03071653 |
| Left Cardiac Sympathetic Denervation (LCSD) | Other | Phase PHASE2 | Dilated Cardiomyopathy | SUSPENDED | NCT03071653 |
| Electromagnetic Navigation Bronchoscopy | Other | Preclinical | Lung Lesion(s) Requiring Evaluation | COMPLETED | NCT02410837 |
| Electromagnetic Navigation Bronchoscopy | Other | Preclinical | Lung Lesion(s) Requiring Evaluation | COMPLETED | NCT02410837 |
| PROTÉGÉ® GPS™ and PROTÉGÉ® RX Carotid Stent Systems and Spider Embolic Protection Device | Device | Phase PHASE3 | Carotid Artery Disease | COMPLETED | NCT00619775 |
| PROTÉGÉ® GPS™ and PROTÉGÉ® RX Carotid Stent Systems and Spider Embolic Protection Device | Device | Phase PHASE3 | Carotid Artery Disease | COMPLETED | NCT00619775 |
| PROTÉGÉ® GPS™ and PROTÉGÉ® RX Carotid Stent Systems and Spider Embolic Protection Device | Device | Phase PHASE3 | Carotid Artery Disease | COMPLETED | NCT00619775 |
| Clinical Reminder | Other | Phase PHASE3 | Cardiomyopathies | COMPLETED | NCT01217827 |
| Colonoscopy | Other | Approved | Inflammatory Bowel Diseases | UNKNOWN | NCT04904224 |
| Panintestinal video capsule endoscopy | Other | Approved | Inflammatory Bowel Diseases | UNKNOWN | NCT04904224 |
| HET Application | Other | Approved | Hemorrhoids | COMPLETED | NCT02773420 |
| Guardian™ Sensor (3) connected to a Guardian™ Connect Transmitter | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT03966911 |
| Scoliosis surgery | Procedure | Approved | Neuromuscular Diseases | COMPLETED | NCT03863496 |
| HeartWare Ventricular Assist Device | Device | Preclinical | End-stage Heart Failure | COMPLETED | NCT04543747 |
| HeartWare Ventricular Assist Device | Device | Preclinical | End-stage Heart Failure | COMPLETED | NCT04543747 |
| PAP (CPAP or ASV) | Other | Approved | Sleep Disordered Breathing | COMPLETED | NCT02727192 |
| Gastrisail | Other | Approved | Morbid Obesity | COMPLETED | NCT02749201 |
| Medtronic Reveal LINQ implantable cardiac monitor | Other | Approved | Myocardial Infarction | COMPLETED | NCT02594488 |
| Medtronic Reveal LINQ implantable cardiac monitor | Other | Approved | Myocardial Infarction | COMPLETED | NCT02594488 |
| Routine care | Other | Phase PHASE3 | Stroke | COMPLETED | NCT00789542 |
| Intermittent Pneumatic compression | Other | Phase PHASE3 | Stroke | COMPLETED | NCT00789542 |
| Reveal LINQ™ | Other | Approved | Fall Patients | UNKNOWN | NCT04881136 |
| Reveal LINQ™ | Other | Approved | Fall Patients | UNKNOWN | NCT04881136 |
| Fitbit | Other | Approved | ICD Patients | COMPLETED | NCT03084458 |
| Implantable System for Remodulin (treprostinil) | Other | Preclinical | Pulmonary Arterial Hypertension | WITHDRAWN | NCT03833323 |
| Implantable System for Remodulin (treprostinil) | Other | Preclinical | Pulmonary Arterial Hypertension | WITHDRAWN | NCT03833323 |
| Implantable System for Remodulin (treprostinil) | Other | Preclinical | Pulmonary Arterial Hypertension | WITHDRAWN | NCT03833323 |
| Sacral Nerve Modulation | Other | Preclinical | Urinary Incontinence | COMPLETED | NCT02186041 |
| Sacral Nerve Modulation | Other | Preclinical | Urinary Incontinence | COMPLETED | NCT02186041 |
| MR-tractography guided implantation of ACTIVA INS DBS system | Other | Approved | Essential Tremor | UNKNOWN | NCT02491554 |
| Conventional AC-PC based implantation of ACTIVA INS DBS system | Other | Approved | Essential Tremor | UNKNOWN | NCT02491554 |
| MR-tractography guided implantation of ACTIVA INS DBS system | Other | Approved | Essential Tremor | UNKNOWN | NCT02491554 |
| Conventional AC-PC based implantation of ACTIVA INS DBS system | Other | Approved | Essential Tremor | UNKNOWN | NCT02491554 |
| Medtronic HeartWare ™ HVAD™ System | Other | Preclinical | Chronic Heart Failure | WITHDRAWN | NCT04854200 |
| Medtronic HeartWare ™ HVAD™ System | Other | Preclinical | Chronic Heart Failure | WITHDRAWN | NCT04854200 |
| Novolog | Other | Phase PHASE4 | Diabetes Mellitus, Type 1 | COMPLETED | NCT03554486 |
| Fiasp | Other | Phase PHASE4 | Diabetes Mellitus, Type 1 | COMPLETED | NCT03554486 |
| Questionnaires | Other | Preclinical | Refractory Epilepsy | COMPLETED | NCT03404128 |
| CD HORIZON® Fenestrated Screw System with Fenestrated Screw Cement | Other | Approved | Degenerative Spinal Disease | TERMINATED | NCT03797144 |
| CD HORIZON® Fenestrated Screw System with Fenestrated Screw Cement | Other | Approved | Degenerative Spinal Disease | TERMINATED | NCT03797144 |
| Endovascular repair of ruptured abdominal aortic aneurysm (EVAR) with Medtronic Endurant | Other | Preclinical | Rupture, Aortic | UNKNOWN | NCT04471181 |
| Standard Infusion Set | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT04284033 |
| Extended Wear Infusion Set | Other | Approved | Type 1 Diabetes | WITHDRAWN | NCT04284033 |
| CT scan | Other | Approved | Faecal Incontinence | COMPLETED | NCT05049486 |
| ECG Vest Optimization | Other | Approved | Heart Failure | COMPLETED | NCT02699944 |
| Optimization of CRT Device | Device | Approved | Heart Failure, Systolic | COMPLETED | NCT03305692 |
| OsteoCool™ RF Ablation | Other | Approved | Metastasis Spine | COMPLETED | NCT03249584 |
| OsteoCool™ RF Ablation | Other | Approved | Metastasis Spine | COMPLETED | NCT03249584 |
| Aspirin | Other | Phase PHASE3 | Embolic Stroke of Undetermined Source | COMPLETED | NCT02427126 |
| Apixaban | Other | Phase PHASE3 | Embolic Stroke of Undetermined Source | COMPLETED | NCT02427126 |
| Cardiopulmonary exercise test with gradually increased pump speed depending on live echocardiographic imaging. | Other | Approved | Left Ventricular Assist Device | COMPLETED | NCT05063006 |
| Cardiopulmonary exercise tests with maintained baseline optimal pump speed settings. | Other | Approved | Left Ventricular Assist Device | COMPLETED | NCT05063006 |
| Cardiopulmonary exercise test with gradually increased pump speed depending on live echocardiographic imaging. | Other | Approved | Left Ventricular Assist Device | COMPLETED | NCT05063006 |
| Cardiopulmonary exercise tests with maintained baseline optimal pump speed settings. | Other | Approved | Left Ventricular Assist Device | COMPLETED | NCT05063006 |
| Control Group | Other | Approved | NF1 | TERMINATED | NCT02718131 |
| INFUSE Bone Graft (BMP-2) | Other | Approved | NF1 | TERMINATED | NCT02718131 |
| Endurant Stent Graft System | Other | Approved | Aortic Aneurysm, Abdominal | COMPLETED | NCT01379222 |
| Endurant Stent Graft System | Other | Approved | Aortic Aneurysm, Abdominal | COMPLETED | NCT01379222 |
| Talent Converter Stent Graft and Talent Occluder with Occluder Delivery System | Other | Preclinical | Abdominal Aortic Aneurysms | TERMINATED | NCT01129609 |
| Talent Converter Stent Graft and Talent Occluder with Occluder Delivery System | Other | Preclinical | Abdominal Aortic Aneurysms | TERMINATED | NCT01129609 |
| Valiant Thoracic Stent Graft with the Captivia Delivery System | Other | Approved | Aortic Dissection | COMPLETED | NCT01114724 |
| Valiant Thoracic Stent Graft with the Captivia Delivery System | Other | Approved | Blunt Thoracic Aortic Injury | COMPLETED | NCT01092767 |
| Talent Abdominal Stent Graft | Other | Approved | Aortic Aneurysm, Abdominal | COMPLETED | NCT00816062 |
| Device: Medtronic Resolute Onyx Zotarolimus-Eluting Coronary Stent System Treatment Followed by one-month DAPT | Drug | Approved | Coronary Artery Disease | COMPLETED | NCT03647475 |
| Device: Medtronic Resolute Onyx Zotarolimus-Eluting Coronary Stent System Treatment Followed by one-month DAPT | Drug | Approved | Coronary Artery Disease | COMPLETED | NCT03647475 |
| Endurant Stent graft | Other | Preclinical | Aneurysm | COMPLETED | NCT01526811 |
| Endurant Stent graft | Other | Preclinical | Aneurysm | COMPLETED | NCT01526811 |
| Fortevo Endograft | Other | Preclinical | Aortic Aneurysm, Abdominal | TERMINATED | NCT01276249 |
| Fortevo Endograft | Other | Preclinical | Aortic Aneurysm, Abdominal | TERMINATED | NCT01276249 |
| Talent Thoracic Stent Graft | Other | Phase PHASE2 | Thoracic Aortic Aneurysms | COMPLETED | NCT00604799 |
| Talent Thoracic Stent Graft | Other | Phase PHASE2 | Thoracic Aortic Aneurysms | COMPLETED | NCT00604799 |
| TALENT Aortic Cuff Abdominal Stent Graft | Other | Preclinical | Abdominal Aortic Aneurysms | NO_LONGER_AVAILABLE | NCT00604643 |
| TALENT Aortic Cuff Abdominal Stent Graft | Other | Preclinical | Abdominal Aortic Aneurysms | NO_LONGER_AVAILABLE | NCT00604643 |
| TALENT Aortic Cuff Abdominal Stent Graft | Other | Preclinical | Abdominal Aortic Aneurysms | NO_LONGER_AVAILABLE | NCT00604643 |
| Endurant Stent Graft System | Other | Approved | Abdominal Aortic Aneurysms | COMPLETED | NCT00705718 |
| Endurant Stent Graft System | Other | Approved | Abdominal Aortic Aneurysms | COMPLETED | NCT00705718 |
| Aptus Endovascular AAA Repair System | Other | Approved | Abdominal Aortic Aneurysms (AAA) | COMPLETED | NCT00507559 |
| Aptus Endovascular AAA Repair System | Other | Approved | Abdominal Aortic Aneurysms (AAA) | COMPLETED | NCT00507559 |
| Valiant Thoracic Stent Graft System | Other | Approved | Thoracic Aortic Aneurysm | COMPLETED | NCT00413231 |
| Valiant Thoracic Stent Graft System | Other | Approved | Thoracic Aortic Aneurysm | COMPLETED | NCT00413231 |
| Ellipsys Vascular Access Catheter | Other | Approved | End Stage Renal Disease | COMPLETED | NCT02363972 |
| Ellipsys Vascular Access Catheter | Other | Approved | End Stage Renal Disease | COMPLETED | NCT02363972 |
| Proteomics Analysis | Other | Phase PHASE1 | Aortic Stenosis | RECRUITING | NCT04552275 |
| InterStim Basic Evaluation lead and foramen needle | Other | Approved | Overactive Bladder | COMPLETED | NCT04016324 |
| InterStim Basic Evaluation lead and foramen needle | Other | Approved | Overactive Bladder | COMPLETED | NCT04016324 |
| InterStim Basic Evaluation lead and foramen needle | Other | Approved | Overactive Bladder | COMPLETED | NCT04016324 |
| Valiant Thoracoabdominal Stent Graft System | Other | Approved | Thoracoabdominal Aortic Aneurysm | ACTIVE_NOT_RECRUITING | NCT04009512 |
| Pipeline™ Flex Embolization Device with Shield Technology™ | Device | Preclinical | Intracranial Aneurysm | COMPLETED | NCT02719522 |
| Pipeline™ Flex Embolization Device with Shield Technology™ | Device | Preclinical | Intracranial Aneurysm | COMPLETED | NCT02719522 |
| Pipeline™ Flex Embolization Device with Shield Technology™ | Device | Preclinical | Intracranial Aneurysm | COMPLETED | NCT02719522 |
| ACTIVA® PC neurostimulator (Model 37601) | Other | Approved | Huntington Disease | COMPLETED | NCT02535884 |
| Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02660827 |
| Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02660827 |
| Parkinson's Kinetigraph | Other | Preclinical | Parkinson's Disease | COMPLETED | NCT02509325 |
| Parkinson's Kinetigraph | Other | Preclinical | Parkinson's Disease | COMPLETED | NCT02509325 |
| Sacral Neuromodulation | Other | Preclinical | Constipation | COMPLETED | NCT02961465 |
| DTA patients (Valiant) | Other | Preclinical | Aortic Aneurysm, Thoracic | COMPLETED | NCT01775046 |
| DTA patients (Valiant) | Other | Preclinical | Aortic Aneurysm, Thoracic | COMPLETED | NCT01775046 |
| Medtronic Minimed 670G 4.0 AHCL | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT04269668 |
| Medtronic Minimed 670G 3.0 HCL | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT04269668 |
| Baclofen bolus injection | Other | Phase PHASE4 | Muscle Spasticity | COMPLETED | NCT02903823 |
| iPro2 | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT05150041 |
| Guardian connect | Other | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT05150041 |
| Bi-plane fluoroscopy | Other | Preclinical | Heart Diseases | COMPLETED | NCT03941275 |
| Bi-plane fluoroscopy | Other | Preclinical | Heart Diseases | COMPLETED | NCT03941275 |
| Bi-plane fluoroscopy | Other | Preclinical | Heart Diseases | COMPLETED | NCT03941275 |
| NIRS | Other | Preclinical | HIE - Perinatal Hypoxic - Ischemic Encephalopathy | TERMINATED | NCT03835039 |
| Colonoscopy | Other | Approved | Colorectal Neoplasms | COMPLETED | NCT04673136 |
| GI-GENIUS Medtronic | Other | Approved | Colorectal Neoplasms | COMPLETED | NCT04673136 |
| Spinal cord stimulation | Other | Preclinical | Failed Back Surgery Syndrome | UNKNOWN | NCT05349695 |
| Neuro-vascular access | Other | Preclinical | Acute Ischemic Stroke | COMPLETED | NCT04416659 |
| Neuro-vascular access | Other | Preclinical | Acute Ischemic Stroke | COMPLETED | NCT04416659 |
| Neuro-vascular access | Other | Preclinical | Acute Ischemic Stroke | COMPLETED | NCT04416659 |
| dMRI Scan | Other | Preclinical | Epilepsy | COMPLETED | NCT03775694 |
| dMRI Scan | Other | Preclinical | Epilepsy | COMPLETED | NCT03775694 |
| dMRI Scan | Other | Preclinical | Epilepsy | COMPLETED | NCT03775694 |
| Visualase Thermal Therapy System | Drug | Preclinical | Epilepsy | COMPLETED | NCT03489187 |
| Visualase Thermal Therapy System | Drug | Preclinical | Epilepsy | COMPLETED | NCT03489187 |
| Saline | Other | Phase PHASE3 | Sick Sinus Syndrome | COMPLETED | NCT02809131 |
| cephalexin, or levofloxacin, or clindamycin | Other | Phase PHASE3 | Sick Sinus Syndrome | COMPLETED | NCT02809131 |
| polymixin/bacitracin | Other | Phase PHASE3 | Sick Sinus Syndrome | COMPLETED | NCT02809131 |
| Advanced hybrid closed loop system | Other | Approved | Type 1 Diabetes | COMPLETED | NCT04901143 |
| Advanced hybrid closed loop system | Other | Approved | type1diabetes | COMPLETED | NCT04479826 |
| DUO Extended Set | Other | Approved | Type 1 Diabetes | COMPLETED | NCT04810780 |
| Cardiac Resynchronization Therapy | Drug | Preclinical | Heart Failure | COMPLETED | NCT03723265 |
| Personalized Conservative Treatment | Drug | Approved | Constipation | COMPLETED | NCT02961582 |
| Sacral Neuromodulation | Other | Approved | Constipation | COMPLETED | NCT02961582 |
| PVAC GOLD catheter ablation | Other | Phase PHASE4 | Atrial Fibrillation Paroxysmal | COMPLETED | NCT04023461 |
| Medtronic Implantable Tibial Neuromodulation (TNM) System | Other | Approved | Overactive Bladder | COMPLETED | NCT04873271 |
| Medtronic Implantable Tibial Neuromodulation (TNM) System | Other | Approved | Overactive Bladder | COMPLETED | NCT04873271 |
| Reveal LINQ | Other | Preclinical | Arrhythmias, Cardiac | COMPLETED | NCT02746471 |
| Reveal LINQ | Other | Preclinical | Arrhythmias, Cardiac | COMPLETED | NCT02746471 |
| BIS | Other | Approved | Anesthesia | COMPLETED | NCT04466384 |
| BIS | Other | Approved | Anesthesia | COMPLETED | NCT04466384 |
| Deep brain stimulation | Other | Approved | Huntington Disease | UNKNOWN | NCT04244513 |
| ECG Belt | Other | Approved | Bradycardia | COMPLETED | NCT04583709 |
| MiniMed™ 670G system | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT04663295 |
| MiniMed™ 670G system | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT04663295 |
| Intravascular Ultrasound (IVUS) | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02098876 |
| Optical Coherence Tomography (OCT) | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02098876 |
| Xience Xpedition everolimus eluting stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02098876 |
| Resolute Integrity Zotarolimus eluting stent | Other | Approved | Coronary Artery Disease | COMPLETED | NCT02098876 |
| Defibrillation using the Extravascular ICD | Other | Approved | Tachycardia | WITHDRAWN | NCT05049720 |
| CAPERE Thrombectomy System | Other | Preclinical | Observational Study | TERMINATED | NCT03869645 |
| CAPERE Thrombectomy System | Other | Preclinical | Observational Study | TERMINATED | NCT03869645 |
| Medtronic Extended Mio 30 Infusion Set | Other | Approved | Diabetes Mellitus, Type 1 | COMPLETED | NCT05544643 |
| Ablation of ventricular arrhythmias + renal denervation | Other | Approved | Ventricular Tachycardia | TERMINATED | NCT02071511 |
| Ablation of ventricular arrhythmias | Other | Approved | Ventricular Tachycardia | TERMINATED | NCT02071511 |
| Bi-ventricular pacing | Other | Approved | Atrioventricular Block, Second and Third Degree | UNKNOWN | NCT05553626 |
| Left bundle branch pacing | Other | Approved | Atrioventricular Block, Second and Third Degree | UNKNOWN | NCT05553626 |
| Bi-ventricular pacing | Other | Approved | Atrioventricular Block, Second and Third Degree | UNKNOWN | NCT05553626 |
| Left bundle branch pacing | Other | Approved | Atrioventricular Block, Second and Third Degree | UNKNOWN | NCT05553626 |
| Placebo oral capsule | Other | Phase PHASE2 | Current or Recent History of Atrial Fibrillation | COMPLETED | NCT01970501 |
| metoprolol succinate | Other | Phase PHASE2 | Current or Recent History of Atrial Fibrillation | COMPLETED | NCT01970501 |
| bucindolol hydrochloride | Other | Phase PHASE2 | Current or Recent History of Atrial Fibrillation | COMPLETED | NCT01970501 |
| Laser technology for intracerebral thermocoagulation | Other | Phase PHASE1 | Drug-resistant Focal Epilepsy | UNKNOWN | NCT05198882 |
| Anti-Arrhythmic Drug Therapy | Drug | Approved | Atrial Fibrillation | UNKNOWN | NCT05514860 |
| Cryoballoon-based PVI | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT05514860 |
| Anti-Arrhythmic Drug Therapy | Drug | Approved | Atrial Fibrillation | UNKNOWN | NCT02825979 |
| Cryoballoon-based PVI | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT02825979 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01531374 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01531374 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01240902 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01240902 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01240902 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01240902 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01240902 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | COMPLETED | NCT01240902 |
| CoreValve Evolut R TAVR system | Other | Approved | Aortic Stenosis | COMPLETED | NCT02207569 |
| CoreValve Evolut R TAVR system | Other | Approved | Aortic Stenosis | COMPLETED | NCT02207569 |
| Thoracoabdominal Aortic Aneurysm Repair | Other | Approved | Thoracoabdominal Aortic Aneurysm | TERMINATED | NCT03113383 |
| Bronchoscopic ablation catheter | Other | Preclinical | Cancer, Lung | COMPLETED | NCT03569111 |
| Bronchoscopic ablation catheter | Other | Preclinical | Cancer, Lung | COMPLETED | NCT03569111 |
| Non-Invasive Controlled Hypoxia | Other | Preclinical | Hypoxia | COMPLETED | NCT05532670 |
| Non-Invasive Controlled Hypoxia | Other | Preclinical | Hypoxia | COMPLETED | NCT05532670 |
| PillCam® COLON 2 Capsule Endoscopy | Other | Approved | Crohn's Disease | COMPLETED | NCT02624414 |
| Continuous glucose monitoring system | Other | Preclinical | Diabetes Mellitus (Diagnosis) | COMPLETED | NCT04776811 |
| Continuous glucose monitoring system | Other | Preclinical | Diabetes Mellitus (Diagnosis) | COMPLETED | NCT04776811 |
| Endovascular aneurysm repair (EVAR) | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02393716 |
| Endurant Evo AAA Stent Graft System | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02393716 |
| Endovascular aneurysm repair (EVAR) | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02393716 |
| Endurant Evo AAA Stent Graft System | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02393716 |
| Electrophysiology Study | Other | Approved | Aortic Stenosis | COMPLETED | NCT04489095 |
| Surgical resection | Other | Approved | ColoRectal Cancer | UNKNOWN | NCT03088150 |
| Thermal ablation | Other | Approved | ColoRectal Cancer | UNKNOWN | NCT03088150 |
| Surgical resection | Other | Approved | ColoRectal Cancer | UNKNOWN | NCT03088150 |
| Thermal ablation | Other | Approved | ColoRectal Cancer | UNKNOWN | NCT03088150 |
| Adherence short message texts | Other | Approved | Hypertension | COMPLETED | NCT04124263 |
| Educational short message texts | Other | Approved | Hypertension | COMPLETED | NCT04124263 |
| Investigational LINQ™ HF RAMware | Other | Approved | Heart Failure | COMPLETED | NCT03608826 |
| Investigational LINQ™ HF RAMware | Other | Approved | Heart Failure | COMPLETED | NCT03608826 |
| Mendec Spine Bone Cement | Other | Approved | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | COMPLETED | NCT03730207 |
| Xpede™ Bone Cement | Other | Approved | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | COMPLETED | NCT03730207 |
| Mendec Spine Bone Cement | Other | Approved | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | COMPLETED | NCT03730207 |
| Xpede™ Bone Cement | Other | Approved | Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder) | COMPLETED | NCT03730207 |
| ECG Belt Research System | Other | Approved | Heart Failure | COMPLETED | NCT03504020 |
| ECG Belt Research System | Other | Approved | Heart Failure | COMPLETED | NCT03504020 |
| ECG Belt Research System | Other | Approved | Heart Failure | COMPLETED | NCT03504020 |
| Permacol biologic mesh | Other | Phase PHASE2 | Ventral Hernia | UNKNOWN | NCT02703662 |
| Strattice biologic mesh | Other | Phase PHASE2 | Ventral Hernia | UNKNOWN | NCT02703662 |
| Reveal LINQ ICM System | Other | Approved | Focal Epilepsy | TERMINATED | NCT03955432 |
| Preservative-free morphine sulfate (PFMS) | Other | Phase PHASE4 | Chronic Non-malignant Pain | COMPLETED | NCT03761277 |
| Medtronic SynchroMed™ II infusion system | Other | Phase PHASE4 | Chronic Non-malignant Pain | COMPLETED | NCT03761277 |
| Preservative-free morphine sulfate (PFMS) | Other | Phase PHASE4 | Chronic Non-malignant Pain | COMPLETED | NCT03761277 |
| Medtronic SynchroMed™ II infusion system | Other | Phase PHASE4 | Chronic Non-malignant Pain | COMPLETED | NCT03761277 |
| Preservative-free morphine sulfate (PFMS) | Other | Phase PHASE4 | Chronic Non-malignant Pain | COMPLETED | NCT03761277 |
| Medtronic SynchroMed™ II infusion system | Other | Phase PHASE4 | Chronic Non-malignant Pain | COMPLETED | NCT03761277 |
| PITA | Other | Approved | Heart Failure | COMPLETED | NCT04159454 |
| IPG infections | Other | Preclinical | Neuropathic Pain | UNKNOWN | NCT05735574 |
| Accelerometer Sensing for Micra AV Study | Other | Approved | AV Block | COMPLETED | NCT04245345 |
| Spinal Cord Stimulation System | Other | Approved | Chronic Pain | COMPLETED | NCT04601454 |
| Spinal Cord Stimulation System | Other | Approved | Chronic Pain | COMPLETED | NCT04601454 |
| Spinal Cord Stimulation System | Other | Approved | Chronic Pain | COMPLETED | NCT04601454 |
| Thoracolumbar Fracture Fixation | Other | Preclinical | Lumbar Vertebral Fracture | COMPLETED | NCT04495400 |
| TRIAGE HF Pathway | Other | Preclinical | Heart Failure | UNKNOWN | NCT04177199 |
| Medtronic Transcatheter Aortic Valve 2.0 Replacement System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT02738853 |
| Medtronic Transcatheter Aortic Valve 2.0 Replacement System | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT02738853 |
| Robotic-guided spine surgery | Procedure | Preclinical | Spinal Disease | UNKNOWN | NCT05181098 |
| Pacemaker system will be implanted but set to Pacing Off. | Other | Approved | Heart Failure With a Preserved Ejection Fraction | COMPLETED | NCT02145351 |
| Rate adaptive atrial pacing using a dual-chamber pacemaker | Other | Approved | Heart Failure With a Preserved Ejection Fraction | COMPLETED | NCT02145351 |
| Cyanoacrylate closure | Other | Approved | Venous Leg Ulcer | COMPLETED | NCT04011371 |
| Cyanoacrylate closure | Other | Approved | Venous Leg Ulcer | COMPLETED | NCT04011371 |
| Non-Invasive Programmed Stimulation (NIPS) | Other | Approved | Ventricular Tachycardia | TERMINATED | NCT03531502 |
| Standard Medical Therapy | Drug | Approved | Ventricular Tachycardia | TERMINATED | NCT03531502 |
| Ventricular Tachycardia Ablation | Other | Approved | Ventricular Tachycardia | TERMINATED | NCT03531502 |
| Intrathecal Baclofen Pump | Other | Preclinical | Cerebral Palsy | NOT_YET_RECRUITING | NCT05817409 |
| BIS Complete Monitoring System | Other | Approved | Anesthesia | COMPLETED | NCT04810481 |
| BIS Complete Monitoring System | Other | Approved | Anesthesia | COMPLETED | NCT04810481 |
| BIS Complete Monitoring System | Other | Approved | Anesthesia | COMPLETED | NCT04602546 |
| BIS Complete Monitoring System | Other | Approved | Anesthesia | COMPLETED | NCT04602546 |
| BIS Complete Monitoring System | Other | Approved | Anesthesia | COMPLETED | NCT04602546 |
| Activa PC+S | Other | Approved | Parkinson's Disease | COMPLETED | NCT01934296 |
| Refills (SynchroMed® II Programmable Drug Infusion Pump) | Drug | Preclinical | Severe Spasticity | COMPLETED | NCT00773019 |
| Refills (SynchroMed® II Programmable Drug Infusion Pump) | Drug | Preclinical | Severe Spasticity | COMPLETED | NCT00773019 |
| CoreValve Evolut 34R TAVR system | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT02746809 |
| CoreValve Evolut 34R TAVR system | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT02746809 |
| Valsartan | Other | Phase PHASE4 | Congestive Heart Failure | WITHDRAWN | NCT03279861 |
| Entresto | Other | Phase PHASE4 | Congestive Heart Failure | WITHDRAWN | NCT03279861 |
| CADe enabled programme (GI Genius) | Other | Preclinical | Colonic Polyp | UNKNOWN | NCT05822895 |
| Cloud-based Digital Twin and Meal Prediction algorithms | Other | Approved | Type 1 Diabetes | COMPLETED | NCT04203823 |
| Cloud-based Digital Twin and Meal Prediction algorithms | Other | Approved | Type 1 Diabetes | COMPLETED | NCT04203823 |
| Autograft/CD HORIZON® Spinal System | Other | Phase PHASE3 | Degenerative Disc Disease | COMPLETED | NCT00707265 |
| rhBMP-2/CRM/CD HORIZON® Spinal System | Other | Phase PHASE3 | Degenerative Disc Disease | COMPLETED | NCT00707265 |
| Autograft/CD HORIZON® Spinal System | Other | Phase PHASE3 | Degenerative Disc Disease | COMPLETED | NCT00707265 |
| rhBMP-2/CRM/CD HORIZON® Spinal System | Other | Phase PHASE3 | Degenerative Disc Disease | COMPLETED | NCT00707265 |
| PRESTIGE® Cervical Disc | Other | Approved | Degenerative Cervical Disc Disease | COMPLETED | NCT00642876 |
| Allograft Fusion and ATLANTIS™ Cervical Plate System | Other | Approved | Degenerative Cervical Disc Disease | COMPLETED | NCT00642876 |
| PRESTIGE® Cervical Disc | Other | Approved | Degenerative Cervical Disc Disease | COMPLETED | NCT00642876 |
| Allograft Fusion and ATLANTIS™ Cervical Plate System | Other | Approved | Degenerative Cervical Disc Disease | COMPLETED | NCT00642876 |
| rhBMP-2/CRM/CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491568 |
| rhBMP-2/CRM/CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491568 |
| rhBMP-2/CRM/CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491568 |
| rhBMP-2/BCP device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01495234 |
| rhBMP-2/BCP device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01495234 |
| Autogenous bone/allograft bone dowel | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT01494493 |
| rhBMP-2/ACS/allograft bone dowel | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT01494493 |
| Autogenous bone/allograft bone dowel | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT01494493 |
| rhBMP-2/ACS/allograft bone dowel | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT01494493 |
| Autogenous bone/allograft bone dowel | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT01494493 |
| rhBMP-2/ACS/allograft bone dowel | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT01494493 |
| Autograft/TSRH® or autograft/CD HORIZON® Spinal System. | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494454 |
| rhBMP-2/BCP/TSRH® or rhBMP-2/BCP/CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494454 |
| Autograft/TSRH® or autograft/CD HORIZON® Spinal System. | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494454 |
| rhBMP-2/BCP/TSRH® or rhBMP-2/BCP/CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494454 |
| Autogenous bone/allograft bone dowel | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494428 |
| rhBMP-2/ACS/allograft bone dowel | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494428 |
| Autogenous bone/allograft bone dowel | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494428 |
| rhBMP-2/ACS/allograft bone dowel | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494428 |
| Autogenous bone/allograft bone dowel | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494428 |
| rhBMP-2/ACS/allograft bone dowel | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01494428 |
| Autogenous Bone / CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491542 |
| INFUSE® Bone Graft/MASTERGRAFT® Granules/CD HORIZON® | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491542 |
| Autogenous Bone / CD HORIZON® Spinal System | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491542 |
| INFUSE® Bone Graft/MASTERGRAFT® Granules/CD HORIZON® | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491542 |
| Autogenous bone/INTERFIX™ | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491451 |
| rhBMP-2/ACS/INTERFIX™ | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491451 |
| Autogenous bone/INTERFIX™ | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491451 |
| rhBMP-2/ACS/INTERFIX™ | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491451 |
| Autogenous bone/INTERFIX™ | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491451 |
| rhBMP-2/ACS/INTERFIX™ | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT01491451 |
| Autogenous Bone//LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491425 |
| rhBMP-2/ACS//LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491425 |
| Autogenous Bone//LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491425 |
| rhBMP-2/ACS//LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491425 |
| Autogenous Bone/LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491386 |
| rhBMP-2/ACS/LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491386 |
| Autogenous Bone/LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491386 |
| rhBMP-2/ACS/LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491386 |
| Autogenous Bone/LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491386 |
| rhBMP-2/ACS/LT-CAGE® Device | Device | Approved | Degenerative Disc Disease | COMPLETED | NCT01491386 |
| Right Ventricular Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | UNKNOWN | NCT05869500 |
| Left Bundle Branch Area Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | UNKNOWN | NCT05869500 |
| Delayed auto mode | Other | Approved | Diabetes Mellitus Type 1 Pre-Existing | COMPLETED | NCT04420728 |
| Early auto-mode | Other | Approved | Diabetes Mellitus Type 1 Pre-Existing | COMPLETED | NCT04420728 |
| TAVR | Other | Preclinical | Aortic Stenosis | UNKNOWN | NCT03423459 |
| TAVR | Other | Preclinical | Aortic Stenosis | UNKNOWN | NCT03423459 |
| Reveal LINQ™ Insertable Cardiac Monitor | Other | Approved | Stroke, Acute | COMPLETED | NCT02700945 |
| Reveal LINQ™ Insertable Cardiac Monitor | Other | Approved | Stroke, Acute | COMPLETED | NCT02700945 |
| Reveal LINQ™ Insertable Cardiac Monitor | Other | Approved | Stroke, Acute | COMPLETED | NCT02700945 |
| GI-Genius artificial intelligence | Other | Approved | Colorectal Neoplasms | UNKNOWN | NCT05391477 |
| Continuous Glucose Monitoring | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04436822 |
| Continuous Glucose Monitoring | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04436822 |
| ATLANTIS Anterior Cervical Plate | Other | Phase PHASE3 | Cervical Degenerative Disc Disease | COMPLETED | NCT00667459 |
| PRESTIGE® LP Cervical Disc | Other | Phase PHASE3 | Cervical Degenerative Disc Disease | COMPLETED | NCT00667459 |
| ATLANTIS Anterior Cervical Plate | Other | Phase PHASE3 | Cervical Degenerative Disc Disease | COMPLETED | NCT00667459 |
| PRESTIGE® LP Cervical Disc | Other | Phase PHASE3 | Cervical Degenerative Disc Disease | COMPLETED | NCT00667459 |
| Medical management of tricuspid regurgitation | Other | Approved | Tricuspid Valve Insufficiency | COMPLETED | NCT03775759 |
| Tricuspid valve repair or replacement | Other | Approved | Tricuspid Valve Insufficiency | COMPLETED | NCT03775759 |
| Remote Monitoring of COVID-19 | Other | Preclinical | Covid19 | TERMINATED | NCT04853108 |
| Valiant Mona LSA Stent Graft System | Other | Approved | Thoracic Aortic Aneurysms | COMPLETED | NCT01839695 |
| Valiant Mona LSA Stent Graft System | Other | Approved | Thoracic Aortic Aneurysms | COMPLETED | NCT01839695 |
| NIV plus software | Other | Approved | Respiratory Distress Syndrome, Newborn | UNKNOWN | NCT05961683 |
| Neer Infrared Spectroscopy | Other | Preclinical | Respiratory Distress Syndrome, Newborn | UNKNOWN | NCT05961670 |
| Nocturnal Pacing | Other | Approved | Heart Failure, Diastolic | COMPLETED | NCT04546555 |
| Accelerated Physiologic Pacing | Other | Approved | Heart Failure, Diastolic | COMPLETED | NCT04546555 |
| Dual chamber pacemaker | Other | Approved | Heart Failure, Diastolic | COMPLETED | NCT04546555 |
| Acetominophen | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04378114 |
| Guardian™ Sensor (3) connected to a Guardian™ Connect Transmitter. Zeus sensor algorithm applied retrospectively to raw sensor data. | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04378114 |
| Guardian™ Sensor (3) connected to a Guardian™ Connect Transmitter. C sensor algorithm applied retrospectively to raw sensor data. | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04378114 |
| Acetominophen | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04378114 |
| Guardian™ Sensor (3) connected to a Guardian™ Connect Transmitter. Zeus sensor algorithm applied retrospectively to raw sensor data. | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04378114 |
| Guardian™ Sensor (3) connected to a Guardian™ Connect Transmitter. C sensor algorithm applied retrospectively to raw sensor data. | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04378114 |
| Pillcam Crohn's Capsule Endoscopy | Other | Approved | Colonic Disease | UNKNOWN | NCT06031051 |
| Atrial fibrillation catheter ablation using the Medtronic Arctic Front Ablation System | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT02217254 |
| Pan-intestinal capsule endoscopy | Other | Approved | Iron Deficiency Anemia | COMPLETED | NCT04782986 |
| Microwave ablation | Other | Approved | Lung Neoplasms | TERMINATED | NCT02673021 |
| Microwave ablation | Other | Approved | Lung Neoplasms | TERMINATED | NCT02673021 |
| A-V Impulse compression | Other | Approved | Edema | COMPLETED | NCT01389089 |
| Multi-layer compression bandage | Other | Approved | Edema | COMPLETED | NCT01389089 |
| ice gel pack | Other | Approved | Edema | COMPLETED | NCT01389089 |
| Medtronic Extended Infusion Set | Other | Approved | Diabetes | COMPLETED | NCT06074965 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System(34/38 mm) | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT03118531 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System(34/38 mm) | Other | Approved | Ischemic Heart Disease | COMPLETED | NCT03118531 |
| ICD implantation | Other | Preclinical | Valvular Heart Disease | TERMINATED | NCT03590730 |
| pacemaker follow-up | Other | Preclinical | Bradycardia | COMPLETED | NCT06094114 |
| pacemaker follow-up | Other | Preclinical | Bradycardia | COMPLETED | NCT06094114 |
| TRUFILL | Other | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| Onyx | Other | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| TRUFILL | Other | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| Onyx | Other | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| TRUFILL | Other | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| Onyx | Other | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| D-dimer assay before ablation of atrial fibrillation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02199080 |
| Capnography | Other | Preclinical | Chronic Obstructive Pulmonary Disease | UNKNOWN | NCT06108973 |
| Capnography | Other | Preclinical | Chronic Obstructive Pulmonary Disease | UNKNOWN | NCT06108973 |
| Conventional pacemaker type Medtronic Advisa ADSR03 or Azure XT VR | Other | Approved | Pacing-Induced Cardiomyopathy | COMPLETED | NCT06100757 |
| Micra Transcatheter Pacing System (TPS° | Other | Approved | Pacing-Induced Cardiomyopathy | COMPLETED | NCT06100757 |
| mesh fixation by staples | Other | Approved | Ventral Hernia | COMPLETED | NCT00773851 |
| mesh fixation by transfacial sutures | Other | Approved | Ventral Hernia | COMPLETED | NCT00773851 |
| mesh fixation by staples | Other | Approved | Ventral Hernia | COMPLETED | NCT00773851 |
| mesh fixation by transfacial sutures | Other | Approved | Ventral Hernia | COMPLETED | NCT00773851 |
| mesh fixation by staples | Other | Approved | Ventral Hernia | COMPLETED | NCT00773851 |
| mesh fixation by transfacial sutures | Other | Approved | Ventral Hernia | COMPLETED | NCT00773851 |
| TEVAR | Other | Preclinical | Aortic Aneurysm, Thoracic | TERMINATED | NCT01181947 |
| TEVAR | Other | Preclinical | Aortic Aneurysm, Thoracic | TERMINATED | NCT01181947 |
| Cryoballoon PVI | Other | Approved | Atrial Flutter Typical | COMPLETED | NCT03401099 |
| Radiofrequency ablation of CTI | Other | Approved | Atrial Flutter Typical | COMPLETED | NCT03401099 |
| Cryoballoon PVI | Other | Approved | Atrial Flutter Typical | COMPLETED | NCT03401099 |
| Radiofrequency ablation of CTI | Other | Approved | Atrial Flutter Typical | COMPLETED | NCT03401099 |
| Catheter ablation using irrigated radiofrequency current ablation or cryothermal energy | Other | Approved | Atrial Fibrillation | UNKNOWN | NCT04056390 |
| aspirin | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT01938248 |
| Apixaban | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT01938248 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT03063749 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Preclinical | Coronary Artery Disease | COMPLETED | NCT03063749 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT03584464 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT03584464 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Coronary Artery Disease | COMPLETED | NCT03584464 |
| Radiofrequency Catheter (ThermoCool Smarttouch) | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03706677 |
| Cryoballoon (Arctic Front Advance Cryoballoon) | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03706677 |
| Radiofrequency Catheter (ThermoCool Smarttouch) | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03706677 |
| Cryoballoon (Arctic Front Advance Cryoballoon) | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03706677 |
| aCRT OFF | Other | Approved | Heart Failure With Left Bundle Branch Block | COMPLETED | NCT02205359 |
| aCRT ON | Other | Approved | Heart Failure With Left Bundle Branch Block | COMPLETED | NCT02205359 |
| aCRT OFF | Other | Approved | Heart Failure With Left Bundle Branch Block | COMPLETED | NCT02205359 |
| aCRT ON | Other | Approved | Heart Failure With Left Bundle Branch Block | COMPLETED | NCT02205359 |
| aCRT OFF | Other | Approved | Heart Failure With Left Bundle Branch Block | COMPLETED | NCT02205359 |
| aCRT ON | Other | Approved | Heart Failure With Left Bundle Branch Block | COMPLETED | NCT02205359 |
| Surgical RF Ablation | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00506493 |
| Cardioblate Surgical Ablation System | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00506493 |
| Surgical RF Ablation | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00506493 |
| Cardioblate Surgical Ablation System | Other | Phase PHASE3 | Atrial Fibrillation | COMPLETED | NCT00506493 |
| ILR implantation | Other | Preclinical | Covid19 | COMPLETED | NCT04726150 |
| HeartWare Ventricular Assist Device | Device | Preclinical | Chronic Heart Failure | COMPLETED | NCT03697980 |
| HeartWare Ventricular Assist Device | Device | Preclinical | Chronic Heart Failure | COMPLETED | NCT03697980 |
| HeartWare Ventricular Assist Device | Device | Preclinical | Chronic Heart Failure | COMPLETED | NCT03697980 |
| EndoFLIP | Other | Approved | GERD | UNKNOWN | NCT06159972 |
| prospective follow-up with videocapsule | Other | Approved | Crohn Disease | UNKNOWN | NCT03889613 |
| Radiofrequency ablation | Other | Approved | Esophageal Cancer | SUSPENDED | NCT02146508 |
| Endoscopic Mucosal Resection (EMR) | Other | Approved | Esophageal Cancer | SUSPENDED | NCT02146508 |
| Radiofrequency ablation | Other | Approved | Esophageal Cancer | SUSPENDED | NCT02146508 |
| Endoscopic Mucosal Resection (EMR) | Other | Approved | Esophageal Cancer | SUSPENDED | NCT02146508 |
| Coronary Angiography | Other | Approved | Coronary Angiography | UNKNOWN | NCT05075590 |
| Standard of Care | Other | Approved | Heart Failure | COMPLETED | NCT00643279 |
| Chronicle Implantable Hemodynamic Monitor | Other | Approved | Heart Failure | COMPLETED | NCT00643279 |
| Standard of Care | Other | Approved | Heart Failure | COMPLETED | NCT00643279 |
| Chronicle Implantable Hemodynamic Monitor | Other | Approved | Heart Failure | COMPLETED | NCT00643279 |
| Defibrillation using the Extravascular ICD | Other | Approved | Tachycardia | COMPLETED | NCT03608670 |
| Defibrillation using the Extravascular ICD | Other | Approved | Tachycardia | COMPLETED | NCT03608670 |
| Medtronic Evolut™ PRO+ System | Other | Approved | Aortic Valve Stenosis | TERMINATED | NCT04639258 |
| Medtronic Evolut™ PRO+ System | Other | Approved | Aortic Valve Stenosis | TERMINATED | NCT04639258 |
| Medtronic Evolut™ PRO+ System | Other | Approved | Aortic Valve Stenosis | TERMINATED | NCT04639258 |
| Conventional CABG | Other | Approved | Coronary Artery Disease | RECRUITING | NCT03447938 |
| MICS CABG | Other | Approved | Coronary Artery Disease | RECRUITING | NCT03447938 |
| Bowel prep combination | Other | Approved | Healthy | TERMINATED | NCT03301909 |
| PillCam™ Endoscopy System | Other | Approved | Healthy | TERMINATED | NCT03301909 |
| Bowel prep combination | Other | Approved | Healthy | TERMINATED | NCT03301909 |
| PillCam™ Endoscopy System | Other | Approved | Healthy | TERMINATED | NCT03301909 |
| Non-Referred group | Other | Preclinical | Sudden Cardiac Arrest | COMPLETED | NCT03715790 |
| EP referred group | Other | Preclinical | Sudden Cardiac Arrest | COMPLETED | NCT03715790 |
| Non-Referred group | Other | Preclinical | Sudden Cardiac Arrest | COMPLETED | NCT03715790 |
| EP referred group | Other | Preclinical | Sudden Cardiac Arrest | COMPLETED | NCT03715790 |
| MiniMed 780G system | Other | Approved | Diabetes Type 1 | UNKNOWN | NCT06207838 |
| empirical stimulation | Other | Approved | Parkinson's Disease | UNKNOWN | NCT06239454 |
| interleaving stimulation | Other | Approved | Parkinson's Disease | UNKNOWN | NCT06239454 |
| AAI-DDD 50 pacing program | Other | Approved | Symptomatic First-degree Heart Block | UNKNOWN | NCT06245304 |
| DDD-50 pacing program | Other | Approved | Symptomatic First-degree Heart Block | UNKNOWN | NCT06245304 |
| Dual chamber Medtronic pacemaker implantation. | Other | Approved | Symptomatic First-degree Heart Block | UNKNOWN | NCT06245304 |
| Medtronic Valiant Thoracoabdominal Stent Graft System | Other | Approved | Thoracoabdominal Aneurysm | RECRUITING | NCT03111459 |
| Colectomy | Other | Preclinical | Colonic Neoplasms | COMPLETED | NCT04310839 |
| Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT05672823 |
| Video and kinematic data recording of minimally invasive surgical procedure | Procedure | Preclinical | Prostate Cancer | UNKNOWN | NCT05279287 |
| Open-loop testing, Closed-loop testing - External Spinal Cord Stimulator (SCS) | Other | Approved | Chronic Pain | COMPLETED | NCT04765735 |
| Open-loop testing, Closed-loop testing - External Spinal Cord Stimulator (SCS) | Other | Approved | Chronic Pain | COMPLETED | NCT04765735 |
| Hybrid Surgery | Procedure | Preclinical | Incisional Hernia of Midline of Abdomen | NOT_YET_RECRUITING | NCT06286124 |
| GI Genius (GIG) | Other | Preclinical | Colonic Polyp | UNKNOWN | NCT05870332 |
| Sorin Spiderflash-t | Other | Approved | Stroke | COMPLETED | NCT02428140 |
| Medtronic Reveal LINQ | Other | Approved | Stroke | COMPLETED | NCT02428140 |
| IN.PACT™ Admiral™ Drug Coated Balloon (DCB) | Drug | Preclinical | Obstructive Disease | UNKNOWN | NCT04597307 |
| NIRS monitoring | Other | Preclinical | Circulatory Failure | COMPLETED | NCT03814564 |
| Transcatheter Pulmonary Valve replacement | Other | Approved | Congenital Heart Defects | COMPLETED | NCT00740870 |
| Transcatheter Pulmonary Valve replacement | Other | Approved | Congenital Heart Defects | COMPLETED | NCT00740870 |
| Endovascular aneurysm repair (EVAR) | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02461524 |
| Endurant Evo AAA Stent Graft System | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02461524 |
| Endovascular aneurysm repair (EVAR) | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02461524 |
| Endurant Evo AAA Stent Graft System | Other | Approved | Abdominal Aortic Aneurysm | TERMINATED | NCT02461524 |
| PRESTIGE LP™ Cervical Disc | Other | Approved | Cervical Degenerative Disc Disease | TERMINATED | NCT03062657 |
| PRESTIGE LP™ Cervical Disc | Other | Approved | Cervical Degenerative Disc Disease | TERMINATED | NCT03062657 |
| Valiant Evo Thoracic Stent Graft System | Other | Approved | Aortic Aneurysm, Thoracic | COMPLETED | NCT02652949 |
| Valiant Evo Thoracic Stent Graft System | Other | Approved | Aortic Aneurysm, Thoracic | COMPLETED | NCT02652949 |
| Valiant Evo Thoracic Stent Graft System | Other | Approved | Aortic Aneurysm, Thoracic | COMPLETED | NCT02625324 |
| Valiant Evo Thoracic Stent Graft System | Other | Approved | Aortic Aneurysm, Thoracic | COMPLETED | NCT02625324 |
| 18F-sodium fluoride Positron Emission Tomography (18F-NaF PET), Cardiac Computed Tomography (CT), Transthoracic Echocardiography (TTE) | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT05758662 |
| 17mm MDT-2215 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | COMPLETED | NCT02686814 |
| Right ventricular pacing | Other | Approved | Cardiac Pacing | RECRUITING | NCT04595487 |
| Left ventricular septal pacing | Other | Approved | Cardiac Pacing | RECRUITING | NCT04595487 |
| Implantable Loop Recorder Insertion | Other | Approved | Obstructive Sleep Apnea | COMPLETED | NCT01058551 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | COMPLETED | NCT04311086 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | COMPLETED | NCT04311086 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | COMPLETED | NCT04311086 |
| Tourniquet | Other | Approved | Knee Replacement | COMPLETED | NCT04016285 |
| Aquamantys | Other | Approved | Knee Replacement | COMPLETED | NCT04016285 |
| Responsive deep brain stimulation | Other | Approved | Essential Tremor | COMPLETED | NCT03051178 |
| Parietene DS Composite Mesh | Other | Approved | Ventral Hernia | COMPLETED | NCT03495154 |
| Parietene DS Composite Mesh | Other | Approved | Ventral Hernia | COMPLETED | NCT03495154 |
| MRI Guided Transrectal Periuretheral Transitional Zone Ablation | Other | Approved | BPH | COMPLETED | NCT03131544 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | ACTIVE_NOT_RECRUITING | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | ACTIVE_NOT_RECRUITING | NCT02748434 |
| Signia™ Stapling System | Other | Preclinical | Abdominal Injury | COMPLETED | NCT03515811 |
| Signia™ Stapling System | Other | Preclinical | Abdominal Injury | COMPLETED | NCT03515811 |
| Signia™ Stapling System | Other | Preclinical | Abdominal Injury | COMPLETED | NCT03515811 |
| Expectant management | Other | Approved | Retained Products of Conception | RECRUITING | NCT04804332 |
| Operative hysteroscopy | Other | Approved | Retained Products of Conception | RECRUITING | NCT04804332 |
| Medtronic 780G insulin pump | Other | Approved | Type 1 Diabetes | RECRUITING | NCT06414564 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Standard Balloon Angioplasty | Other | Approved | Arteriovenous Fistula Stenosis | COMPLETED | NCT03041467 |
| IN.PACT AV DCB | Other | Approved | Arteriovenous Fistula Stenosis | COMPLETED | NCT03041467 |
| Standard Balloon Angioplasty | Other | Approved | Arteriovenous Fistula Stenosis | COMPLETED | NCT03041467 |
| IN.PACT AV DCB | Other | Approved | Arteriovenous Fistula Stenosis | COMPLETED | NCT03041467 |
| Neurothrombectomy | Other | Preclinical | Acute Ischemic Stroke | COMPLETED | NCT05005962 |
| Neurothrombectomy | Other | Preclinical | Acute Ischemic Stroke | COMPLETED | NCT05005962 |
| Medtronic DBS system | Other | Preclinical | Parkinson's Disease | COMPLETED | NCT01750242 |
| Medtronic DBS system | Other | Preclinical | Parkinson's Disease | COMPLETED | NCT01750242 |
| Medtronic DBS system | Other | Preclinical | Parkinson's Disease | COMPLETED | NCT01750242 |
| Bispectral (BIS™) Complete Monitoring System | Other | Approved | Anesthesia | COMPLETED | NCT04765046 |
| Bispectral (BIS™) Complete Monitoring System | Other | Approved | Anesthesia | COMPLETED | NCT04765046 |
| Sophono Bone Conduction Hearing Systems | Other | Preclinical | Conductive Hearing Loss | COMPLETED | NCT03143257 |
| Sophono Bone Conduction Hearing Systems | Other | Preclinical | Conductive Hearing Loss | COMPLETED | NCT03143257 |
| Sophono Bone Conduction Hearing Systems | Other | Preclinical | Conductive Hearing Loss | COMPLETED | NCT03143257 |
| MiniMed™ 780G System | Other | Preclinical | Type 1 Diabetes | COMPLETED | NCT04308291 |
| MiniMed™ 780G System | Other | Preclinical | Type 1 Diabetes | COMPLETED | NCT04308291 |
| absorbable mesh fixation | Other | Approved | Ventral Hernia | COMPLETED | NCT01109771 |
| permanent mesh fixation | Other | Approved | Ventral Hernia | COMPLETED | NCT01109771 |
| absorbable mesh fixation | Other | Approved | Ventral Hernia | COMPLETED | NCT01109771 |
| permanent mesh fixation | Other | Approved | Ventral Hernia | COMPLETED | NCT01109771 |
| absorbable mesh fixation | Other | Approved | Ventral Hernia | COMPLETED | NCT01109771 |
| permanent mesh fixation | Other | Approved | Ventral Hernia | COMPLETED | NCT01109771 |
| Spinal Cord Stimulator | Other | Approved | Chronic Pain | COMPLETED | NCT06499220 |
| Spinal Cord Stimulator | Other | Approved | Chronic Pain | COMPLETED | NCT06499220 |
| Spinal Cord Stimulator | Other | Approved | Chronic Pain | COMPLETED | NCT06499220 |
| Control group | Other | Approved | Anesthesia | RECRUITING | NCT04825847 |
| BIS monitor | Other | Approved | Anesthesia | RECRUITING | NCT04825847 |
| Aspirin | Other | Phase PHASE4 | Transcatheter Aortic Valve Replacement | COMPLETED | NCT02735902 |
| Vitamin K antagonist or direct oral anticoagulant treatment | Drug | Phase PHASE4 | Transcatheter Aortic Valve Replacement | COMPLETED | NCT02735902 |
| Retrospective data collection | Other | Preclinical | Peripheral Arterial Disease | COMPLETED | NCT04496544 |
| Enabling Sensor Research Holter Mode feature | Other | Preclinical | Heart Failure | COMPLETED | NCT06089694 |
| Enabling Sensor Research Holter Mode feature | Other | Preclinical | Heart Failure | COMPLETED | NCT06089694 |
| Medtronic Intellis™ and Vanta™ | Other | Preclinical | Chronic Pain | COMPLETED | NCT04725838 |
| Mosaic model 305, model 310, and ultra model 305 | Other | Preclinical | Heart Valve Diseases | COMPLETED | NCT03139721 |
| Monopolar electrocautery | Other | Approved | Lung Cancer | COMPLETED | NCT03125798 |
| LigaSure™ | Other | Approved | Lung Cancer | COMPLETED | NCT03125798 |
| Sacral neuromodulation | Other | Preclinical | Overactive Bladder Syndrome | COMPLETED | NCT05313984 |
| Usual care | Other | Approved | Physical Activity | COMPLETED | NCT03052829 |
| Physical activity counseling | Other | Approved | Physical Activity | COMPLETED | NCT03052829 |
| Thunderbeat | Other | Approved | Postoperative Inflammation | COMPLETED | NCT03356626 |
| Ligasure Maryland | Other | Approved | Postoperative Inflammation | COMPLETED | NCT03356626 |
| ULTRACISION Harmonic Scalpel | Other | Approved | Postoperative Inflammation | COMPLETED | NCT03356626 |
| Thunderbeat | Other | Approved | Postoperative Inflammation | COMPLETED | NCT03356626 |
| Ligasure Maryland | Other | Approved | Postoperative Inflammation | COMPLETED | NCT03356626 |
| ULTRACISION Harmonic Scalpel | Other | Approved | Postoperative Inflammation | COMPLETED | NCT03356626 |
| Elevated night pacing off | Other | Approved | Heart Failure | COMPLETED | NCT03210402 |
| Elevated night pacing on | Other | Approved | Heart Failure | COMPLETED | NCT03210402 |
| Elevated night pacing off | Other | Approved | Heart Failure | COMPLETED | NCT03210402 |
| Elevated night pacing on | Other | Approved | Heart Failure | COMPLETED | NCT03210402 |
| HSCT Patients | Other | Preclinical | Hematopoietic Stem Cell Transplant | COMPLETED | NCT04118530 |
| Pacing rate of 60 bpm | Other | Approved | Atrial Fibrillation, Persistent | RECRUITING | NCT06445439 |
| Pacing rate of 80 bpm | Other | Approved | Atrial Fibrillation, Persistent | RECRUITING | NCT06445439 |
| PillCam Colon2 procedure with MB-MMX | Procedure | Approved | Colorectal Cancer | COMPLETED | NCT05022719 |
| PillCam Colon2 procedure with MB-MMX | Procedure | Approved | Colorectal Cancer | COMPLETED | NCT05022719 |
| RAS prostatectomy and RAS cholecystectomy | Other | Preclinical | Prostate Cancer | COMPLETED | NCT05715827 |
| RAS prostatectomy and RAS cholecystectomy | Other | Preclinical | Prostate Cancer | COMPLETED | NCT05715827 |
| Radiofrequency ablation alone, no further renal denervation | Other | Phase PHASE4 | Hypertension, Uncontrolled | RECRUITING | NCT06676553 |
| Radiofrequency ablation alone, re-denervation to main and/or branch renal artery | Other | Phase PHASE4 | Hypertension, Uncontrolled | RECRUITING | NCT06676553 |
| Conventional Medical Management (CMM) | Other | Approved | Pain, Intractable | COMPLETED | NCT06442410 |
| DTM™ spinal cord stimulation therapy delivered via Intellis™ neurostimulator system | Drug | Approved | Pain, Intractable | COMPLETED | NCT06442410 |
| Conventional Medical Management (CMM) | Other | Approved | Pain, Intractable | COMPLETED | NCT06442410 |
| DTM™ spinal cord stimulation therapy delivered via Intellis™ neurostimulator system | Drug | Approved | Pain, Intractable | COMPLETED | NCT06442410 |
| Intravenous thrombolysis with recombinant tissue-type plasminogen activator (IV t-PA) | Other | Approved | Ischemic Stroke | COMPLETED | NCT03192332 |
| Stent-retriever thrombectomy with revascularization device of the Solitaire™ type | Device | Approved | Ischemic Stroke | COMPLETED | NCT03192332 |
| Novapak Nasal Sinus Packing and Stent | Other | Preclinical | Nasal Airway Obstruction | COMPLETED | NCT05747014 |
| Novapak Nasal Sinus Packing and Stent | Other | Preclinical | Nasal Airway Obstruction | COMPLETED | NCT05747014 |
| ProGrip™ Self-Gripping Polyester Mesh | Other | Approved | Incisional Hernia | RECRUITING | NCT04794582 |
| Left bundle branch area pacing followed by right ventricular septal pacing | Other | Approved | Complete Heart Block | ACTIVE_NOT_RECRUITING | NCT05541679 |
| Right ventricular septal pacing followed by left bundle branch area pacing | Other | Approved | Complete Heart Block | ACTIVE_NOT_RECRUITING | NCT05541679 |
| Guardian™ Connect system, InPen™ Basal smart cap, smart insulin pens, and InPen™ Diabetes Management app | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04809285 |
| Guardian™ Connect system, InPen™ Basal smart cap, smart insulin pens, and InPen™ Diabetes Management app | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT04809285 |
| antegrade and retrograde approach | Other | Preclinical | Chronic Total Occlusion of Coronary Artery | RECRUITING | NCT03667196 |
| Spinal Cord Stimulation | Other | Approved | Limb Pain | TERMINATED | NCT03763708 |
| Spinal Cord Stimulation | Other | Approved | Limb Pain | TERMINATED | NCT03763708 |
| Spinal Cord Stimulation | Other | Approved | Limb Pain | TERMINATED | NCT03763708 |
| AHCL insulin pump system | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT03959423 |
| AHCL insulin pump system | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT03959423 |
| Visualase MRI-Guided Laser Ablation | Other | Approved | Temporal Lobe Epilepsy | COMPLETED | NCT02844465 |
| Visualase MRI-Guided Laser Ablation | Other | Approved | Temporal Lobe Epilepsy | COMPLETED | NCT02844465 |
| TAAA Debranching Stent Graft System | Other | Approved | Thoracoabdominal Aortic Aneurysms | ACTIVE_NOT_RECRUITING | NCT03075748 |
| Radiofrequency Ablation (RFA) | Other | Approved | Oncology | ACTIVE_NOT_RECRUITING | NCT04375891 |
| Radiation Therapy | Drug | Approved | Oncology | ACTIVE_NOT_RECRUITING | NCT04375891 |
| Pacemaker: AV optimised, His pacing. | Other | Approved | Heart Failure | COMPLETED | NCT02671903 |
| Measuring the ACT to determine effect of heparin | Other | Preclinical | Arterial Disease | COMPLETED | NCT03426293 |
| Pacemaker lower rate setting | Other | Preclinical | Sinus Node Dysfunction | COMPLETED | NCT05766462 |
| Pacemaker lower rate setting | Other | Preclinical | Sinus Node Dysfunction | COMPLETED | NCT05766462 |
| Profile 3D™ and CG Future® annuloplasty system | Other | Preclinical | Mitral Valve Disease | COMPLETED | NCT03283722 |
| Profile 3D™ and CG Future® annuloplasty system | Other | Preclinical | Mitral Valve Disease | COMPLETED | NCT03283722 |
| ArcticLine Cardiac Cryoablation Catheter | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03604263 |
| ArcticLine Cardiac Cryoablation Catheter | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03604263 |
| No interventions - retrospective data collection | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT03314753 |
| No interventions - retrospective data collection | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT03314753 |
| Antiarrhythmic drug | Drug | Approved | Atrial Fibrillation | COMPLETED | NCT03118518 |
| Cryoablation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03118518 |
| Antiarrhythmic drug | Drug | Approved | Atrial Fibrillation | COMPLETED | NCT03118518 |
| Cryoablation | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03118518 |
| Arctic Front Advance Cardiac CryoAblation Catheter | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03012841 |
| Arctic Front Advance Cardiac CryoAblation Catheter | Other | Approved | Atrial Fibrillation | COMPLETED | NCT03012841 |
| Radio frequency (RF) Cardiac ablation | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT02821351 |
| Radio frequency (RF) Cardiac ablation | Other | Approved | Paroxysmal Atrial Fibrillation | COMPLETED | NCT02821351 |
| Holter monitoring | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02213731 |
| Holter monitoring | Other | Approved | Atrial Fibrillation | COMPLETED | NCT02213731 |
| Medtronic Phased RF Ablation System | Other | Approved | Persistent Atrial Fibrillation | TERMINATED | NCT01693120 |
| Medtronic Phased RF Ablation System | Other | Approved | Persistent Atrial Fibrillation | TERMINATED | NCT01693120 |
| Freezor Xtra Cryoablation Catheter | Other | Phase PHASE3 | AtrioVentricular Nodal Reentrant Tachycardia | COMPLETED | NCT01426425 |
| Freezor Xtra Cryoablation Catheter | Other | Phase PHASE3 | AtrioVentricular Nodal Reentrant Tachycardia | COMPLETED | NCT01426425 |
| Freezor Xtra Cryoablation Catheter | Other | Phase PHASE3 | AtrioVentricular Nodal Reentrant Tachycardia | COMPLETED | NCT01426425 |
| Pacing Algorithms | Other | Approved | Atrial Fibrillation, Bradycardia | COMPLETED | NCT00267137 |
| Pacing Algorithms | Other | Approved | Atrial Fibrillation, Bradycardia | COMPLETED | NCT00267137 |
| QoL EQ5D questionaire | Other | Preclinical | GAVE - Gastric Antral Vascular Ectasia | NOT_YET_RECRUITING | NCT06830317 |
| Endoscopic Radiofrequency treatment | Drug | Preclinical | GAVE - Gastric Antral Vascular Ectasia | NOT_YET_RECRUITING | NCT06830317 |
| Insulin Pump with Continuous Glucose Monitoring | Other | Approved | Type 1 Diabetes | COMPLETED | NCT05714059 |
| Insulin Pump with Continuous Glucose Monitoring | Other | Approved | Type 1 Diabetes | COMPLETED | NCT05714059 |
| Epidural Electrical Stimulation (EES) using an implanted paddle lead and pulse generator combined with a 12-month intensive rehabilitation program. | Other | Approved | Spinal Cord Injuries (SCI) | RECRUITING | NCT06847295 |
| Transcatheter aortic valve implantation | Other | Approved | Aortic Valve Stenosis | RECRUITING | NCT06874465 |
| Transcatheter aortic valve implantation | Other | Approved | Aortic Valve Stenosis | RECRUITING | NCT06874465 |
| Mesentery fixation method | Other | Approved | Petersen's Hernia | ACTIVE_NOT_RECRUITING | NCT05105360 |
| Closure method of Petersen's space | Other | Approved | Petersen's Hernia | ACTIVE_NOT_RECRUITING | NCT05105360 |
| Balloon cryoablation | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT02785991 |
| INFUSE™ Bone Graft | Other | Preclinical | Intervertebral Disc Degeneration | RECRUITING | NCT05299762 |
| INFUSE™ Bone Graft | Other | Preclinical | Intervertebral Disc Degeneration | RECRUITING | NCT05299762 |
| Medtronic Infinity Occipitocervical-Upper Thoracic System using the O-arm Imaging System and StealthStation Navigation system | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT04056520 |
| Sham Procedure | Procedure | Approved | Hypertension | COMPLETED | NCT02439749 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | COMPLETED | NCT02439749 |
| Sham Procedure | Procedure | Approved | Hypertension | COMPLETED | NCT02439749 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | COMPLETED | NCT02439749 |
| No educational or implementation tool will be provided | Other | Approved | Stroke | NOT_YET_RECRUITING | NCT06606054 |
| Educational and implementation Neurocardiology tool | Other | Approved | Stroke | NOT_YET_RECRUITING | NCT06606054 |
| ACDF interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Titan nanoLOCK interbody cage | Other | Approved | Cervical Radiculopathy | ENROLLING_BY_INVITATION | NCT05762055 |
| Placebo | Other | Phase PHASE3 | Stroke, Ischemic | RECRUITING | NCT05199194 |
| Tenecteplase | Other | Phase PHASE3 | Stroke, Ischemic | RECRUITING | NCT05199194 |
| Computed tomography scan | Other | Preclinical | New-onset Atrial Fibrillation (NOAF) | RECRUITING | NCT04964765 |
| Mapping | Other | Preclinical | New-onset Atrial Fibrillation (NOAF) | RECRUITING | NCT04964765 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT05294445 |
| Ablation of atrial fibrillation (AF) | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT05294445 |
| TBI | Other | Preclinical | Peripheral Artery Disease | TERMINATED | NCT04120610 |
| ABI | Other | Preclinical | Peripheral Artery Disease | TERMINATED | NCT04120610 |
| FlowMet-R | Other | Preclinical | Peripheral Artery Disease | TERMINATED | NCT04120610 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Robotic-Assisted Surgery (RAS) Hernia Repair Surgery | Procedure | Approved | Inguinal Hernia | ACTIVE_NOT_RECRUITING | NCT06445504 |
| Pain Management Strategies | Other | Approved | Cancer Pain | COMPLETED | NCT05366413 |
| Early Referral | Other | Approved | Cancer Pain | COMPLETED | NCT05366413 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Ellipsys Vascular Access System | Other | Approved | Renal Disease, End Stage | COMPLETED | NCT04484220 |
| Terumo TR Band Radial Compression Device | Device | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Terumo Glidesheath Slender | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Volcano based pressure wires Verrata, Verrata Plus and any subsequent marketed Volcano pressure wire technology | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Medtronic Resolute family of stents | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Multi-vessel Disease, Complete Revascularization | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Multi-vessel Disease, Culprit Vessel Only | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Single Vessel Disease | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Terumo TR Band Radial Compression Device | Device | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Terumo Glidesheath Slender | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Volcano based pressure wires Verrata, Verrata Plus and any subsequent marketed Volcano pressure wire technology | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Medtronic Resolute family of stents | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Multi-vessel Disease, Complete Revascularization | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Multi-vessel Disease, Culprit Vessel Only | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Single Vessel Disease | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Terumo TR Band Radial Compression Device | Device | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Terumo Glidesheath Slender | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Volcano based pressure wires Verrata, Verrata Plus and any subsequent marketed Volcano pressure wire technology | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Medtronic Resolute family of stents | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Multi-vessel Disease, Complete Revascularization | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Multi-vessel Disease, Culprit Vessel Only | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| Single Vessel Disease | Other | Approved | Myocardial Infarction | TERMINATED | NCT02939976 |
| FEVAR treatment : Fenestrated endograft | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| ESAR treatment: Endograft + Heli-FX Endoanchor | Drug | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT04503395 |
| Non-invasive ECG imaging - CardioInsight test | Other | Approved | Hypertrophic Cardiomyopathy | ACTIVE_NOT_RECRUITING | NCT04157205 |
| LINQ/LINQ II | Other | Preclinical | Atrial Arrhythmia | COMPLETED | NCT05488470 |
| LINQ/LINQ II | Other | Preclinical | Atrial Arrhythmia | COMPLETED | NCT05488470 |
| Observational data collection from patients with chronic rhinosinusitis (CRS) receiving PROPEL sinus implant(s) following functional endoscopic sinus surgery (FESS) | Procedure | Preclinical | Chronic Rhinosinusitis (CRS) | WITHDRAWN | NCT06671561 |
| Catheter mapping and ablation with the Sphere-9 Catheter and Affera Mapping and Ablation System | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04211441 |
| Catheter mapping and ablation with the Sphere-9 Catheter and Affera Mapping and Ablation System | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04211441 |
| Catheter mapping and ablation with the Sphere-9 Catheter and Affera Mapping and Ablation System | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT04210622 |
| Catheter mapping and ablation with the Sphere-9 Catheter and Affera Mapping and Ablation System | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT04210622 |
| Catheter mapping and ablation with the Sphere-9 Catheter and Affera Mapping and Ablation System | Other | Preclinical | Atrial Fibrillation | COMPLETED | NCT04210622 |
| PAV+ ventilation strategy | Other | Approved | Critically Ill | COMPLETED | NCT02447692 |
| PSV ventilation strategy | Other | Approved | Critically Ill | COMPLETED | NCT02447692 |
| Pacemaker | Other | Approved | Pacemaker Implantation | RECRUITING | NCT06690333 |
| Continuous Glucose Monitoring | Other | Approved | Type 1 Diabetes Mellitus | WITHDRAWN | NCT06719531 |
| Continuous Glucose Monitoring | Other | Approved | Type 1 Diabetes Mellitus | WITHDRAWN | NCT06719531 |
| Medtronic ICD with Opti Vol-Monitor | Other | Approved | Ischemic and Non-ischemic Cardiomyopathy | TERMINATED | NCT04206501 |
| Coronary artery bypass surgery | Procedure | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| Minimally Invasive Coronary Artery Bypass Grafting | Other | Approved | Coronary Arterial Disease (CAD) | ENROLLING_BY_INVITATION | NCT06794359 |
| NIRS evaluation | Other | Preclinical | Congenital Heart Defect | RECRUITING | NCT04106479 |
| MiniMed 780G Auto Mode with DS5 sensor | Other | Approved | Diabetes type1 | COMPLETED | NCT05574062 |
| MiniMed 780G Manual Mode with G4S sensor | Other | Approved | Diabetes type1 | COMPLETED | NCT05574062 |
| MiniMed 780G Auto Mode with G4S sensor | Other | Approved | Diabetes type1 | COMPLETED | NCT05574062 |
| MiniMed 780G Auto Mode with DS5 sensor | Other | Approved | Diabetes type1 | COMPLETED | NCT05574062 |
| MiniMed 780G Manual Mode with G4S sensor | Other | Approved | Diabetes type1 | COMPLETED | NCT05574062 |
| MiniMed 780G Auto Mode with G4S sensor | Other | Approved | Diabetes type1 | COMPLETED | NCT05574062 |
| Pipeline™ Vantage Embolization Device with Shield Technology™ | Device | Approved | Intracranial Aneurysm | TERMINATED | NCT03873714 |
| Pipeline™ Vantage Embolization Device with Shield Technology™ | Device | Approved | Intracranial Aneurysm | TERMINATED | NCT03873714 |
| Focal Radiotherapy | Drug | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Temozolomide | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Ritonavir | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Lamivudine | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Abacavir | Other | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| Magnetic Resonance (MR)-guided Laser Interstitial Thermal Therapy (LITT) | Drug | Phase PHASE1 | High Grade Glioma | RECRUITING | NCT06428045 |
| MiniMed 780G System | Other | Approved | Type 1 Diabetes | COMPLETED | NCT05224258 |
| MiniMed 780G System | Other | Approved | Type 1 Diabetes | COMPLETED | NCT05224258 |
| MRI guided laser ablation | Other | Approved | Neoplasm Metastasis | RECRUITING | NCT05023772 |
| Stereotactic Radiosurgery | Procedure | Approved | Neoplasm Metastasis | RECRUITING | NCT05023772 |
| Stereotactic Laser Ablation | Other | Approved | Neoplasm Metastasis | RECRUITING | NCT05023772 |
| Implantable loop recorder | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03907982 |
| Pulmonary vein isolation | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03907982 |
| DC Cardioversion | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03907982 |
| Active biphasic pulse stimulation---Stimulator Off | Other | Approved | Essential Tremor | COMPLETED | NCT03811405 |
| Active biphasic pulse stimulation---VIN Biphasic | Other | Approved | Essential Tremor | COMPLETED | NCT03811405 |
| Active biphasic pulse stimulation---Home Settings | Other | Approved | Essential Tremor | COMPLETED | NCT03811405 |
| Electrophysiological Study | Other | Approved | Heart Failure | COMPLETED | NCT01883141 |
| Electrophysiological Study | Other | Approved | Heart Failure | COMPLETED | NCT01883141 |
| Electrophysiological Study | Other | Approved | Heart Failure | COMPLETED | NCT01883141 |
| Transient Loss of Consciousness (T-LOC) | Other | Preclinical | Brief Loss of Consciousness | COMPLETED | NCT01721369 |
| Transient Loss of Consciousness (T-LOC) | Other | Preclinical | Brief Loss of Consciousness | COMPLETED | NCT01721369 |
| Pacing system implant with the CapsureFix MRI pacing lead model 5086 | Other | Preclinical | Bradyarrhythmia | COMPLETED | NCT01522755 |
| TherapyGuide | Drug | Preclinical | Bradyarrhythmia | COMPLETED | NCT01513538 |
| CRT-P or CRT-D | Other | Approved | Heart Failure | COMPLETED | NCT01059175 |
| Additional Endocardial or Epicardial LV Lead | Other | Approved | Heart Failure | COMPLETED | NCT01059175 |
| Medtronic CareLink® Network | Other | Preclinical | Heart Failure | COMPLETED | NCT01023022 |
| Medtronic CareLink® Network | Other | Preclinical | Heart Failure | COMPLETED | NCT01023022 |
| Medtronic CareLink® Network | Other | Approved | Heart Failure | TERMINATED | NCT00885677 |
| Medtronic CareLink® Network | Other | Approved | Heart Failure | TERMINATED | NCT00885677 |
| Medtronic CareLink® Network | Other | Approved | Heart Failure | TERMINATED | NCT00885677 |
| Secura ICD | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00526227 |
| Secura ICD | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00526227 |
| Secura ICD | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00526227 |
| Bi-ventricular Implantable Cardioverter Defibrillator | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00526162 |
| Bi-ventricular Implantable Cardioverter Defibrillator | Other | Approved | Tachyarrhythmias | COMPLETED | NCT00526162 |
| Programming (CRT-D, ICD OptiVol® and Cardiac Compass® ) | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT00480077 |
| Programming (CRT-D, ICD OptiVol® and Cardiac Compass® ) | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT00480077 |
| Programming (CRT-D, ICD OptiVol® and Cardiac Compass® ) | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT00480077 |
| Blood sampling | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT00478933 |
| Defibrillator, Dual Chamber ; Implantable | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT00478933 |
| Blood sampling | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT00478933 |
| Defibrillator, Dual Chamber ; Implantable | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT00478933 |
| Blood sampling | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT00478933 |
| Defibrillator, Dual Chamber ; Implantable | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT00478933 |
| Pacemaker Medtronic EnRhythm | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00262119 |
| Pacemaker Medtronic EnRhythm | Other | Phase PHASE4 | Atrial Fibrillation | COMPLETED | NCT00262119 |
| Dual Chamber implantable cardioverter defibrilator | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00157820 |
| Single Chamber Implantable Cardioverter Defibrillator | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00157820 |
| Dual Chamber implantable cardioverter defibrilator | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00157820 |
| Single Chamber Implantable Cardioverter Defibrillator | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT00157820 |
| Implantable Cardiac Defibrillator | Other | Phase PHASE4 | Tachycardia, Ventricular | COMPLETED | NCT00147290 |
| Implantable Cardiac Defibrillator | Other | Phase PHASE4 | Tachycardia, Ventricular | COMPLETED | NCT00147290 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Valiant Navion Thoracic Stent Graft System | Other | Preclinical | Thoracic Aortic Dissection | COMPLETED | NCT04267055 |
| Valiant Navion Thoracic Stent Graft System | Other | Preclinical | Thoracic Aortic Dissection | COMPLETED | NCT04267055 |
| CareLinK | Other | Preclinical | Arrythmia | COMPLETED | NCT02401659 |
| CareLinK | Other | Preclinical | Arrythmia | COMPLETED | NCT02401659 |
| Melody valve implantation | Other | Preclinical | Right Ventricular Congenital Cardiopathies | COMPLETED | NCT02023775 |
| Melody valve implantation | Other | Preclinical | Right Ventricular Congenital Cardiopathies | COMPLETED | NCT02023775 |
| Fill out Questionnaire | Other | Phase PHASE4 | Bradycardia | COMPLETED | NCT01037426 |
| Fill out Questionnaire | Other | Phase PHASE4 | Bradycardia | COMPLETED | NCT01037426 |
| Intensive insulin infusion | Other | Approved | Acute Heart Failure | WITHDRAWN | NCT00922402 |
| Intensive insulin infusion | Other | Approved | Acute Heart Failure | WITHDRAWN | NCT00922402 |
| Implantable cardioverter defibrillator | Other | Phase PHASE4 | Acute Myocardial Infarction | COMPLETED | NCT00157768 |
| Implantable cardioverter defibrillator | Other | Phase PHASE4 | Acute Myocardial Infarction | COMPLETED | NCT00157768 |
| PTA | Other | Approved | Critical Limb Ischemia | COMPLETED | NCT02963649 |
| DCB | Other | Approved | Critical Limb Ischemia | COMPLETED | NCT02963649 |
| PTA | Other | Approved | Critical Limb Ischemia | COMPLETED | NCT02963649 |
| DCB | Other | Approved | Critical Limb Ischemia | COMPLETED | NCT02963649 |
| PTA | Other | Approved | Critical Limb Ischemia | COMPLETED | NCT02963649 |
| DCB | Other | Approved | Critical Limb Ischemia | COMPLETED | NCT02963649 |
| aCRT OFF | Other | Approved | Heart Failure | COMPLETED | NCT04180696 |
| aCRT ON | Other | Approved | Heart Failure | COMPLETED | NCT04180696 |
| Implantable Cardiac Defibrillator | Other | Phase PHASE4 | Tachycardia, Ventricular | COMPLETED | NCT00147277 |
| Implantable Cardiac Defibrillator | Other | Phase PHASE4 | Tachycardia, Ventricular | COMPLETED | NCT00147277 |
| Programmer ECG first | Other | Approved | Heart Failure | COMPLETED | NCT01297283 |
| LECG first | Other | Approved | Heart Failure | COMPLETED | NCT01297283 |
| Programmer ECG first | Other | Approved | Heart Failure | COMPLETED | NCT01297283 |
| LECG first | Other | Approved | Heart Failure | COMPLETED | NCT01297283 |
| Dual chamber pacemeker | Other | Phase PHASE4 | Syncope | COMPLETED | NCT00359203 |
| Dual chamber pacemeker | Other | Phase PHASE4 | Syncope | COMPLETED | NCT00359203 |
| Philips FAST SpO2 with Nellcor Pulse Oximetry Sensors | Other | Preclinical | Oxygen Saturation Measurement | COMPLETED | NCT06860230 |
| Philips FAST SpO2 with Nellcor Pulse Oximetry Sensors | Other | Preclinical | Oxygen Saturation Measurement | COMPLETED | NCT06860230 |
| Observational | Other | Preclinical | Oxygen Saturation | COMPLETED | NCT06581835 |
| Observational | Other | Preclinical | Oxygen Saturation | COMPLETED | NCT06581835 |
| Deep Brain Simulator | Other | Approved | Opioid-Related Disorders | ACTIVE_NOT_RECRUITING | NCT03950492 |
| Defibrillation using EV-ICD | Other | Preclinical | Ventricular Arrhythmia | ACTIVE_NOT_RECRUITING | NCT06048731 |
| Transorb™ Self-Gripping Resorbable Mesh | Other | Approved | Hernia | ACTIVE_NOT_RECRUITING | NCT06449378 |
| Transorb™ Self-Gripping Resorbable Mesh | Other | Approved | Hernia | ACTIVE_NOT_RECRUITING | NCT06449378 |
| Non-Interventional | Other | Preclinical | Atrial Fibrillation | TERMINATED | NCT04926857 |
| Non-Interventional | Other | Preclinical | Atrial Fibrillation | TERMINATED | NCT04926857 |
| Non-Interventional | Other | Preclinical | Atrial Fibrillation | TERMINATED | NCT04926857 |
| Liberal post-dilatation strategy during PCI | Other | Preclinical | Coronary Artery Disease | RECRUITING | NCT06558474 |
| Pedicle screw instrumentation using Mazor X robotic system | Device | Approved | Spinal Deformity | ACTIVE_NOT_RECRUITING | NCT05884593 |
| Valiant Mona LSA Thoracic Stent Graft System | Other | Preclinical | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | COMPLETED | NCT02365467 |
| Valiant Mona LSA Thoracic Stent Graft System | Other | Preclinical | Aortic Aneurysm, Thoracic, Chronic Type B Dissection | COMPLETED | NCT02365467 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04806516 |
| Summit RC+S System with ECoG Paddles | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04806516 |
| Subject's Current Diabetes Therapy | Drug | Approved | Type 1 Diabetes | COMPLETED | NCT02748018 |
| 670G and 770G Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02748018 |
| Subject's Current Diabetes Therapy | Drug | Approved | Type 1 Diabetes | COMPLETED | NCT02748018 |
| 670G and 770G Insulin Pump | Other | Approved | Type 1 Diabetes | COMPLETED | NCT02748018 |
| HeartWare Ventricular Assist Device | Device | Preclinical | Chronic Heart Failure | ACTIVE_NOT_RECRUITING | NCT03681210 |
| HeartWare Ventricular Assist Device | Device | Preclinical | Chronic Heart Failure | ACTIVE_NOT_RECRUITING | NCT03681210 |
| Sotalol | Other | Phase PHASE4 | Atrial Fibrillation | RECRUITING | NCT02347111 |
| Flecainide | Other | Phase PHASE4 | Atrial Fibrillation | RECRUITING | NCT02347111 |
| Thrombus Aspiration | Other | Approved | Myocardial Infarction | COMPLETED | NCT05307965 |
| Percutaneous Coronary Intervention | Other | Approved | Myocardial Infarction | COMPLETED | NCT05307965 |
| Retriever Thrombectomy | Other | Approved | Myocardial Infarction | COMPLETED | NCT05307965 |
| Medtronic CoreValve™ Evolut™ PRO System (Evolut™ PRO System) | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT03417011 |
| Medtronic CoreValve™ Evolut™ PRO System (Evolut™ PRO System) | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT03417011 |
| Medtronic CoreValve™ Evolut™ PRO System (Evolut™ PRO System) | Other | Preclinical | Aortic Valve Stenosis | COMPLETED | NCT03417011 |
| Fissios App | Other | Approved | Surgical Procedure, Unspecified | RECRUITING | NCT06732193 |
| On-site respiratory physiotherapy | Drug | Approved | Surgical Procedure, Unspecified | RECRUITING | NCT06732193 |
| Fissios App | Other | Approved | Surgical Procedure, Unspecified | RECRUITING | NCT06732193 |
| On-site respiratory physiotherapy | Drug | Approved | Surgical Procedure, Unspecified | RECRUITING | NCT06732193 |
| Magnetic Resonance Imaging (MRI) scan | Other | Approved | Bradycardia | COMPLETED | NCT00433654 |
| Implantable Pulse Generator (IPG) and Pacing Leads (wires) | Other | Approved | Bradycardia | COMPLETED | NCT00433654 |
| Magnetic Resonance Imaging (MRI) scan | Other | Approved | Bradycardia | COMPLETED | NCT00433654 |
| Implantable Pulse Generator (IPG) and Pacing Leads (wires) | Other | Approved | Bradycardia | COMPLETED | NCT00433654 |
| Magnetic Resonance Imaging (MRI) scan | Other | Approved | Bradycardia | COMPLETED | NCT00433654 |
| Implantable Pulse Generator (IPG) and Pacing Leads (wires) | Other | Approved | Bradycardia | COMPLETED | NCT00433654 |
| 3D HRAM | Other | Preclinical | Constipation | ENROLLING_BY_INVITATION | NCT06924957 |
| Angiography and ECG | Other | Approved | Heart Diseases | RECRUITING | NCT07110922 |
| Angiography only | Other | Approved | Heart Diseases | RECRUITING | NCT07110922 |
| Intraoperative Nerve Monitoring | Other | Preclinical | Intracranial Surgery | COMPLETED | NCT06637995 |
| Radiofrequency Ablation | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03643224 |
| Radiofrequency Ablation | Other | Approved | Persistent Atrial Fibrillation | COMPLETED | NCT03643224 |
| Inceptiv | Other | Approved | Low Back Pain | COMPLETED | NCT05177354 |
| Inceptiv | Other | Approved | Low Back Pain | COMPLETED | NCT05177354 |
| Cervical Interfacet Spacers | Other | Preclinical | Cervical Fusion | RECRUITING | NCT04041583 |
| surgery (any volume) and / or pharmaceuticals treatment initiated or planned or only dynamic observation, in accordance with current clinical guidelines | Drug | Approved | Brain Tumours | NOT_YET_RECRUITING | NCT07384884 |
| Sacral Neuromodulation | Other | Approved | Overactive Bladder | RECRUITING | NCT05200923 |
| Sacral Neuromodulation | Other | Approved | Overactive Bladder | RECRUITING | NCT05200923 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| Multi-Organ Denervation Gemini System | Other | Approved | Hypertension | RECRUITING | NCT06907147 |
| No intervention | Other | Preclinical | Heart Failure | RECRUITING | NCT06540521 |
| No intervention | Other | Preclinical | Heart Failure | RECRUITING | NCT06540521 |
| No intervention | Other | Preclinical | Heart Failure | RECRUITING | NCT06540521 |
| Navigation bronchoscopy | Other | Approved | Lung Nodule | COMPLETED | NCT04250194 |
| CT-Guided Biopsy | Other | Approved | Lung Nodule | COMPLETED | NCT04250194 |
| Heart Ultrasound | Other | Approved | Heart Failure | COMPLETED | NCT05646251 |
| Implantable SCS with Closed Loop mechanism | Other | Approved | Diabetic Peripheral Neuropathic Pain (DPN) | ENROLLING_BY_INVITATION | NCT07209514 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| IN.PACT™ AV Drug Coated Balloon (DCB) - Extended Cohort | Drug | Preclinical | Arteriovenous Fistula | ACTIVE_NOT_RECRUITING | NCT04543539 |
| IN.PACT™ AV Drug Coated Balloon (DCB) - Primary Cohort | Drug | Preclinical | Arteriovenous Fistula | ACTIVE_NOT_RECRUITING | NCT04543539 |
| Intrinsic Antitachycardia Pacing (iATP) Therapy | Drug | Preclinical | Ventricular Tachycardia | ACTIVE_NOT_RECRUITING | NCT04496518 |
| Observational | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT04489225 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Medtronic TAVR Systems | Other | Approved | Bicuspid Aortic Valve | ACTIVE_NOT_RECRUITING | NCT03635424 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| InsuLearn | Other | Approved | Type 1 Diabetes Mellitus | COMPLETED | NCT06411548 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Medtronic CoreValve® Evolut R System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Medtronic CoreValve® Evolut R System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Approved | Severe Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT01586910 |
| Reclaim™ DBS Therapy | Drug | Approved | Obsessive-Compulsive Disorder (OCD) | RECRUITING | NCT02773082 |
| 780G | Other | Approved | Diabetes (Insulin-requiring, Type 1 or Type 2) | NOT_YET_RECRUITING | NCT07227805 |
| NMX8 | Other | Approved | Diabetes (Insulin-requiring, Type 1 or Type 2) | NOT_YET_RECRUITING | NCT07227805 |
| 780G | Other | Approved | Diabetes (Insulin-requiring, Type 1 or Type 2) | NOT_YET_RECRUITING | NCT07227805 |
| NMX8 | Other | Approved | Diabetes (Insulin-requiring, Type 1 or Type 2) | NOT_YET_RECRUITING | NCT07227805 |
| Arctic Front™ Cardiac Cryoablation Catheter System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT05005949 |
| Arctic Front™ Cardiac Cryoablation Catheter System | Other | Preclinical | Persistent Atrial Fibrillation | ACTIVE_NOT_RECRUITING | NCT05005949 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Arctic Front™ Cardiac Cryoablation Catheter | Other | Preclinical | Paroxysmal Atrial Fibrillation | RECRUITING | NCT05227053 |
| Sham Procedure | Procedure | Approved | Hypertension | COMPLETED | NCT02439775 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | COMPLETED | NCT02439775 |
| Sham Procedure | Procedure | Approved | Hypertension | COMPLETED | NCT02439775 |
| Symplicity Spyral™ multi-electrode renal denervation system | Other | Approved | Hypertension | COMPLETED | NCT02439775 |
| Symplicity Spyral Renal Denervation System | Other | Preclinical | Resistant Hypertension | RECRUITING | NCT07081243 |
| Symplicity Spyral Renal Denervation System | Other | Preclinical | Resistant Hypertension | RECRUITING | NCT07081243 |
| Symplicity Spyral Renal Denervation System | Other | Preclinical | Resistant Hypertension | RECRUITING | NCT07081243 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | ACTIVE_NOT_RECRUITING | NCT05817318 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| Self-Gripping Resorbable Mesh | Other | Approved | Incisional Hernia | ACTIVE_NOT_RECRUITING | NCT05424484 |
| Enhanced Vitals Monitoring | Other | Approved | Surgery | RECRUITING | NCT06584825 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Medtronic CoreValve™ Evolut™ PRO System | Other | Approved | Severe, Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04982588 |
| Medtronic CoreValve™ Evolut™ PRO System | Other | Approved | Severe, Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04982588 |
| Mesh augmented reinforcement | Other | Approved | Incisional Hernia | TERMINATED | NCT03912662 |
| Mesh augmented reinforcement | Other | Approved | Incisional Hernia | TERMINATED | NCT03912662 |
| Haemorrhoid artery embolizsation (HAE) | Other | Preclinical | Hemorrhoid | NOT_YET_RECRUITING | NCT07264413 |
| Defibrillation (LBBAP Implant) | Other | Approved | Tachyarrhythmia | COMPLETED | NCT04863664 |
| Defibrillation (RV Implant) | Other | Approved | Tachyarrhythmia | COMPLETED | NCT04863664 |
| Defibrillation (LBBAP Implant) | Other | Approved | Tachyarrhythmia | COMPLETED | NCT04863664 |
| Defibrillation (RV Implant) | Other | Approved | Tachyarrhythmia | COMPLETED | NCT04863664 |
| Observation Only | Other | Approved | Subdural Hematoma | COMPLETED | NCT04402632 |
| Onyx™ Liquid Embolic System (LES) Embolization | Other | Approved | Subdural Hematoma | COMPLETED | NCT04402632 |
| Surgical Management | Other | Approved | Subdural Hematoma | COMPLETED | NCT04402632 |
| Observation Only | Other | Approved | Subdural Hematoma | COMPLETED | NCT04402632 |
| Onyx™ Liquid Embolic System (LES) Embolization | Other | Approved | Subdural Hematoma | COMPLETED | NCT04402632 |
| Surgical Management | Other | Approved | Subdural Hematoma | COMPLETED | NCT04402632 |
| SNM based on sacral evoked responses (SERs) | Other | Approved | Overactive Bladder | RECRUITING | NCT06983470 |
| SNM based on visual-motor responses (VMRs) | Other | Approved | Overactive Bladder | RECRUITING | NCT06983470 |
| Intensified GetReady application | Other | Approved | Obesity &Amp; Overweight | RECRUITING | NCT07297342 |
| GetReady application | Other | Approved | Obesity &Amp; Overweight | RECRUITING | NCT07297342 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Certain imaging assessments can be non-Standard of Care | Other | Approved | Severe Pulmonary Valve Regurgitation | RECRUITING | NCT06906926 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Deep Brain Stimulation System | Other | Preclinical | Dystonia | RECRUITING | NCT07309133 |
| Surgical Stripping | Other | Approved | Venous Reflux | TERMINATED | NCT03820947 |
| Endothermal Ablation (ETA) | Other | Approved | Venous Reflux | TERMINATED | NCT03820947 |
| VenaSeal™ System | Other | Approved | Venous Reflux | TERMINATED | NCT03820947 |
| Surgical Stripping | Other | Approved | Venous Reflux | TERMINATED | NCT03820947 |
| Endothermal Ablation (ETA) | Other | Approved | Venous Reflux | TERMINATED | NCT03820947 |
| VenaSeal™ System | Other | Approved | Venous Reflux | TERMINATED | NCT03820947 |
| Local and topical anesthesia | Other | Approved | Sinusitis | RECRUITING | NCT02975310 |
| General Anesthesia | Other | Approved | Sinusitis | RECRUITING | NCT02975310 |
| Endoscopic Sinus Surgery (ESS) | Procedure | Approved | Sinusitis | RECRUITING | NCT02975310 |
| Endoscopic polypectomy in clinic (EPIC) | Other | Approved | Sinusitis | RECRUITING | NCT02975310 |
| BIV-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| LB-CRT | Other | Approved | Left Ventricular Ejection Fraction | ACTIVE_NOT_RECRUITING | NCT05652218 |
| Ablation and Pacemaker Implantation | Other | Approved | HIS Bundle Pacing | RECRUITING | NCT06152406 |
| Wearable Gait Sensor Analysis | Other | Preclinical | Dystonia | RECRUITING | NCT07323602 |
| N/A observational registry | Other | Preclinical | Minimally Invasive Surgical Procedures | COMPLETED | NCT05095935 |
| Harmony TPV System | Other | Approved | Congenital Heart Disease | ACTIVE_NOT_RECRUITING | NCT05077774 |
| Harmony TPV System | Other | Approved | Congenital Heart Disease | ACTIVE_NOT_RECRUITING | NCT05077774 |
| Harmony TPV System | Other | Approved | Congenital Heart Disease | ACTIVE_NOT_RECRUITING | NCT05077774 |
| iPro2 Professional CGM | Other | Approved | T2DM (Type 2 Diabetes Mellitus) | TERMINATED | NCT03067480 |
| Closed-loop deep brain stimulation | Other | Approved | Essential Tremor | ACTIVE_NOT_RECRUITING | NCT02649166 |
| Deep brain stimulation | Other | Approved | Essential Tremor | ACTIVE_NOT_RECRUITING | NCT02649166 |
| Observational | Other | Preclinical | Tissue Oxygenation | ACTIVE_NOT_RECRUITING | NCT07166341 |
| Observational | Other | Preclinical | Tissue Oxygenation | ACTIVE_NOT_RECRUITING | NCT07166341 |
| Evolut™ PRO and Evolut™ PRO+ System (Evolut™ FX System for the addendum) | Other | Preclinical | Symptomatic Aortic Stenosis | COMPLETED | NCT04091048 |
| Evolut™ PRO and Evolut™ PRO+ System (Evolut™ FX System for the addendum) | Other | Preclinical | Symptomatic Aortic Stenosis | COMPLETED | NCT04091048 |
| Medtronic DBM | Other | Approved | Multi-Level Degenerative Lumbosacral Spinal Conditions | ACTIVE_NOT_RECRUITING | NCT03118505 |
| Infuse Bone Graft | Other | Approved | Multi-Level Degenerative Lumbosacral Spinal Conditions | ACTIVE_NOT_RECRUITING | NCT03118505 |
| Medtronic DBM | Other | Approved | Multi-Level Degenerative Lumbosacral Spinal Conditions | ACTIVE_NOT_RECRUITING | NCT03118505 |
| Infuse Bone Graft | Other | Approved | Multi-Level Degenerative Lumbosacral Spinal Conditions | ACTIVE_NOT_RECRUITING | NCT03118505 |
| FHC Guideline 4000+ system and/or Medtronic RC+S | Other | Preclinical | Essential Tremor | COMPLETED | NCT02712515 |
| Ad-Tech Medical Instrumentation Corp. electrodes/subdural strips | Device | Preclinical | Essential Tremor | COMPLETED | NCT02712515 |
| Deep brain stimulation implantation surgery | Procedure | Preclinical | Essential Tremor | COMPLETED | NCT02712515 |
| No intervention (observational study) | Other | Preclinical | Parkinson's Disease (PD) | RECRUITING | NCT07336199 |
| China market released 3.0T Magnetic resonance (MR) conditional CIED systems | Other | Approved | Bradycardia | COMPLETED | NCT06038123 |
| China market released 3.0T Magnetic resonance (MR) conditional CIED systems | Other | Approved | Bradycardia | COMPLETED | NCT06038123 |
| Commercially available neurostimulation systems | Other | Preclinical | Pain, Intractable | TERMINATED | NCT05775510 |
| Commercially available neurostimulation systems | Other | Preclinical | Pain, Intractable | TERMINATED | NCT05775510 |
| Medtronic Intrepid™ Transcatheter Transfemoral Mitral Valve Replacement System | Other | Approved | Mitral Valve Insufficiency | ACTIVE_NOT_RECRUITING | NCT02322840 |
| Twelve TMVR Implant | Other | Approved | Mitral Valve Insufficiency | ACTIVE_NOT_RECRUITING | NCT02322840 |
| Onyx Drug Eluting Stent group | Drug | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT02593994 |
| Onyx Drug Eluting Stent group | Drug | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT02593994 |
| Onyx Drug Eluting Stent group | Drug | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT02593994 |
| Medtronic SenSight Directional DBS lead | Other | Phase PHASE1 | Treatment Resistant Depression | RECRUITING | NCT06096207 |
| NA-Observational Registry | Other | Preclinical | Chronic Rhinosinusitis (Diagnosis) | COMPLETED | NCT05925985 |
| Implant procedure of a Micra AV2 leadless pacemaker (Medtronic) | Procedure | Approved | AV Block Complete | RECRUITING | NCT07356505 |
| Minimally invasive lumbar fusion | Other | Preclinical | Intervertebral Disc Degeneration | COMPLETED | NCT02617563 |
| Minimally invasive lumbar fusion | Other | Preclinical | Intervertebral Disc Degeneration | COMPLETED | NCT02617563 |
| Minimally invasive lumbar fusion | Other | Preclinical | Intervertebral Disc Degeneration | COMPLETED | NCT02617563 |
| Model 10642 Implantable Intravascular Catheter | Other | Approved | Pulmonary Arterial Hypertension | ACTIVE_NOT_RECRUITING | NCT01321073 |
| Objective-Guided DBS Programming (Imaging and Local Field Potential-Based) | Other | Approved | Parkinson's Disease | NOT_YET_RECRUITING | NCT07369310 |
| Conventional DBS Programming (Monopolar Review) | Other | Approved | Parkinson's Disease | NOT_YET_RECRUITING | NCT07369310 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pipeline™ Flex Embolization Device with Shield Technology™ | Device | Approved | Intracranial Aneurysm | TERMINATED | NCT04391803 |
| Pipeline™ Flex Embolization Device with Shield Technology™ | Device | Approved | Intracranial Aneurysm | TERMINATED | NCT04391803 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | RECRUITING | NCT04735016 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | RECRUITING | NCT04735016 |
| DiamondTemp™ Ablation System | Other | Preclinical | Arrhythmia | RECRUITING | NCT04735016 |
| Micra AV Transcatheter Pacing System | Other | Preclinical | Bradycardia | COMPLETED | NCT04253184 |
| Intervertebral body fusion device and Medtronic posterior Fixation Systems | Device | Approved | Degenerative Disease of the Lumbosacral Spine | ACTIVE_NOT_RECRUITING | NCT04073563 |
| Infuse™ Bone Graft (Infuse™) | Other | Approved | Degenerative Disease of the Lumbosacral Spine | ACTIVE_NOT_RECRUITING | NCT04073563 |
| Intervertebral body fusion device and Medtronic posterior Fixation Systems | Device | Approved | Degenerative Disease of the Lumbosacral Spine | ACTIVE_NOT_RECRUITING | NCT04073563 |
| Infuse™ Bone Graft (Infuse™) | Other | Approved | Degenerative Disease of the Lumbosacral Spine | ACTIVE_NOT_RECRUITING | NCT04073563 |
| Quadripolar LV Lead | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT04024943 |
| Micra Transcatheter Pacing System | Other | Preclinical | Bradycardia | ACTIVE_NOT_RECRUITING | NCT02536118 |
| 28-day non-invasive continuous ECG monitoring (patch) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04075500 |
| Subcutaneously implanted event recorder (REVEAL LINQ) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04075500 |
| 28-day non-invasive continuous ECG monitoring (patch) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04075500 |
| Subcutaneously implanted event recorder (REVEAL LINQ) | Other | Approved | Atrial Fibrillation | COMPLETED | NCT04075500 |
| traditional/standard insulin pen | Other | Approved | Diabetes Mellitus | RECRUITING | NCT06918977 |
| InPen Smart insulin pen | Other | Approved | Diabetes Mellitus | RECRUITING | NCT06918977 |
| ipsilateral VO | Other | Approved | Essential Tremor | RECRUITING | NCT04212780 |
| standard ET DBS | Other | Approved | Essential Tremor | RECRUITING | NCT04212780 |
| ipsilateral thalamic (VIM+VO) DBS | Other | Approved | Essential Tremor | RECRUITING | NCT04212780 |
| Medtronic Summit Rechargable (RC)+S | Other | Approved | Essential Tremor | RECRUITING | NCT04212780 |
| myPACE+ algorithm | Other | Approved | Non-obstructive Hypertrophic Cardiomyopathy | TERMINATED | NCT06775886 |
| Emprint Microwave Ablation System | Other | Preclinical | Colorectal Neoplasms Malignant | COMPLETED | NCT03775980 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| Edwards TAV | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06777368 |
| Medtronic TAV | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06777368 |
| Edwards TAV | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06777368 |
| Medtronic TAV | Other | Preclinical | Aortic Stenosis | RECRUITING | NCT06777368 |
| SpherePVI™ Catheter | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05144503 |
| SpherePVI™ Catheter | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05144503 |
| SpherePVI™ Catheter | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05115214 |
| SpherePVI™ Catheter | Other | Approved | Atrial Fibrillation | RECRUITING | NCT05115214 |
| ICBG | Other | Approved | Disc Degeneration | NOT_YET_RECRUITING | NCT07414745 |
| MDT-0123 | Other | Approved | Disc Degeneration | NOT_YET_RECRUITING | NCT07414745 |
| ICBG | Other | Approved | Disc Degeneration | NOT_YET_RECRUITING | NCT07414745 |
| MDT-0123 | Other | Approved | Disc Degeneration | NOT_YET_RECRUITING | NCT07414745 |
| Edwards SAPIEN 3 or SAPIEN 3 Ultra THV Systems | Other | Approved | Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04722250 |
| Medtronic Evolut PRO, Evolut PRO+ or Evolut FX (where commercially available) TAV Systems | Other | Approved | Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04722250 |
| Edwards SAPIEN 3 or SAPIEN 3 Ultra THV Systems | Other | Approved | Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04722250 |
| Medtronic Evolut PRO, Evolut PRO+ or Evolut FX (where commercially available) TAV Systems | Other | Approved | Symptomatic Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT04722250 |
| Index or spine revision surgery for complex adult spinal deformity | Procedure | Preclinical | Adult Spinal Deformity | RECRUITING | NCT04194138 |
| Medtronic 780G AID | Other | Approved | Type 1 Diabetes | RECRUITING | NCT07287943 |
| Deep Brain Stimulation Model 3387 Model 3389 | Other | Approved | Major Depressive Disorder | ACTIVE_NOT_RECRUITING | NCT02046330 |
| Transcutaneous Carbon Dioxide Monitoring | Other | Preclinical | Neonatal Encephalopathy | ACTIVE_NOT_RECRUITING | NCT04603547 |
| Treatment arm | Drug | Approved | Cardiovascular Diseases | TERMINATED | NCT04172883 |
| Treatment arm | Drug | Approved | Cardiovascular Diseases | TERMINATED | NCT04172883 |
| fecal immunological test (FIT) | Other | Preclinical | Colon Cancer | COMPLETED | NCT02738359 |
| colon capsule endoscopy | Other | Preclinical | Colon Cancer | COMPLETED | NCT02738359 |
| optical colonoscopy | Other | Preclinical | Colon Cancer | COMPLETED | NCT02738359 |
| Valiant PS-IDE Stent Graft | Other | Approved | Dissection of Thoracic Aorta | TERMINATED | NCT03322033 |
| Sacral Neuromodulation | Other | Approved | Overactive Bladder | RECRUITING | NCT05200923 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | NOT_YET_RECRUITING | NCT07335341 |
| Liberant Thrombectomy System | Other | Preclinical | Venous Embolism of Lower Extremities (Diagnosis) | NOT_YET_RECRUITING | NCT07335341 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia (VT) | RECRUITING | NCT06703489 |
| Sphere-9 Catheter with the Affera Mapping and Ablation System | Other | Approved | Ventricular Tachycardia (VT) | RECRUITING | NCT06703489 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Cardioblate and Cryoflex hand held devices | Device | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Surgical Ablation | Other | Approved | Persistent Atrial Fibrillation | RECRUITING | NCT03546374 |
| Robotic Assisted-Surgery (RAS) Hysterectomy | Procedure | Approved | Uterine Fibroids (UF) | RECRUITING | NCT07120945 |
| Robotic Assisted-Surgery (RAS) Hysterectomy | Procedure | Approved | Uterine Fibroids (UF) | RECRUITING | NCT07120945 |
| Automated alert | Other | Approved | Aortic Valve Stenosis | COMPLETED | NCT06099665 |
| embolization of middle meningeal arteries | Other | Approved | Migraine | NOT_YET_RECRUITING | NCT07223008 |
| Percept™ PC and Percept RC with Adaptive DBS (aDBS™) | Other | Approved | Parkinson's Disease | RECRUITING | NCT07216976 |
| Percept™ PC and Percept RC with Adaptive DBS (aDBS™) | Other | Approved | Parkinson's Disease | RECRUITING | NCT07216976 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | RECRUITING | NCT07408141 |
| MiniMed Fit Payload adhesive components | Other | Preclinical | Diabetes (Insulin-requiring, Type 1 or Type 2) | RECRUITING | NCT07408141 |
| 1041PTS (or similar) Kendall™ Neonatal Electrodes with IntelliVue MP5 Portable Patient Monitor | Other | Preclinical | Newborn | COMPLETED | NCT06637917 |
| LNCS® NEO SpO2 Sensor with RAD-97™ Pulse CO-Oximeter | Other | Preclinical | Newborn | COMPLETED | NCT06637917 |
| OxySoftN™ Neonatal-Adult SpO2 Sensor with N600X Nellcor™ Patient Monitoring System | Other | Preclinical | Newborn | COMPLETED | NCT06637917 |
| 1041PTS (or similar) Kendall™ Neonatal Electrodes with IntelliVue MP5 Portable Patient Monitor | Other | Preclinical | Newborn | COMPLETED | NCT06637917 |
| LNCS® NEO SpO2 Sensor with RAD-97™ Pulse CO-Oximeter | Other | Preclinical | Newborn | COMPLETED | NCT06637917 |
| OxySoftN™ Neonatal-Adult SpO2 Sensor with N600X Nellcor™ Patient Monitoring System | Other | Preclinical | Newborn | COMPLETED | NCT06637917 |
| Signia™ circular stapler with Tri-Staple™ Technology (Signia™ Circular Stapling system) | Other | Approved | Colorectal Anastomosis | RECRUITING | NCT07351071 |
| Signia™ circular stapler with Tri-Staple™ Technology (Signia™ Circular Stapling system) | Other | Approved | Colorectal Anastomosis | RECRUITING | NCT07351071 |
| endosuture aneurysm repair (ESAR) using Heli-FX EndoAnchor system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| endovascular aneurysm repair (EVAR) using the Endurant II/IIs stent graft system | Other | Approved | Aortic Aneurysm, Abdominal | RECRUITING | NCT05484115 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT) | Drug | Approved | Moderate Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT05149755 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Artisse™ Intrasaccular Device | Device | Approved | Intracranial Aneurysm | RECRUITING | NCT02998229 |
| Medtronic Summit System, Olympus | Other | Approved | Epilepsy | ACTIVE_NOT_RECRUITING | NCT03946618 |
| cDBS | Other | Approved | Parkinson Disease | COMPLETED | NCT07106242 |
| Adaptive DBS | Other | Approved | Parkinson Disease | COMPLETED | NCT07106242 |
| cDBS | Other | Approved | Parkinson Disease | COMPLETED | NCT07106242 |
| Adaptive DBS | Other | Approved | Parkinson Disease | COMPLETED | NCT07106242 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Surgical Aortic Valve Replacement (SAVR) | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Medtronic Transcatheter Aortic Valve Replacement Systems | Other | Approved | Aortic Valve Stenosis | ACTIVE_NOT_RECRUITING | NCT02701283 |
| Braive™ Growth Modulation System (Braive™ GMS) | Other | Approved | Juvenile Idiopathic Scoliosis | TERMINATED | NCT04929678 |
| Braive™ Growth Modulation System (Braive™ GMS) | Other | Approved | Juvenile Idiopathic Scoliosis | TERMINATED | NCT04929678 |
| Implantable Insulin Pump System | Other | Approved | Type I Diabetes | RECRUITING | NCT06739811 |
| Implantable Insulin Pump System | Other | Approved | Type I Diabetes | RECRUITING | NCT06739811 |
| EndoFLIP | Other | Approved | Esophagogastric Junction Distensibility | ACTIVE_NOT_RECRUITING | NCT04450628 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| PulseSelect™ PFA system | Other | Preclinical | Atrial Fibrillation | RECRUITING | NCT06578104 |
| Pulmonary Vein Isolation | Other | Approved | Atrial Fibrillation | TERMINATED | NCT04282850 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Personalized cardiac pacing | Other | Approved | Heart Failure With Preserved Ejection Fraction (HFpEF) | RECRUITING | NCT06678841 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Medtronic Intrepid Transcatheter Mitral Valve Replacement System (TMVR) | Other | Approved | Mitral Valve Regurgitation | RECRUITING | NCT03242642 |
| Commercially available Inceptiv™ neurostimulation systems | Other | Preclinical | Chronic Pain | NOT_YET_RECRUITING | NCT07507422 |
| Standard Postoperative Care plus In-Bed Cycling | Other | Approved | Spine | RECRUITING | NCT07506720 |
| Standard Postoperative Care plus In-Bed Cycling | Other | Approved | Spine | RECRUITING | NCT07506720 |
| Standard Postoperative Care plus In-Bed Cycling | Other | Approved | Spine | RECRUITING | NCT07506720 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Medtronic CoreValve® System Transcatheter Aortic Valve Implantation (TAVI) | Other | Preclinical | Severe Aortic Stenosis | COMPLETED | NCT01675440 |
| Conservative management | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Surgical explantation and aortic valve replacement | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| Any commercially available Edwards or Medtronic transcatheter aortic valve with the TAV-in-TAV (Redo TAVI) indication | Other | Preclinical | Aortic Valve Stenosis | RECRUITING | NCT06557798 |
| DiamondTemp™ Ablation System | Other | Preclinical | Paroxysmal Atrial Fibrillation | TERMINATED | NCT05230524 |
| DiamondTemp™ Ablation System | Other | Preclinical | Paroxysmal Atrial Fibrillation | TERMINATED | NCT05230524 |
| DiamondTemp™ Ablation System | Other | Preclinical | Paroxysmal Atrial Fibrillation | TERMINATED | NCT05230524 |
| Resolute Onyx Stent | Other | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| Resolute Integrity Stent | Other | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| CABG | Other | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| FFR guided PCI | Other | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| Gore Excluder or Gore/ Excluder Conformable AAA Endoprosthesis | Other | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Medtronic Endurant II or Endurant IIs Stent Graft System | Other | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Gore Excluder or Gore/ Excluder Conformable AAA Endoprosthesis | Other | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Medtronic Endurant II or Endurant IIs Stent Graft System | Other | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Gore Excluder or Gore/ Excluder Conformable AAA Endoprosthesis | Other | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Medtronic Endurant II or Endurant IIs Stent Graft System | Other | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Balloon catheter | Other | Approved | ST-segment Elevation Myocardial Infarction (STEMI) | ACTIVE_NOT_RECRUITING | NCT05510661 |
| Export Catheter | Other | Approved | ST-segment Elevation Myocardial Infarction (STEMI) | ACTIVE_NOT_RECRUITING | NCT05510661 |
| Sphere-9 Catheter Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07298473 |
| Sphere-9 Catheter Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07298473 |
| Sphere-9 Catheter Ablation | Other | Approved | Atrial Fibrillation (AF) | RECRUITING | NCT07298473 |
| Surgical Heart Valve Replacement Products | Other | Preclinical | Valve Disease, Heart | RECRUITING | NCT04073420 |
| Surgical Heart Valve Repair Products | Other | Preclinical | Valve Disease, Heart | RECRUITING | NCT04073420 |
| Surgical Heart Valve Replacement Products | Other | Preclinical | Valve Disease, Heart | RECRUITING | NCT04073420 |
| Surgical Heart Valve Repair Products | Other | Preclinical | Valve Disease, Heart | RECRUITING | NCT04073420 |
| Electrical isolation of pulmonary veins | Other | Approved | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | COMPLETED | NCT01490814 |
| Electrical isolation of the pulmonary veins | Other | Approved | Symptomatic Paroxysmal Atrial Fibrillation (PAF) | COMPLETED | NCT01490814 |
| Tacticath/Tactiflex (TF) ablation catheter | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT06028919 |
| Temperature controlled DiamondTemp (DT) ablation catheter | Other | Approved | Ventricular Tachycardia | COMPLETED | NCT06028919 |
| endovascular treament | Other | Preclinical | Aortic Aneurysm | COMPLETED | NCT01534819 |
| EndoAnchor™ | Other | Preclinical | Aortic Aneurysm | COMPLETED | NCT01534819 |
| endovascular treament | Other | Preclinical | Aortic Aneurysm | COMPLETED | NCT01534819 |
| EndoAnchor™ | Other | Preclinical | Aortic Aneurysm | COMPLETED | NCT01534819 |
| MaxTack™ Motorized Fixation Device | Device | Approved | Ventral Hernia | ACTIVE_NOT_RECRUITING | NCT06710795 |
| MaxTack™ Motorized Fixation Device | Device | Approved | Ventral Hernia | ACTIVE_NOT_RECRUITING | NCT06710795 |
| MiniMed™ 780G Insulin Pump system | Other | Approved | Type 2 Diabetes Treated With Insulin | COMPLETED | NCT05238142 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Right Ventricular Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Left Bundle Branch Area Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Observational | Other | Preclinical | Bradycardia Sinus | ACTIVE_NOT_RECRUITING | NCT06910059 |
| Penditure™ Left Atrial Appendage (LAA) Exclusion System | Other | Approved | Left Atrial Appendage Exclusion | ACTIVE_NOT_RECRUITING | NCT06203054 |
| Right Ventricular Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Left Bundle Branch Area Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Normal Subcutaneous Tissue | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Lipohypertrophy | Other | Approved | Diabetes Mellitus | TERMINATED | NCT02748434 |
| Renal Denervation | Other | Approved | Arrhythmia Burden in Patients With Recurrent, Paroxysmal Atrial Fibrillation Despite Durable Pulmonary Vein Isolation | TERMINATED | NCT05817318 |
| Onyx™ Liquid Embolic System | Other | Approved | Peripheral Arterial Hemorrhage | RECRUITING | NCT06742801 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| Right Ventricular Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Left Bundle Branch Area Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| Right Ventricular Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Left Bundle Branch Area Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Right Ventricular Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Left Bundle Branch Area Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Right Ventricular Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Left Bundle Branch Area Pacemaker | Other | Approved | Left Bundle Branch Area Pacing | ACTIVE_NOT_RECRUITING | NCT05869500 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Bi-ventricular pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| Conduction system pacing | Other | Preclinical | Heart Failure | ACTIVE_NOT_RECRUITING | NCT06606288 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| Model 400 aortic valve bioprosthesis | Other | Approved | Aortic Stenosis | ACTIVE_NOT_RECRUITING | NCT02088554 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| LOT-CRT | Other | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| LBBAP Therapy | Drug | Approved | Heart Failure | NOT_YET_RECRUITING | NCT07526896 |
| NMX8 System - Control Arm | Other | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| AID Therapy | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| NMX8 System - Treatment arm | Drug | Approved | Type 1 Diabetes (T1D) | NOT_YET_RECRUITING | NCT07401901 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| One Month Blinded Discontinuation Period | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Activa PC+S DBS implant for OCD | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT03457675 |
| Laser doppler vibrometry | Other | Approved | Resistant Hypertension | ACTIVE_NOT_RECRUITING | NCT07207226 |
| defibrillation lead | Other | Preclinical | Tachyarrhythmia | ENROLLING_BY_INVITATION | NCT07005232 |
| Medtronic Renal Denervation System | Other | Preclinical | Hypertension | RECRUITING | NCT01534299 |
| Pacemaker non-pacing mode or an exertional rate-adaptive pacing mode with no planned pacing at rest. | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Pacemaker PLR + TRT ON | Other | Approved | Heart Failure With Preserved Ejection Fraction | RECRUITING | NCT05839730 |
| Distal gastric bypass | Other | Approved | Obesity, Morbid | RECRUITING | NCT04894838 |
| Rivaroxaban | Other | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| One Month Blinded Discontinuation Period: | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Summit RC+S System | Other | Approved | Obsessive-Compulsive Disorder | ACTIVE_NOT_RECRUITING | NCT04281134 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| Agent DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| Prevail DCB | Other | Approved | Coronary Artery Disease | RECRUITING | NCT06535854 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| Optical coherence tomography-guided Onyx family stent expansion | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Optical coherence tomography-guided percutaneous coronary intervention | Other | Preclinical | Coronary Artery Disease | ACTIVE_NOT_RECRUITING | NCT05340361 |
| Treatment for Acute Ischemic Stroke | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Treatment for intracranial aneurysms | Drug | Preclinical | Intracranial Aneurysm | RECRUITING | NCT02988128 |
| Activa™ PC and Percept™ PC Neurostimulation Systems | Other | Approved | Epilepsy | TERMINATED | NCT03900468 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| kyphoplasty with Osteocool | Other | Preclinical | Thoracic Neoplasms | RECRUITING | NCT07479199 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| RAAP | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP off | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| BBAP on | Other | Approved | Heart Failure and Reduced Ejection Fraction | NOT_YET_RECRUITING | NCT07547306 |
| None, observational standard of care study | Other | Preclinical | Chronic Rhinosinusitis (CRS) | RECRUITING | NCT07546682 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Renal Denervation (Symplicity Spyral™) | Other | Approved | Hypertension | ACTIVE_NOT_RECRUITING | NCT05198674 |
| Resolute Integrity™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03466151 |
| Renal Denervation (Symplicity Spyral™) | Other | Preclinical | Hypertension | RECRUITING | NCT07174622 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Medtronic Avalus Ultra | Other | Approved | Aortic Valve Disease | ACTIVE_NOT_RECRUITING | NCT06506903 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| Resolute Onyx™ Zotarolimus-Eluting Coronary Stent System | Other | Approved | Ischemic Heart Disease | ACTIVE_NOT_RECRUITING | NCT03471845 |
| MiniMed™ 780G Insulin Pump system | Other | Approved | Type 2 Diabetes Treated With Insulin | COMPLETED | NCT05238142 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Deactivated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| Medtronic Astra/Azure DR MRI IPG with AVIM therapy Activated | Drug | Approved | Hypertension | RECRUITING | NCT06059638 |
| MaxTack™ Motorized Fixation Device | Device | Approved | Ventral Hernia | ACTIVE_NOT_RECRUITING | NCT06710795 |
| MiniMed™ 780G Insulin Pump system | Other | Approved | Type 2 Diabetes Treated With Insulin | COMPLETED | NCT05238142 |
| MaxTack™ Motorized Fixation Device | Device | Approved | Ventral Hernia | ACTIVE_NOT_RECRUITING | NCT06710795 |
| MiniMed™ 780G Insulin Pump system | Other | Approved | Type 2 Diabetes Treated With Insulin | COMPLETED | NCT05238142 |
| MaxTack™ Motorized Fixation Device | Device | Approved | Ventral Hernia | ACTIVE_NOT_RECRUITING | NCT06710795 |
| MaxTack™ Motorized Fixation Device | Device | Approved | Ventral Hernia | ACTIVE_NOT_RECRUITING | NCT06710795 |
| placebo | DRUG | Phase PHASE2 | Crohns Disease | UNKNOWN | NCT00731172 |
| glatiramer acetate | DRUG | Phase PHASE2 | Crohns Disease | UNKNOWN | NCT00731172 |
| Adalimumab | DRUG | Phase PHASE4 | Spondyloarthritis | COMPLETED | NCT01174186 |
| Solitaire™ FR device | DEVICE | Preclinical | Stroke, Acute | COMPLETED | NCT01327989 |
| Sham procedure plus anti-secretory medication | DEVICE | Approved | Barrett Esophagus | COMPLETED | NCT00282672 |
| Ablation System plus anti-secretory medication | DEVICE | Approved | Barrett Esophagus | COMPLETED | NCT00282672 |
| Autogenous bone graft from tibia or iliac crest | PROCEDURE | Approved | Alveolar Bone Loss in Mandible | WITHDRAWN | NCT01308996 |
| INFUSE® Bone Graft | DEVICE | Preclinical | Alveolar Bone Loss | TERMINATED | NCT00991965 |
| Propofol | DRUG | Phase PHASE4 | Delayed Emergence From Anesthesia | COMPLETED | NCT02631525 |
| Desflurane | DRUG | Phase PHASE4 | Delayed Emergence From Anesthesia | COMPLETED | NCT02631525 |
| Routine care | OTHER | Phase PHASE3 | Stroke | COMPLETED | NCT00789542 |
| Intermittent Pneumatic compression | DEVICE | Phase PHASE3 | Stroke | COMPLETED | NCT00789542 |
| Bi-ventricular pacing | DEVICE | Approved | Atrioventricular Block, Second and Third Degree | UNKNOWN | NCT05553626 |
| Left bundle branch pacing | DEVICE | Approved | Atrioventricular Block, Second and Third Degree | UNKNOWN | NCT05553626 |
| A-V Impulse compression | DEVICE | Approved | Edema | COMPLETED | NCT01389089 |
| Multi-layer compression bandage | OTHER | Approved | Edema | COMPLETED | NCT01389089 |
| ice gel pack | BEHAVIORAL | Approved | Edema | COMPLETED | NCT01389089 |
| TRUFILL | DEVICE | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| Onyx | DEVICE | Phase PHASE2 | Brain Arteriovenous Malformations | COMPLETED | NCT00857662 |
| Rivaroxaban | DRUG | Approved | Atrial Fibrillation | RECRUITING | NCT06216769 |
| Transcatheter aortic valve implantation | DEVICE | Approved | Aortic Valve Stenosis | RECRUITING | NCT06874465 |
| Braive™ Growth Modulation System (Braive™ GMS) | DEVICE | Approved | Juvenile Idiopathic Scoliosis | ACTIVE_NOT_RECRUITING | NCT04929678 |
| DiamondTemp™ Ablation System | DEVICE | Preclinical | Paroxysmal Atrial Fibrillation | TERMINATED | NCT05230524 |
| Gore Excluder or Gore/ Excluder Conformable AAA Endoprosthesis | DEVICE | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Medtronic Endurant II or Endurant IIs Stent Graft System | DEVICE | Approved | Abdominal Aortic Aneurysm | RECRUITING | NCT05378347 |
| Resolute Onyx Stent | DEVICE | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| Resolute Integrity Stent | DEVICE | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| CABG | PROCEDURE | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| FFR guided PCI | PROCEDURE | Approved | Coronary Disease | COMPLETED | NCT02100722 |
| Professional continuous glucose monitoring (CGM) sensor (iPro™2) | DEVICE | Approved | Diabetes Mellitus, Type 2 | COMPLETED | NCT04667728 |
Total products: 3928