| Symbol | SYK |
|---|---|
| Name | STRYKER CORP |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Surgical & Medical Instruments & Apparatus |
| Address | 1941 STRYKER WAY, PORTAGE, MI 49002 |
| Telephone | 2693852600 |
| Fax | — |
| — | |
| Website | https://www.stryker.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0000310764 |
| Description | Stryker designs, manufactures, and markets an array of medical equipment, instruments, consumable supplies, and implantable devices. The product portfolio includes hip and knee replacements, endoscopy systems, operating room equipment, embolic coils, hospital beds and gurneys, and spinal devices. Stryker remains one of the three largest competitors in reconstructive orthopedic implants and holds the leadership position in operating room equipment. Nearly one fourth of Strykers total revenue currently comes from outside the United States. Additional info from NASDAQ: |
2026-06-24 12:03
Stryker partners with professional golfer Shane Lowry to spotlight the caregiver journey in joint replacement
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2026-06-02 20:24
Stiles Spencer S 🔴 sold 1.6K shares of STRYKER CORP (SYK) Transaction Date: Jun 01, 2026 | Filing ID: 000009
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2026-06-02 13:03
Stryker launches TPX HD® power tool, supporting demanding orthopaedic procedures
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2026-05-29 20:59
Fletcher Robert S 🔴 sold 4.5K shares of STRYKER CORP (SYK) at $310.22 ($1.4M) Transaction Date: May 28, 2026 | Filing ID: 000004
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2026-05-28 21:22
Director STRYKER RONDA E 🔴 sold 310.0K shares of STRYKER CORP (SYK) at $315.11 ($96.8M) Transaction Date: May 26, 2026 | Filing ID: 000008
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2026-05-28 20:48
📋 Fletcher Robert S (Officer) plans to sell 5K shares of STRYKER CORP (at $305.59 each, total $1.4M) Filed: May 28, 2026 | ID: 000602
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2026-05-27 12:49
📋 STRYKER RONDA E (Director) plans to sell 310K shares of STRYKER CORP (at $313.00 each, total $97.0M) Filed: May 26, 2026 | ID: 000007
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2026-05-26 20:27
Stryker lanceert Pangea Plating System en voltooit de eerste case in Europa
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2026-05-26 20:27
Stryker bringt das Pangea-Plattensystem auf den Markt und schließt den ersten Eingriff in Europa ab
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2026-05-26 06:10
Stryker Launches Pangea Plating System and Completes First Case in Europe
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT00951145 | Medium and Long Term Outcome of Total Hip Arthroplasty Using Accolade TMZF Femo… | — | Osteoarthritis of the Hip | Unknown | — | — | ClinicalTrials.gov |
| NCT00951145 | Medium and Long Term Outcome of Total Hip Arthroplasty Using Accolade TMZF Femo… | — | Osteoarthritis of the Hip | Unknown | — | — | ClinicalTrials.gov |
| NCT00951145 | Medium and Long Term Outcome of Total Hip Arthroplasty Using Accolade TMZF Femo… | — | Osteoarthritis of the Hip | Unknown | — | — | ClinicalTrials.gov |
| NCT00951145 | Medium and Long Term Outcome of Total Hip Arthroplasty Using Accolade TMZF Femo… | — | Osteoarthritis of the Hip | Unknown | — | — | ClinicalTrials.gov |
| NCT00951145 | Medium and Long Term Outcome of Total Hip Arthroplasty Using Accolade TMZF Femo… | — | Osteoarthritis of the Hip | Unknown | — | — | ClinicalTrials.gov |
| NCT00951145 | Medium and Long Term Outcome of Total Hip Arthroplasty Using Accolade TMZF Femo… | — | Osteoarthritis of the Hip | Unknown | — | — | ClinicalTrials.gov |
| NCT07371091 | Post-market Clinical Investigation Plan: Collagen Dura Regeneration Membrane - … | — | Repair of Dura Mater | Not_Yet_Recruiting | 2026-07-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07371091 | Post-market Clinical Investigation Plan: Collagen Dura Regeneration Membrane - … | — | Repair of Dura Mater | Not_Yet_Recruiting | 2026-07-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07371091 | Post-market Clinical Investigation Plan: Collagen Dura Regeneration Membrane - … | — | Repair of Dura Mater | Not_Yet_Recruiting | 2026-07-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07371091 | Post-market Clinical Investigation Plan: Collagen Dura Regeneration Membrane - … | — | Repair of Dura Mater | Not_Yet_Recruiting | 2026-07-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07371091 | Post-market Clinical Investigation Plan: Collagen Dura Regeneration Membrane - … | — | Repair of Dura Mater | Not_Yet_Recruiting | 2026-07-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07371091 | Post-market Clinical Investigation Plan: Collagen Dura Regeneration Membrane - … | — | Repair of Dura Mater | Not_Yet_Recruiting | 2026-07-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT07647354 | Mako-MORE Registry | — | Arthropathy of Knee | Not_Yet_Recruiting | 2026-06-15 | 2037-03-15 | ClinicalTrials.gov |
| NCT07647354 | Mako-MORE Registry | — | Arthropathy of Knee | Not_Yet_Recruiting | 2026-06-15 | 2037-03-15 | ClinicalTrials.gov |
| NCT07647354 | Mako-MORE Registry | — | Arthropathy of Knee | Not_Yet_Recruiting | 2026-06-15 | 2037-03-15 | ClinicalTrials.gov |
| NCT07647354 | Mako-MORE Registry | — | Arthropathy of Knee | Not_Yet_Recruiting | 2026-06-15 | 2037-03-15 | ClinicalTrials.gov |
| NCT07647354 | Mako-MORE Registry | — | Arthropathy of Knee | Not_Yet_Recruiting | 2026-06-15 | 2037-03-15 | ClinicalTrials.gov |
| NCT07647354 | Mako-MORE Registry | — | Arthropathy of Knee | Not_Yet_Recruiting | 2026-06-15 | 2037-03-15 | ClinicalTrials.gov |
| NCT07392333 | A Prospective Cohort Study of Basivertebral Nerve Ablation Using the Stryker Op… | — | Verteborgenic Low Back Pain | Recruiting | 2026-06-02 | 2027-11-30 | ClinicalTrials.gov |
| NCT07392333 | A Prospective Cohort Study of Basivertebral Nerve Ablation Using the Stryker Op… | — | Verteborgenic Low Back Pain | Recruiting | 2026-06-02 | 2027-11-30 | ClinicalTrials.gov |
| NCT07392333 | A Prospective Cohort Study of Basivertebral Nerve Ablation Using the Stryker Op… | — | Verteborgenic Low Back Pain | Recruiting | 2026-06-02 | 2027-11-30 | ClinicalTrials.gov |
| NCT07392333 | A Prospective Cohort Study of Basivertebral Nerve Ablation Using the Stryker Op… | — | Verteborgenic Low Back Pain | Recruiting | 2026-06-02 | 2027-11-30 | ClinicalTrials.gov |
| NCT07392333 | A Prospective Cohort Study of Basivertebral Nerve Ablation Using the Stryker Op… | — | Verteborgenic Low Back Pain | Recruiting | 2026-06-02 | 2027-11-30 | ClinicalTrials.gov |
| NCT07392333 | A Prospective Cohort Study of Basivertebral Nerve Ablation Using the Stryker Op… | — | Verteborgenic Low Back Pain | Recruiting | 2026-06-02 | 2027-11-30 | ClinicalTrials.gov |
| NCT06660186 | Sternal Plating High Risk | Na | Heart Diseases | Recruiting | 2026-03-12 | 2027-06-30 | ClinicalTrials.gov |
| NCT06660186 | Sternal Plating High Risk | Na | Heart Diseases | Recruiting | 2026-03-12 | 2027-06-30 | ClinicalTrials.gov |
| NCT06660186 | Sternal Plating High Risk | Na | Heart Diseases | Recruiting | 2026-03-12 | 2027-06-30 | ClinicalTrials.gov |
| NCT06660186 | Sternal Plating High Risk | Na | Heart Diseases | Recruiting | 2026-03-12 | 2027-06-30 | ClinicalTrials.gov |
| NCT06660186 | Sternal Plating High Risk | Na | Heart Diseases | Recruiting | 2026-03-12 | 2027-06-30 | ClinicalTrials.gov |
| NCT06660186 | Sternal Plating High Risk | Na | Heart Diseases | Recruiting | 2026-03-12 | 2027-06-30 | ClinicalTrials.gov |
| NCT06929871 | Mako Cementless TKA vs Mako Cemented TKA | Na | Total Knee Replacement | Recruiting | 2025-09-29 | 2031-08-01 | ClinicalTrials.gov |
| NCT06929871 | Mako Cementless TKA vs Mako Cemented TKA | Na | Total Knee Replacement | Recruiting | 2025-09-29 | 2031-08-01 | ClinicalTrials.gov |
| NCT06929871 | Mako Cementless TKA vs Mako Cemented TKA | Na | Total Knee Replacement | Recruiting | 2025-09-29 | 2031-08-01 | ClinicalTrials.gov |
| NCT06929871 | Mako Cementless TKA vs Mako Cemented TKA | Na | Total Knee Replacement | Recruiting | 2025-09-29 | 2031-08-01 | ClinicalTrials.gov |
| NCT06929871 | Mako Cementless TKA vs Mako Cemented TKA | Na | Total Knee Replacement | Recruiting | 2025-09-29 | 2031-08-01 | ClinicalTrials.gov |
| NCT06929871 | Mako Cementless TKA vs Mako Cemented TKA | Na | Total Knee Replacement | Recruiting | 2025-09-29 | 2031-08-01 | ClinicalTrials.gov |
| NCT06570590 | Prospective Study of Minimally Invasive Lapidus Procedure for Hallux Valgus Def… | Na | Hallux Valgus and Bunion | Not_Yet_Recruiting | 2024-10-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06570590 | Prospective Study of Minimally Invasive Lapidus Procedure for Hallux Valgus Def… | Na | Hallux Valgus and Bunion | Not_Yet_Recruiting | 2024-10-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06570590 | Prospective Study of Minimally Invasive Lapidus Procedure for Hallux Valgus Def… | Na | Hallux Valgus and Bunion | Not_Yet_Recruiting | 2024-10-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06570590 | Prospective Study of Minimally Invasive Lapidus Procedure for Hallux Valgus Def… | Na | Hallux Valgus and Bunion | Not_Yet_Recruiting | 2024-10-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06570590 | Prospective Study of Minimally Invasive Lapidus Procedure for Hallux Valgus Def… | Na | Hallux Valgus and Bunion | Not_Yet_Recruiting | 2024-10-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06570590 | Prospective Study of Minimally Invasive Lapidus Procedure for Hallux Valgus Def… | Na | Hallux Valgus and Bunion | Not_Yet_Recruiting | 2024-10-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06379321 | Evaluation of Outcomes of the Triathlon Hinge Knee (THK) System | — | Knee Arthropathy | Recruiting | 2024-05-10 | 2034-05-10 | ClinicalTrials.gov |
| NCT06379321 | Evaluation of Outcomes of the Triathlon Hinge Knee (THK) System | — | Knee Arthropathy | Recruiting | 2024-05-10 | 2034-05-10 | ClinicalTrials.gov |
| NCT06379321 | Evaluation of Outcomes of the Triathlon Hinge Knee (THK) System | — | Knee Arthropathy | Recruiting | 2024-05-10 | 2034-05-10 | ClinicalTrials.gov |
| NCT06379321 | Evaluation of Outcomes of the Triathlon Hinge Knee (THK) System | — | Knee Arthropathy | Recruiting | 2024-05-10 | 2034-05-10 | ClinicalTrials.gov |
| NCT06379321 | Evaluation of Outcomes of the Triathlon Hinge Knee (THK) System | — | Knee Arthropathy | Recruiting | 2024-05-10 | 2034-05-10 | ClinicalTrials.gov |
| NCT06379321 | Evaluation of Outcomes of the Triathlon Hinge Knee (THK) System | — | Knee Arthropathy | Recruiting | 2024-05-10 | 2034-05-10 | ClinicalTrials.gov |
| NCT06284824 | Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems | Na | Knee Osteoarthritis | Not_Yet_Recruiting | 2024-05-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06284824 | Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems | Na | Knee Osteoarthritis | Not_Yet_Recruiting | 2024-05-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06284824 | Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems | Na | Knee Osteoarthritis | Not_Yet_Recruiting | 2024-05-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06284824 | Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems | Na | Knee Osteoarthritis | Not_Yet_Recruiting | 2024-05-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06284824 | Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems | Na | Knee Osteoarthritis | Not_Yet_Recruiting | 2024-05-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06284824 | Comparison of Two Robotic-Assisted Total Knee Arthroplasty Systems | Na | Knee Osteoarthritis | Not_Yet_Recruiting | 2024-05-01 | 2027-05-01 | ClinicalTrials.gov |
| NCT06368622 | Evolve China PMCF Study | — | Intracranial Aneurysm | Active_Not_Recruiting | 2024-04-24 | 2031-08-01 | ClinicalTrials.gov |
| NCT06368622 | Evolve China PMCF Study | — | Intracranial Aneurysm | Active_Not_Recruiting | 2024-04-24 | 2031-08-01 | ClinicalTrials.gov |
| NCT06368622 | Evolve China PMCF Study | — | Intracranial Aneurysm | Active_Not_Recruiting | 2024-04-24 | 2031-08-01 | ClinicalTrials.gov |
| NCT06368622 | Evolve China PMCF Study | — | Intracranial Aneurysm | Active_Not_Recruiting | 2024-04-24 | 2031-08-01 | ClinicalTrials.gov |
| NCT06368622 | Evolve China PMCF Study | — | Intracranial Aneurysm | Active_Not_Recruiting | 2024-04-24 | 2031-08-01 | ClinicalTrials.gov |
| NCT06368622 | Evolve China PMCF Study | — | Intracranial Aneurysm | Active_Not_Recruiting | 2024-04-24 | 2031-08-01 | ClinicalTrials.gov |
| NCT06169735 | Does Fluorescence With or Without Indocyanine Green Improve Parathyroid Identif… | Phase4 | Parathyroid Dysfunction | Recruiting | 2024-04-11 | 2026-05-01 | ClinicalTrials.gov |
| NCT06169735 | Does Fluorescence With or Without Indocyanine Green Improve Parathyroid Identif… | Phase4 | Parathyroid Dysfunction | Recruiting | 2024-04-11 | 2026-05-01 | ClinicalTrials.gov |
| NCT06169735 | Does Fluorescence With or Without Indocyanine Green Improve Parathyroid Identif… | Phase4 | Parathyroid Dysfunction | Recruiting | 2024-04-11 | 2026-05-01 | ClinicalTrials.gov |
| NCT06169735 | Does Fluorescence With or Without Indocyanine Green Improve Parathyroid Identif… | Phase4 | Parathyroid Dysfunction | Recruiting | 2024-04-11 | 2026-05-01 | ClinicalTrials.gov |
| NCT06169735 | Does Fluorescence With or Without Indocyanine Green Improve Parathyroid Identif… | Phase4 | Parathyroid Dysfunction | Recruiting | 2024-04-11 | 2026-05-01 | ClinicalTrials.gov |
| NCT06169735 | Does Fluorescence With or Without Indocyanine Green Improve Parathyroid Identif… | Phase4 | Parathyroid Dysfunction | Recruiting | 2024-04-11 | 2026-05-01 | ClinicalTrials.gov |
| NCT05983757 | Combined Thrombectomy for Distal MediUm Vessel Occlusion StroKe | Na | Ischemic Stroke | Recruiting | 2024-04-02 | 2027-11-01 | ClinicalTrials.gov |
| NCT05983757 | Combined Thrombectomy for Distal MediUm Vessel Occlusion StroKe | Na | Ischemic Stroke | Recruiting | 2024-04-02 | 2027-11-01 | ClinicalTrials.gov |
| NCT05983757 | Combined Thrombectomy for Distal MediUm Vessel Occlusion StroKe | Na | Ischemic Stroke | Recruiting | 2024-04-02 | 2027-11-01 | ClinicalTrials.gov |
| NCT05983757 | Combined Thrombectomy for Distal MediUm Vessel Occlusion StroKe | Na | Ischemic Stroke | Recruiting | 2024-04-02 | 2027-11-01 | ClinicalTrials.gov |
| NCT05983757 | Combined Thrombectomy for Distal MediUm Vessel Occlusion StroKe | Na | Ischemic Stroke | Recruiting | 2024-04-02 | 2027-11-01 | ClinicalTrials.gov |
| NCT05983757 | Combined Thrombectomy for Distal MediUm Vessel Occlusion StroKe | Na | Ischemic Stroke | Recruiting | 2024-04-02 | 2027-11-01 | ClinicalTrials.gov |
| NCT05591859 | Restoration Anatomic Acetabular Shell Revision Study | Na | Arthropathy | Withdrawn | 2024-03-02 | 2036-03-01 | ClinicalTrials.gov |
| NCT05591859 | Restoration Anatomic Acetabular Shell Revision Study | Na | Arthropathy | Withdrawn | 2024-03-02 | 2036-03-01 | ClinicalTrials.gov |
| NCT05591859 | Restoration Anatomic Acetabular Shell Revision Study | Na | Arthropathy | Withdrawn | 2024-03-02 | 2036-03-01 | ClinicalTrials.gov |
| NCT05591859 | Restoration Anatomic Acetabular Shell Revision Study | Na | Arthropathy | Withdrawn | 2024-03-02 | 2036-03-01 | ClinicalTrials.gov |
| NCT05591859 | Restoration Anatomic Acetabular Shell Revision Study | Na | Arthropathy | Withdrawn | 2024-03-02 | 2036-03-01 | ClinicalTrials.gov |
| NCT05591859 | Restoration Anatomic Acetabular Shell Revision Study | Na | Arthropathy | Withdrawn | 2024-03-02 | 2036-03-01 | ClinicalTrials.gov |
| NCT06080412 | Blueprint® Mixed Reality Pilot Study | — | Orthopedic Disorder | Completed | 2024-02-08 | 2025-05-07 | ClinicalTrials.gov |
| NCT06080412 | Blueprint® Mixed Reality Pilot Study | — | Orthopedic Disorder | Completed | 2024-02-08 | 2025-05-07 | ClinicalTrials.gov |
| NCT06080412 | Blueprint® Mixed Reality Pilot Study | — | Orthopedic Disorder | Completed | 2024-02-08 | 2025-05-07 | ClinicalTrials.gov |
| NCT06080412 | Blueprint® Mixed Reality Pilot Study | — | Orthopedic Disorder | Completed | 2024-02-08 | 2025-05-07 | ClinicalTrials.gov |
| NCT06080412 | Blueprint® Mixed Reality Pilot Study | — | Orthopedic Disorder | Completed | 2024-02-08 | 2025-05-07 | ClinicalTrials.gov |
| NCT06080412 | Blueprint® Mixed Reality Pilot Study | — | Orthopedic Disorder | Completed | 2024-02-08 | 2025-05-07 | ClinicalTrials.gov |
| NCT05868148 | Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study | — | Rotator Cuff Tears | Active_Not_Recruiting | 2023-10-20 | 2035-12-01 | ClinicalTrials.gov |
| NCT05868148 | Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study | — | Rotator Cuff Tears | Active_Not_Recruiting | 2023-10-20 | 2035-12-01 | ClinicalTrials.gov |
| NCT05868148 | Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study | — | Rotator Cuff Tears | Active_Not_Recruiting | 2023-10-20 | 2035-12-01 | ClinicalTrials.gov |
| NCT05868148 | Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study | — | Rotator Cuff Tears | Active_Not_Recruiting | 2023-10-20 | 2035-12-01 | ClinicalTrials.gov |
| NCT05868148 | Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study | — | Rotator Cuff Tears | Active_Not_Recruiting | 2023-10-20 | 2035-12-01 | ClinicalTrials.gov |
| NCT05868148 | Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study | — | Rotator Cuff Tears | Active_Not_Recruiting | 2023-10-20 | 2035-12-01 | ClinicalTrials.gov |
| NCT06829667 | Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients S… | — | Lateral Ankle Instability | Completed | 2023-10-13 | 2026-04-08 | ClinicalTrials.gov |
| NCT06829667 | Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients S… | — | Lateral Ankle Instability | Completed | 2023-10-13 | 2026-04-08 | ClinicalTrials.gov |
| NCT06829667 | Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients S… | — | Lateral Ankle Instability | Completed | 2023-10-13 | 2026-04-08 | ClinicalTrials.gov |
| NCT06829667 | Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients S… | — | Lateral Ankle Instability | Completed | 2023-10-13 | 2026-04-08 | ClinicalTrials.gov |
| NCT06829667 | Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients S… | — | Lateral Ankle Instability | Completed | 2023-10-13 | 2026-04-08 | ClinicalTrials.gov |
| NCT06829667 | Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients S… | — | Lateral Ankle Instability | Completed | 2023-10-13 | 2026-04-08 | ClinicalTrials.gov |
| NCT05773352 | Perform® Humeral System - Fracture Study (PFX) | — | Traumatic Arthropathy of Shoulder | Active_Not_Recruiting | 2023-08-31 | 2034-09-01 | ClinicalTrials.gov |
| NCT05773352 | Perform® Humeral System - Fracture Study (PFX) | — | Traumatic Arthropathy of Shoulder | Active_Not_Recruiting | 2023-08-31 | 2034-09-01 | ClinicalTrials.gov |
| NCT05773352 | Perform® Humeral System - Fracture Study (PFX) | — | Traumatic Arthropathy of Shoulder | Active_Not_Recruiting | 2023-08-31 | 2034-09-01 | ClinicalTrials.gov |
| NCT05773352 | Perform® Humeral System - Fracture Study (PFX) | — | Traumatic Arthropathy of Shoulder | Active_Not_Recruiting | 2023-08-31 | 2034-09-01 | ClinicalTrials.gov |
| NCT05773352 | Perform® Humeral System - Fracture Study (PFX) | — | Traumatic Arthropathy of Shoulder | Active_Not_Recruiting | 2023-08-31 | 2034-09-01 | ClinicalTrials.gov |
| NCT05773352 | Perform® Humeral System - Fracture Study (PFX) | — | Traumatic Arthropathy of Shoulder | Active_Not_Recruiting | 2023-08-31 | 2034-09-01 | ClinicalTrials.gov |
| NCT06638138 | Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction o… | Na | Lateral Ankle Instability | Completed | 2023-08-22 | 2025-12-03 | ClinicalTrials.gov |
| NCT06638138 | Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction o… | Na | Lateral Ankle Instability | Completed | 2023-08-22 | 2025-12-03 | ClinicalTrials.gov |
| NCT06638138 | Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction o… | Na | Lateral Ankle Instability | Completed | 2023-08-22 | 2025-12-03 | ClinicalTrials.gov |
| NCT06638138 | Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction o… | Na | Lateral Ankle Instability | Completed | 2023-08-22 | 2025-12-03 | ClinicalTrials.gov |
| NCT06638138 | Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction o… | Na | Lateral Ankle Instability | Completed | 2023-08-22 | 2025-12-03 | ClinicalTrials.gov |
| NCT06638138 | Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction o… | Na | Lateral Ankle Instability | Completed | 2023-08-22 | 2025-12-03 | ClinicalTrials.gov |
| NCT05842538 | Robotic Assisted Surgery In Total Knee Replacement | Na | Knee Osteoarthritis | Recruiting | 2023-04-01 | 2027-11-01 | ClinicalTrials.gov |
| NCT05842538 | Robotic Assisted Surgery In Total Knee Replacement | Na | Knee Osteoarthritis | Recruiting | 2023-04-01 | 2027-11-01 | ClinicalTrials.gov |
| NCT05842538 | Robotic Assisted Surgery In Total Knee Replacement | Na | Knee Osteoarthritis | Recruiting | 2023-04-01 | 2027-11-01 | ClinicalTrials.gov |
| NCT05842538 | Robotic Assisted Surgery In Total Knee Replacement | Na | Knee Osteoarthritis | Recruiting | 2023-04-01 | 2027-11-01 | ClinicalTrials.gov |
| NCT05842538 | Robotic Assisted Surgery In Total Knee Replacement | Na | Knee Osteoarthritis | Recruiting | 2023-04-01 | 2027-11-01 | ClinicalTrials.gov |
| NCT05842538 | Robotic Assisted Surgery In Total Knee Replacement | Na | Knee Osteoarthritis | Recruiting | 2023-04-01 | 2027-11-01 | ClinicalTrials.gov |
| NCT05523635 | Post Market Clinical Evaluation of Gamma 4 | — | Femoral Fracture | Completed | 2023-03-06 | 2025-10-16 | ClinicalTrials.gov |
| NCT05523635 | Post Market Clinical Evaluation of Gamma 4 | — | Femoral Fracture | Completed | 2023-03-06 | 2025-10-16 | ClinicalTrials.gov |
| NCT05523635 | Post Market Clinical Evaluation of Gamma 4 | — | Femoral Fracture | Completed | 2023-03-06 | 2025-10-16 | ClinicalTrials.gov |
| NCT05523635 | Post Market Clinical Evaluation of Gamma 4 | — | Femoral Fracture | Completed | 2023-03-06 | 2025-10-16 | ClinicalTrials.gov |
| NCT05523635 | Post Market Clinical Evaluation of Gamma 4 | — | Femoral Fracture | Completed | 2023-03-06 | 2025-10-16 | ClinicalTrials.gov |
| NCT05523635 | Post Market Clinical Evaluation of Gamma 4 | — | Femoral Fracture | Completed | 2023-03-06 | 2025-10-16 | ClinicalTrials.gov |
| NCT05613257 | Distal Targeter vs Free-hand | Na | Femur Fracture | Completed | 2022-10-31 | 2024-02-01 | ClinicalTrials.gov |
| NCT05613257 | Distal Targeter vs Free-hand | Na | Femur Fracture | Completed | 2022-10-31 | 2024-02-01 | ClinicalTrials.gov |
| NCT05613257 | Distal Targeter vs Free-hand | Na | Femur Fracture | Completed | 2022-10-31 | 2024-02-01 | ClinicalTrials.gov |
| NCT05613257 | Distal Targeter vs Free-hand | Na | Femur Fracture | Completed | 2022-10-31 | 2024-02-01 | ClinicalTrials.gov |
| NCT05613257 | Distal Targeter vs Free-hand | Na | Femur Fracture | Completed | 2022-10-31 | 2024-02-01 | ClinicalTrials.gov |
| NCT05613257 | Distal Targeter vs Free-hand | Na | Femur Fracture | Completed | 2022-10-31 | 2024-02-01 | ClinicalTrials.gov |
| NCT05544045 | China Surpass Streamline Post-Market Study | — | Aneurysm, Intracranial | Terminated | 2022-06-03 | 2023-09-30 | ClinicalTrials.gov |
| NCT05544045 | China Surpass Streamline Post-Market Study | — | Aneurysm, Intracranial | Terminated | 2022-06-03 | 2023-09-30 | ClinicalTrials.gov |
| NCT05544045 | China Surpass Streamline Post-Market Study | — | Aneurysm, Intracranial | Terminated | 2022-06-03 | 2023-09-30 | ClinicalTrials.gov |
| NCT05544045 | China Surpass Streamline Post-Market Study | — | Aneurysm, Intracranial | Terminated | 2022-06-03 | 2023-09-30 | ClinicalTrials.gov |
| NCT05544045 | China Surpass Streamline Post-Market Study | — | Aneurysm, Intracranial | Terminated | 2022-06-03 | 2023-09-30 | ClinicalTrials.gov |
| NCT05544045 | China Surpass Streamline Post-Market Study | — | Aneurysm, Intracranial | Terminated | 2022-06-03 | 2023-09-30 | ClinicalTrials.gov |
| NCT04692714 | Evaluation of Two Surgical Strategies for Robotic Implantation of Total Knee Pr… | Na | Total Knee Arthroplasty | Recruiting | 2022-05-16 | 2028-10-16 | ClinicalTrials.gov |
| NCT04692714 | Evaluation of Two Surgical Strategies for Robotic Implantation of Total Knee Pr… | Na | Total Knee Arthroplasty | Recruiting | 2022-05-16 | 2028-10-16 | ClinicalTrials.gov |
| NCT04692714 | Evaluation of Two Surgical Strategies for Robotic Implantation of Total Knee Pr… | Na | Total Knee Arthroplasty | Recruiting | 2022-05-16 | 2028-10-16 | ClinicalTrials.gov |
| NCT04692714 | Evaluation of Two Surgical Strategies for Robotic Implantation of Total Knee Pr… | Na | Total Knee Arthroplasty | Recruiting | 2022-05-16 | 2028-10-16 | ClinicalTrials.gov |
| NCT04692714 | Evaluation of Two Surgical Strategies for Robotic Implantation of Total Knee Pr… | Na | Total Knee Arthroplasty | Recruiting | 2022-05-16 | 2028-10-16 | ClinicalTrials.gov |
| NCT04692714 | Evaluation of Two Surgical Strategies for Robotic Implantation of Total Knee Pr… | Na | Total Knee Arthroplasty | Recruiting | 2022-05-16 | 2028-10-16 | ClinicalTrials.gov |
| NCT05144191 | Insignia™ Hip Stem Outcomes Study | Na | Hip Osteoarthritis | Active_Not_Recruiting | 2022-02-07 | 2034-04-02 | ClinicalTrials.gov |
| NCT05144191 | Insignia™ Hip Stem Outcomes Study | Na | Hip Osteoarthritis | Active_Not_Recruiting | 2022-02-07 | 2034-04-02 | ClinicalTrials.gov |
| NCT05144191 | Insignia™ Hip Stem Outcomes Study | Na | Hip Osteoarthritis | Active_Not_Recruiting | 2022-02-07 | 2034-04-02 | ClinicalTrials.gov |
| NCT05144191 | Insignia™ Hip Stem Outcomes Study | Na | Hip Osteoarthritis | Active_Not_Recruiting | 2022-02-07 | 2034-04-02 | ClinicalTrials.gov |
| NCT05144191 | Insignia™ Hip Stem Outcomes Study | Na | Hip Osteoarthritis | Active_Not_Recruiting | 2022-02-07 | 2034-04-02 | ClinicalTrials.gov |
| NCT05144191 | Insignia™ Hip Stem Outcomes Study | Na | Hip Osteoarthritis | Active_Not_Recruiting | 2022-02-07 | 2034-04-02 | 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 |
| NCT05130801 | A Study of Multiparametric MRI and pHLIP® ICG in Breast Cancer Imaging During S… | Phase1 | Breast Cancer | Recruiting | 2021-11-19 | 2027-11-01 | ClinicalTrials.gov |
| NCT05130801 | A Study of Multiparametric MRI and pHLIP® ICG in Breast Cancer Imaging During S… | Phase1 | Breast Cancer | Recruiting | 2021-11-19 | 2027-11-01 | ClinicalTrials.gov |
| NCT05130801 | A Study of Multiparametric MRI and pHLIP® ICG in Breast Cancer Imaging During S… | Phase1 | Breast Cancer | Recruiting | 2021-11-19 | 2027-11-01 | ClinicalTrials.gov |
| NCT05130801 | A Study of Multiparametric MRI and pHLIP® ICG in Breast Cancer Imaging During S… | Phase1 | Breast Cancer | Recruiting | 2021-11-19 | 2027-11-01 | ClinicalTrials.gov |
| NCT05130801 | A Study of Multiparametric MRI and pHLIP® ICG in Breast Cancer Imaging During S… | Phase1 | Breast Cancer | Recruiting | 2021-11-19 | 2027-11-01 | ClinicalTrials.gov |
| NCT05130801 | A Study of Multiparametric MRI and pHLIP® ICG in Breast Cancer Imaging During S… | Phase1 | Breast Cancer | Recruiting | 2021-11-19 | 2027-11-01 | ClinicalTrials.gov |
| NCT05049993 | Pyrocarbon Clinical Follow-up Study | — | Osteoarthritis of the Shoulder | Active_Not_Recruiting | 2021-10-27 | 2027-12-31 | ClinicalTrials.gov |
| NCT05049993 | Pyrocarbon Clinical Follow-up Study | — | Osteoarthritis of the Shoulder | Active_Not_Recruiting | 2021-10-27 | 2027-12-31 | ClinicalTrials.gov |
| NCT05049993 | Pyrocarbon Clinical Follow-up Study | — | Osteoarthritis of the Shoulder | Active_Not_Recruiting | 2021-10-27 | 2027-12-31 | ClinicalTrials.gov |
| NCT05049993 | Pyrocarbon Clinical Follow-up Study | — | Osteoarthritis of the Shoulder | Active_Not_Recruiting | 2021-10-27 | 2027-12-31 | ClinicalTrials.gov |
| NCT05049993 | Pyrocarbon Clinical Follow-up Study | — | Osteoarthritis of the Shoulder | Active_Not_Recruiting | 2021-10-27 | 2027-12-31 | ClinicalTrials.gov |
| NCT05049993 | Pyrocarbon Clinical Follow-up Study | — | Osteoarthritis of the Shoulder | Active_Not_Recruiting | 2021-10-27 | 2027-12-31 | ClinicalTrials.gov |
| NCT05744895 | MAKO Total Knee Artroplasty | — | Osteoarthritis, Knee | Completed | 2021-09-14 | 2025-06-30 | ClinicalTrials.gov |
| NCT05744895 | MAKO Total Knee Artroplasty | — | Osteoarthritis, Knee | Completed | 2021-09-14 | 2025-06-30 | ClinicalTrials.gov |
| NCT05744895 | MAKO Total Knee Artroplasty | — | Osteoarthritis, Knee | Completed | 2021-09-14 | 2025-06-30 | ClinicalTrials.gov |
| NCT05744895 | MAKO Total Knee Artroplasty | — | Osteoarthritis, Knee | Completed | 2021-09-14 | 2025-06-30 | ClinicalTrials.gov |
| NCT05744895 | MAKO Total Knee Artroplasty | — | Osteoarthritis, Knee | Completed | 2021-09-14 | 2025-06-30 | ClinicalTrials.gov |
| NCT05744895 | MAKO Total Knee Artroplasty | — | Osteoarthritis, Knee | Completed | 2021-09-14 | 2025-06-30 | ClinicalTrials.gov |
| NCT05067543 | Perform Humeral System Study | — | Osteoarthritis Shoulder | Recruiting | 2021-09-12 | 2036-12-01 | ClinicalTrials.gov |
| NCT05067543 | Perform Humeral System Study | — | Osteoarthritis Shoulder | Recruiting | 2021-09-12 | 2036-12-01 | ClinicalTrials.gov |
| NCT05067543 | Perform Humeral System Study | — | Osteoarthritis Shoulder | Recruiting | 2021-09-12 | 2036-12-01 | ClinicalTrials.gov |
| NCT05067543 | Perform Humeral System Study | — | Osteoarthritis Shoulder | Recruiting | 2021-09-12 | 2036-12-01 | ClinicalTrials.gov |
| NCT05067543 | Perform Humeral System Study | — | Osteoarthritis Shoulder | Recruiting | 2021-09-12 | 2036-12-01 | ClinicalTrials.gov |
| NCT05067543 | Perform Humeral System Study | — | Osteoarthritis Shoulder | Recruiting | 2021-09-12 | 2036-12-01 | ClinicalTrials.gov |
| NCT04561414 | Objective to Evaluate the Safety and Effectiveness of LED Light Source System f… | Na | Lower Abdominal Surgery | Withdrawn | 2021-05-01 | 2022-05-01 | ClinicalTrials.gov |
| NCT04561414 | Objective to Evaluate the Safety and Effectiveness of LED Light Source System f… | Na | Lower Abdominal Surgery | Withdrawn | 2021-05-01 | 2022-05-01 | ClinicalTrials.gov |
| NCT04561414 | Objective to Evaluate the Safety and Effectiveness of LED Light Source System f… | Na | Lower Abdominal Surgery | Withdrawn | 2021-05-01 | 2022-05-01 | ClinicalTrials.gov |
| NCT04561414 | Objective to Evaluate the Safety and Effectiveness of LED Light Source System f… | Na | Lower Abdominal Surgery | Withdrawn | 2021-05-01 | 2022-05-01 | ClinicalTrials.gov |
| NCT04561414 | Objective to Evaluate the Safety and Effectiveness of LED Light Source System f… | Na | Lower Abdominal Surgery | Withdrawn | 2021-05-01 | 2022-05-01 | ClinicalTrials.gov |
| NCT04561414 | Objective to Evaluate the Safety and Effectiveness of LED Light Source System f… | Na | Lower Abdominal Surgery | Withdrawn | 2021-05-01 | 2022-05-01 | ClinicalTrials.gov |
| NCT04719156 | Fluorescent Intra-operative Tumor Margin Examination | Phase2 | Sarcoma | Recruiting | 2021-03-02 | 2026-12-31 | ClinicalTrials.gov |
| NCT04719156 | Fluorescent Intra-operative Tumor Margin Examination | Phase2 | Sarcoma | Recruiting | 2021-03-02 | 2026-12-31 | ClinicalTrials.gov |
| NCT04719156 | Fluorescent Intra-operative Tumor Margin Examination | Phase2 | Sarcoma | Recruiting | 2021-03-02 | 2026-12-31 | ClinicalTrials.gov |
| NCT04719156 | Fluorescent Intra-operative Tumor Margin Examination | Phase2 | Sarcoma | Recruiting | 2021-03-02 | 2026-12-31 | ClinicalTrials.gov |
| NCT04719156 | Fluorescent Intra-operative Tumor Margin Examination | Phase2 | Sarcoma | Recruiting | 2021-03-02 | 2026-12-31 | ClinicalTrials.gov |
| NCT04719156 | Fluorescent Intra-operative Tumor Margin Examination | Phase2 | Sarcoma | Recruiting | 2021-03-02 | 2026-12-31 | ClinicalTrials.gov |
| NCT04594993 | INFINITY™ With ADAPTIS™ Technology Study | — | Arthritis, Rheumatoid | Active_Not_Recruiting | 2021-02-09 | 2035-11-01 | ClinicalTrials.gov |
| NCT04594993 | INFINITY™ With ADAPTIS™ Technology Study | — | Arthritis, Rheumatoid | Active_Not_Recruiting | 2021-02-09 | 2035-11-01 | ClinicalTrials.gov |
| NCT04594993 | INFINITY™ With ADAPTIS™ Technology Study | — | Arthritis, Rheumatoid | Active_Not_Recruiting | 2021-02-09 | 2035-11-01 | ClinicalTrials.gov |
| NCT04594993 | INFINITY™ With ADAPTIS™ Technology Study | — | Arthritis, Rheumatoid | Active_Not_Recruiting | 2021-02-09 | 2035-11-01 | ClinicalTrials.gov |
| NCT04594993 | INFINITY™ With ADAPTIS™ Technology Study | — | Arthritis, Rheumatoid | Active_Not_Recruiting | 2021-02-09 | 2035-11-01 | ClinicalTrials.gov |
| NCT04594993 | INFINITY™ With ADAPTIS™ Technology Study | — | Arthritis, Rheumatoid | Active_Not_Recruiting | 2021-02-09 | 2035-11-01 | ClinicalTrials.gov |
| NCT04618770 | Triathlon PSR Outcomes Study | Na | Arthroplasty | Terminated | 2021-02-08 | 2023-01-27 | ClinicalTrials.gov |
| NCT04618770 | Triathlon PSR Outcomes Study | Na | Arthroplasty | Terminated | 2021-02-08 | 2023-01-27 | ClinicalTrials.gov |
| NCT04618770 | Triathlon PSR Outcomes Study | Na | Arthroplasty | Terminated | 2021-02-08 | 2023-01-27 | ClinicalTrials.gov |
| NCT04618770 | Triathlon PSR Outcomes Study | Na | Arthroplasty | Terminated | 2021-02-08 | 2023-01-27 | ClinicalTrials.gov |
| NCT04618770 | Triathlon PSR Outcomes Study | Na | Arthroplasty | Terminated | 2021-02-08 | 2023-01-27 | ClinicalTrials.gov |
| NCT04618770 | Triathlon PSR Outcomes Study | Na | Arthroplasty | Terminated | 2021-02-08 | 2023-01-27 | ClinicalTrials.gov |
| NCT04646096 | Multicenter Study for Robotic Arm-assisted THA 4.0 System: Hip Spine Relationsh… | Na | Osteoarthritis, Hip | Completed | 2021-01-01 | 2024-10-10 | ClinicalTrials.gov |
| NCT04646096 | Multicenter Study for Robotic Arm-assisted THA 4.0 System: Hip Spine Relationsh… | Na | Osteoarthritis, Hip | Completed | 2021-01-01 | 2024-10-10 | ClinicalTrials.gov |
| NCT04646096 | Multicenter Study for Robotic Arm-assisted THA 4.0 System: Hip Spine Relationsh… | Na | Osteoarthritis, Hip | Completed | 2021-01-01 | 2024-10-10 | ClinicalTrials.gov |
| NCT04646096 | Multicenter Study for Robotic Arm-assisted THA 4.0 System: Hip Spine Relationsh… | Na | Osteoarthritis, Hip | Completed | 2021-01-01 | 2024-10-10 | ClinicalTrials.gov |
| NCT04646096 | Multicenter Study for Robotic Arm-assisted THA 4.0 System: Hip Spine Relationsh… | Na | Osteoarthritis, Hip | Completed | 2021-01-01 | 2024-10-10 | ClinicalTrials.gov |
| NCT04646096 | Multicenter Study for Robotic Arm-assisted THA 4.0 System: Hip Spine Relationsh… | Na | Osteoarthritis, Hip | Completed | 2021-01-01 | 2024-10-10 | ClinicalTrials.gov |
| NCT04380350 | Trenza Embolization Device for Intrasaccular Aneurysm Treatment | — | Aneurysm | Completed | 2020-12-17 | 2026-02-12 | ClinicalTrials.gov |
| NCT04380350 | Trenza Embolization Device for Intrasaccular Aneurysm Treatment | — | Aneurysm | Completed | 2020-12-17 | 2026-02-12 | ClinicalTrials.gov |
| NCT04380350 | Trenza Embolization Device for Intrasaccular Aneurysm Treatment | — | Aneurysm | Completed | 2020-12-17 | 2026-02-12 | ClinicalTrials.gov |
| NCT04380350 | Trenza Embolization Device for Intrasaccular Aneurysm Treatment | — | Aneurysm | Completed | 2020-12-17 | 2026-02-12 | ClinicalTrials.gov |
| NCT04380350 | Trenza Embolization Device for Intrasaccular Aneurysm Treatment | — | Aneurysm | Completed | 2020-12-17 | 2026-02-12 | ClinicalTrials.gov |
| NCT04380350 | Trenza Embolization Device for Intrasaccular Aneurysm Treatment | — | Aneurysm | Completed | 2020-12-17 | 2026-02-12 | ClinicalTrials.gov |
| NCT04585568 | Validation of Ballistocardiographic Biosensors and Other Hemodynamic Measures f… | — | Hemodynamics | Completed | 2020-09-28 | 2020-09-30 | ClinicalTrials.gov |
| NCT04585568 | Validation of Ballistocardiographic Biosensors and Other Hemodynamic Measures f… | — | Hemodynamics | Completed | 2020-09-28 | 2020-09-30 | ClinicalTrials.gov |
| NCT04585568 | Validation of Ballistocardiographic Biosensors and Other Hemodynamic Measures f… | — | Hemodynamics | Completed | 2020-09-28 | 2020-09-30 | ClinicalTrials.gov |
| NCT04585568 | Validation of Ballistocardiographic Biosensors and Other Hemodynamic Measures f… | — | Hemodynamics | Completed | 2020-09-28 | 2020-09-30 | ClinicalTrials.gov |
| NCT04585568 | Validation of Ballistocardiographic Biosensors and Other Hemodynamic Measures f… | — | Hemodynamics | Completed | 2020-09-28 | 2020-09-30 | ClinicalTrials.gov |
| NCT04585568 | Validation of Ballistocardiographic Biosensors and Other Hemodynamic Measures f… | — | Hemodynamics | Completed | 2020-09-28 | 2020-09-30 | ClinicalTrials.gov |
| NCT04561583 | Effectiveness and Safety of LED Light Source System for Endoscope | Na | Laparoscopic Cholecystectomy | Withdrawn | 2020-09-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT04379921 | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using t… | Na | Spine Disease | Completed | 2020-09-01 | 2024-11-30 | ClinicalTrials.gov |
| NCT04561583 | Effectiveness and Safety of LED Light Source System for Endoscope | Na | Laparoscopic Cholecystectomy | Withdrawn | 2020-09-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT04379921 | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using t… | Na | Spine Disease | Completed | 2020-09-01 | 2024-11-30 | ClinicalTrials.gov |
| NCT04379921 | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using t… | Na | Spine Disease | Completed | 2020-09-01 | 2024-11-30 | ClinicalTrials.gov |
| NCT04379921 | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using t… | Na | Spine Disease | Completed | 2020-09-01 | 2024-11-30 | ClinicalTrials.gov |
| NCT04561583 | Effectiveness and Safety of LED Light Source System for Endoscope | Na | Laparoscopic Cholecystectomy | Withdrawn | 2020-09-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT04561583 | Effectiveness and Safety of LED Light Source System for Endoscope | Na | Laparoscopic Cholecystectomy | Withdrawn | 2020-09-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT04561583 | Effectiveness and Safety of LED Light Source System for Endoscope | Na | Laparoscopic Cholecystectomy | Withdrawn | 2020-09-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT04379921 | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using t… | Na | Spine Disease | Completed | 2020-09-01 | 2024-11-30 | ClinicalTrials.gov |
| NCT04379921 | Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using t… | Na | Spine Disease | Completed | 2020-09-01 | 2024-11-30 | ClinicalTrials.gov |
| NCT04561583 | Effectiveness and Safety of LED Light Source System for Endoscope | Na | Laparoscopic Cholecystectomy | Withdrawn | 2020-09-01 | 2021-09-01 | ClinicalTrials.gov |
| NCT04350255 | A Register Based Prospective Study During Implementation of a New Cup | Na | Prospective | Recruiting | 2020-08-01 | 2030-08-01 | ClinicalTrials.gov |
| NCT04350255 | A Register Based Prospective Study During Implementation of a New Cup | Na | Prospective | Recruiting | 2020-08-01 | 2030-08-01 | ClinicalTrials.gov |
| NCT04350255 | A Register Based Prospective Study During Implementation of a New Cup | Na | Prospective | Recruiting | 2020-08-01 | 2030-08-01 | ClinicalTrials.gov |
| NCT04350255 | A Register Based Prospective Study During Implementation of a New Cup | Na | Prospective | Recruiting | 2020-08-01 | 2030-08-01 | ClinicalTrials.gov |
| NCT04350255 | A Register Based Prospective Study During Implementation of a New Cup | Na | Prospective | Recruiting | 2020-08-01 | 2030-08-01 | ClinicalTrials.gov |
| NCT04350255 | A Register Based Prospective Study During Implementation of a New Cup | Na | Prospective | Recruiting | 2020-08-01 | 2030-08-01 | ClinicalTrials.gov |
| NCT04195568 | Evaluation of Safety and Effectiveness of Stryker Surpass Evolve™ Flow Diverter… | Na | Aneurysm, Intracranial | Active_Not_Recruiting | 2020-07-07 | 2028-09-13 | ClinicalTrials.gov |
| NCT04195568 | Evaluation of Safety and Effectiveness of Stryker Surpass Evolve™ Flow Diverter… | Na | Aneurysm, Intracranial | Active_Not_Recruiting | 2020-07-07 | 2028-09-13 | ClinicalTrials.gov |
| NCT04195568 | Evaluation of Safety and Effectiveness of Stryker Surpass Evolve™ Flow Diverter… | Na | Aneurysm, Intracranial | Active_Not_Recruiting | 2020-07-07 | 2028-09-13 | ClinicalTrials.gov |
| NCT04195568 | Evaluation of Safety and Effectiveness of Stryker Surpass Evolve™ Flow Diverter… | Na | Aneurysm, Intracranial | Active_Not_Recruiting | 2020-07-07 | 2028-09-13 | ClinicalTrials.gov |
| NCT04195568 | Evaluation of Safety and Effectiveness of Stryker Surpass Evolve™ Flow Diverter… | Na | Aneurysm, Intracranial | Active_Not_Recruiting | 2020-07-07 | 2028-09-13 | ClinicalTrials.gov |
| NCT04195568 | Evaluation of Safety and Effectiveness of Stryker Surpass Evolve™ Flow Diverter… | Na | Aneurysm, Intracranial | Active_Not_Recruiting | 2020-07-07 | 2028-09-13 | ClinicalTrials.gov |
| NCT04317586 | Trident II Revision Outcomes Study | Na | Arthroplasty, Hip Revision | Terminated | 2020-06-23 | 2023-01-27 | ClinicalTrials.gov |
| NCT04317586 | Trident II Revision Outcomes Study | Na | Arthroplasty, Hip Revision | Terminated | 2020-06-23 | 2023-01-27 | ClinicalTrials.gov |
| NCT04317586 | Trident II Revision Outcomes Study | Na | Arthroplasty, Hip Revision | Terminated | 2020-06-23 | 2023-01-27 | ClinicalTrials.gov |
| NCT04317586 | Trident II Revision Outcomes Study | Na | Arthroplasty, Hip Revision | Terminated | 2020-06-23 | 2023-01-27 | ClinicalTrials.gov |
| NCT04317586 | Trident II Revision Outcomes Study | Na | Arthroplasty, Hip Revision | Terminated | 2020-06-23 | 2023-01-27 | ClinicalTrials.gov |
| NCT04317586 | Trident II Revision Outcomes Study | Na | Arthroplasty, Hip Revision | Terminated | 2020-06-23 | 2023-01-27 | ClinicalTrials.gov |
| NCT04173377 | Elbow Outcomes Clinical Study (WELBOW) | — | Orthopedic Disorder | Completed | 2020-06-08 | 2024-09-17 | ClinicalTrials.gov |
| NCT04173377 | Elbow Outcomes Clinical Study (WELBOW) | — | Orthopedic Disorder | Completed | 2020-06-08 | 2024-09-17 | ClinicalTrials.gov |
| NCT04173377 | Elbow Outcomes Clinical Study (WELBOW) | — | Orthopedic Disorder | Completed | 2020-06-08 | 2024-09-17 | ClinicalTrials.gov |
| NCT04173377 | Elbow Outcomes Clinical Study (WELBOW) | — | Orthopedic Disorder | Completed | 2020-06-08 | 2024-09-17 | ClinicalTrials.gov |
| NCT04173377 | Elbow Outcomes Clinical Study (WELBOW) | — | Orthopedic Disorder | Completed | 2020-06-08 | 2024-09-17 | ClinicalTrials.gov |
| NCT04173377 | Elbow Outcomes Clinical Study (WELBOW) | — | Orthopedic Disorder | Completed | 2020-06-08 | 2024-09-17 | ClinicalTrials.gov |
| NCT04474665 | Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arth… | Na | Reverse Shoulder Replacement | Unknown | 2020-03-16 | 2021-06-01 | ClinicalTrials.gov |
| NCT04474665 | Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arth… | Na | Reverse Shoulder Replacement | Unknown | 2020-03-16 | 2021-06-01 | ClinicalTrials.gov |
| NCT04474665 | Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arth… | Na | Reverse Shoulder Replacement | Unknown | 2020-03-16 | 2021-06-01 | ClinicalTrials.gov |
| NCT04474665 | Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arth… | Na | Reverse Shoulder Replacement | Unknown | 2020-03-16 | 2021-06-01 | ClinicalTrials.gov |
| NCT04474665 | Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arth… | Na | Reverse Shoulder Replacement | Unknown | 2020-03-16 | 2021-06-01 | ClinicalTrials.gov |
| NCT04474665 | Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arth… | Na | Reverse Shoulder Replacement | Unknown | 2020-03-16 | 2021-06-01 | ClinicalTrials.gov |
| NCT04265222 | Cam Decompression Utilizing the Stryker Hip-Check Software Platform | Na | Femoroacetabular Impingement | Active_Not_Recruiting | 2020-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04265222 | Cam Decompression Utilizing the Stryker Hip-Check Software Platform | Na | Femoroacetabular Impingement | Active_Not_Recruiting | 2020-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04265222 | Cam Decompression Utilizing the Stryker Hip-Check Software Platform | Na | Femoroacetabular Impingement | Active_Not_Recruiting | 2020-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04265222 | Cam Decompression Utilizing the Stryker Hip-Check Software Platform | Na | Femoroacetabular Impingement | Active_Not_Recruiting | 2020-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04265222 | Cam Decompression Utilizing the Stryker Hip-Check Software Platform | Na | Femoroacetabular Impingement | Active_Not_Recruiting | 2020-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04265222 | Cam Decompression Utilizing the Stryker Hip-Check Software Platform | Na | Femoroacetabular Impingement | Active_Not_Recruiting | 2020-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT04118894 | Wright Foot & Ankle Post-Market Observational Study | — | Arthritis | Terminated | 2020-01-22 | 2023-07-12 | ClinicalTrials.gov |
| NCT04118894 | Wright Foot & Ankle Post-Market Observational Study | — | Arthritis | Terminated | 2020-01-22 | 2023-07-12 | ClinicalTrials.gov |
| NCT04118894 | Wright Foot & Ankle Post-Market Observational Study | — | Arthritis | Terminated | 2020-01-22 | 2023-07-12 | ClinicalTrials.gov |
| NCT04118894 | Wright Foot & Ankle Post-Market Observational Study | — | Arthritis | Terminated | 2020-01-22 | 2023-07-12 | ClinicalTrials.gov |
| NCT04118894 | Wright Foot & Ankle Post-Market Observational Study | — | Arthritis | Terminated | 2020-01-22 | 2023-07-12 | ClinicalTrials.gov |
| NCT04118894 | Wright Foot & Ankle Post-Market Observational Study | — | Arthritis | Terminated | 2020-01-22 | 2023-07-12 | ClinicalTrials.gov |
| NCT02452957 | Safety and Effectiveness of the Tornier Simpliciti™ Shoulder System in Shoulder… | — | Shoulder Osteoarthritis | Withdrawn | 2020-01-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02452957 | Safety and Effectiveness of the Tornier Simpliciti™ Shoulder System in Shoulder… | — | Shoulder Osteoarthritis | Withdrawn | 2020-01-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02452957 | Safety and Effectiveness of the Tornier Simpliciti™ Shoulder System in Shoulder… | — | Shoulder Osteoarthritis | Withdrawn | 2020-01-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02452957 | Safety and Effectiveness of the Tornier Simpliciti™ Shoulder System in Shoulder… | — | Shoulder Osteoarthritis | Withdrawn | 2020-01-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02452957 | Safety and Effectiveness of the Tornier Simpliciti™ Shoulder System in Shoulder… | — | Shoulder Osteoarthritis | Withdrawn | 2020-01-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT02452957 | Safety and Effectiveness of the Tornier Simpliciti™ Shoulder System in Shoulder… | — | Shoulder Osteoarthritis | Withdrawn | 2020-01-01 | 2022-01-01 | ClinicalTrials.gov |
| NCT04162483 | Safety and Performance of the Neuroform Atlas™ Stent System | — | Intracranial Aneurysm | Unknown | 2019-11-19 | 2021-07-15 | ClinicalTrials.gov |
| NCT04162483 | Safety and Performance of the Neuroform Atlas™ Stent System | — | Intracranial Aneurysm | Unknown | 2019-11-19 | 2021-07-15 | ClinicalTrials.gov |
| NCT04162483 | Safety and Performance of the Neuroform Atlas™ Stent System | — | Intracranial Aneurysm | Unknown | 2019-11-19 | 2021-07-15 | ClinicalTrials.gov |
| NCT04162483 | Safety and Performance of the Neuroform Atlas™ Stent System | — | Intracranial Aneurysm | Unknown | 2019-11-19 | 2021-07-15 | ClinicalTrials.gov |
| NCT04162483 | Safety and Performance of the Neuroform Atlas™ Stent System | — | Intracranial Aneurysm | Unknown | 2019-11-19 | 2021-07-15 | ClinicalTrials.gov |
| NCT04162483 | Safety and Performance of the Neuroform Atlas™ Stent System | — | Intracranial Aneurysm | Unknown | 2019-11-19 | 2021-07-15 | ClinicalTrials.gov |
| NCT04137237 | Hand & Wrist Pyrocarbon Implants Outcomes Clinical Study | — | Orthopedics | Recruiting | 2019-11-14 | 2033-01-01 | ClinicalTrials.gov |
| NCT04137237 | Hand & Wrist Pyrocarbon Implants Outcomes Clinical Study | — | Orthopedics | Recruiting | 2019-11-14 | 2033-01-01 | ClinicalTrials.gov |
| NCT04137237 | Hand & Wrist Pyrocarbon Implants Outcomes Clinical Study | — | Orthopedics | Recruiting | 2019-11-14 | 2033-01-01 | ClinicalTrials.gov |
| NCT04137237 | Hand & Wrist Pyrocarbon Implants Outcomes Clinical Study | — | Orthopedics | Recruiting | 2019-11-14 | 2033-01-01 | ClinicalTrials.gov |
| NCT04137237 | Hand & Wrist Pyrocarbon Implants Outcomes Clinical Study | — | Orthopedics | Recruiting | 2019-11-14 | 2033-01-01 | ClinicalTrials.gov |
| NCT04137237 | Hand & Wrist Pyrocarbon Implants Outcomes Clinical Study | — | Orthopedics | Recruiting | 2019-11-14 | 2033-01-01 | ClinicalTrials.gov |
| NCT04089371 | A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) Syst… | — | Arthroplasty | Terminated | 2019-10-01 | 2022-07-08 | ClinicalTrials.gov |
| NCT04089371 | A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) Syst… | — | Arthroplasty | Terminated | 2019-10-01 | 2022-07-08 | ClinicalTrials.gov |
| NCT04089371 | A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) Syst… | — | Arthroplasty | Terminated | 2019-10-01 | 2022-07-08 | ClinicalTrials.gov |
| NCT04089371 | A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) Syst… | — | Arthroplasty | Terminated | 2019-10-01 | 2022-07-08 | ClinicalTrials.gov |
| NCT04089371 | A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) Syst… | — | Arthroplasty | Terminated | 2019-10-01 | 2022-07-08 | ClinicalTrials.gov |
| NCT04089371 | A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) Syst… | — | Arthroplasty | Terminated | 2019-10-01 | 2022-07-08 | ClinicalTrials.gov |
| NCT03700125 | Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac… | Na | Death, Sudden, Cardiac | Completed | 2019-09-23 | 2022-12-15 | ClinicalTrials.gov |
| NCT03700125 | Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac… | Na | Death, Sudden, Cardiac | Completed | 2019-09-23 | 2022-12-15 | ClinicalTrials.gov |
| NCT03700125 | Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac… | Na | Death, Sudden, Cardiac | Completed | 2019-09-23 | 2022-12-15 | ClinicalTrials.gov |
| NCT03700125 | Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac… | Na | Death, Sudden, Cardiac | Completed | 2019-09-23 | 2022-12-15 | ClinicalTrials.gov |
| NCT03700125 | Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac… | Na | Death, Sudden, Cardiac | Completed | 2019-09-23 | 2022-12-15 | ClinicalTrials.gov |
| NCT03700125 | Pre-hospital ECMO in Advanced Resuscitation in Patients With Refractory Cardiac… | Na | Death, Sudden, Cardiac | Completed | 2019-09-23 | 2022-12-15 | ClinicalTrials.gov |
| NCT04015128 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2026-04-16 | ClinicalTrials.gov |
| NCT04015154 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2025-09-15 | ClinicalTrials.gov |
| NCT04015128 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2026-04-16 | ClinicalTrials.gov |
| NCT04015167 | A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the … | — | Tibial Fractures | Completed | 2019-09-12 | 2023-08-08 | ClinicalTrials.gov |
| NCT04015167 | A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the … | — | Tibial Fractures | Completed | 2019-09-12 | 2023-08-08 | ClinicalTrials.gov |
| NCT04015167 | A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the … | — | Tibial Fractures | Completed | 2019-09-12 | 2023-08-08 | ClinicalTrials.gov |
| NCT04015154 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2025-09-15 | ClinicalTrials.gov |
| NCT04015167 | A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the … | — | Tibial Fractures | Completed | 2019-09-12 | 2023-08-08 | ClinicalTrials.gov |
| NCT04015154 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2025-09-15 | ClinicalTrials.gov |
| NCT04015128 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2026-04-16 | ClinicalTrials.gov |
| NCT04015167 | A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the … | — | Tibial Fractures | Completed | 2019-09-12 | 2023-08-08 | ClinicalTrials.gov |
| NCT04015154 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2025-09-15 | ClinicalTrials.gov |
| NCT04015128 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2026-04-16 | ClinicalTrials.gov |
| NCT04015128 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2026-04-16 | ClinicalTrials.gov |
| NCT04015154 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2025-09-15 | ClinicalTrials.gov |
| NCT04015167 | A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the … | — | Tibial Fractures | Completed | 2019-09-12 | 2023-08-08 | ClinicalTrials.gov |
| NCT04015154 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2025-09-15 | ClinicalTrials.gov |
| NCT04015128 | A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the … | — | Femoral Fracture | Completed | 2019-09-12 | 2026-04-16 | ClinicalTrials.gov |
| NCT04019925 | Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis | Na | Arthroplasty, Replacement, Hip | Unknown | 2019-09-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT04019925 | Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis | Na | Arthroplasty, Replacement, Hip | Unknown | 2019-09-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT04019925 | Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis | Na | Arthroplasty, Replacement, Hip | Unknown | 2019-09-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT04019925 | Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis | Na | Arthroplasty, Replacement, Hip | Unknown | 2019-09-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT04019925 | Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis | Na | Arthroplasty, Replacement, Hip | Unknown | 2019-09-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT04019925 | Assessing the Wear Rates of the ADM/MDM Hips Using 3D X-ray Analysis | Na | Arthroplasty, Replacement, Hip | Unknown | 2019-09-01 | 2020-08-31 | ClinicalTrials.gov |
| NCT04795765 | SpineJack System Postmarket Registry | — | Osteoporotic Vertebral Compression Fractures | Completed | 2019-08-19 | 2024-11-11 | ClinicalTrials.gov |
| NCT04795765 | SpineJack System Postmarket Registry | — | Osteoporotic Vertebral Compression Fractures | Completed | 2019-08-19 | 2024-11-11 | ClinicalTrials.gov |
| NCT04795765 | SpineJack System Postmarket Registry | — | Osteoporotic Vertebral Compression Fractures | Completed | 2019-08-19 | 2024-11-11 | ClinicalTrials.gov |
| NCT04795765 | SpineJack System Postmarket Registry | — | Osteoporotic Vertebral Compression Fractures | Completed | 2019-08-19 | 2024-11-11 | ClinicalTrials.gov |
| NCT04795765 | SpineJack System Postmarket Registry | — | Osteoporotic Vertebral Compression Fractures | Completed | 2019-08-19 | 2024-11-11 | ClinicalTrials.gov |
| NCT04795765 | SpineJack System Postmarket Registry | — | Osteoporotic Vertebral Compression Fractures | Completed | 2019-08-19 | 2024-11-11 | ClinicalTrials.gov |
| NCT04057352 | Citadel Embolization Device Study | Na | Unruptured Wide-neck Aneurysms | Active_Not_Recruiting | 2019-07-18 | 2026-11-15 | ClinicalTrials.gov |
| NCT04057352 | Citadel Embolization Device Study | Na | Unruptured Wide-neck Aneurysms | Active_Not_Recruiting | 2019-07-18 | 2026-11-15 | ClinicalTrials.gov |
| NCT04057352 | Citadel Embolization Device Study | Na | Unruptured Wide-neck Aneurysms | Active_Not_Recruiting | 2019-07-18 | 2026-11-15 | ClinicalTrials.gov |
| NCT04057352 | Citadel Embolization Device Study | Na | Unruptured Wide-neck Aneurysms | Active_Not_Recruiting | 2019-07-18 | 2026-11-15 | ClinicalTrials.gov |
| NCT04057352 | Citadel Embolization Device Study | Na | Unruptured Wide-neck Aneurysms | Active_Not_Recruiting | 2019-07-18 | 2026-11-15 | ClinicalTrials.gov |
| NCT04057352 | Citadel Embolization Device Study | Na | Unruptured Wide-neck Aneurysms | Active_Not_Recruiting | 2019-07-18 | 2026-11-15 | ClinicalTrials.gov |
| NCT03846791 | An Evaluation of Health Outcomes for Mako Hip Replacement | — | Osteoarthritis, Hip | Completed | 2019-07-15 | 2024-05-03 | ClinicalTrials.gov |
| NCT03846791 | An Evaluation of Health Outcomes for Mako Hip Replacement | — | Osteoarthritis, Hip | Completed | 2019-07-15 | 2024-05-03 | ClinicalTrials.gov |
| NCT03846791 | An Evaluation of Health Outcomes for Mako Hip Replacement | — | Osteoarthritis, Hip | Completed | 2019-07-15 | 2024-05-03 | ClinicalTrials.gov |
| NCT03846791 | An Evaluation of Health Outcomes for Mako Hip Replacement | — | Osteoarthritis, Hip | Completed | 2019-07-15 | 2024-05-03 | ClinicalTrials.gov |
| NCT03846791 | An Evaluation of Health Outcomes for Mako Hip Replacement | — | Osteoarthritis, Hip | Completed | 2019-07-15 | 2024-05-03 | ClinicalTrials.gov |
| NCT03846791 | An Evaluation of Health Outcomes for Mako Hip Replacement | — | Osteoarthritis, Hip | Completed | 2019-07-15 | 2024-05-03 | ClinicalTrials.gov |
| NCT03880955 | A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty … | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2023-12-13 | ClinicalTrials.gov |
| NCT03858517 | A Post-Market Clinical Evaluation of the ReUnion TSA System | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2022-07-08 | ClinicalTrials.gov |
| NCT03858517 | A Post-Market Clinical Evaluation of the ReUnion TSA System | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2022-07-08 | ClinicalTrials.gov |
| NCT03880955 | A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty … | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2023-12-13 | ClinicalTrials.gov |
| NCT03858517 | A Post-Market Clinical Evaluation of the ReUnion TSA System | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2022-07-08 | ClinicalTrials.gov |
| NCT03880955 | A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty … | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2023-12-13 | ClinicalTrials.gov |
| NCT03880955 | A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty … | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2023-12-13 | ClinicalTrials.gov |
| NCT03880955 | A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty … | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2023-12-13 | ClinicalTrials.gov |
| NCT03858517 | A Post-Market Clinical Evaluation of the ReUnion TSA System | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2022-07-08 | ClinicalTrials.gov |
| NCT03880955 | A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty … | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2023-12-13 | ClinicalTrials.gov |
| NCT03858517 | A Post-Market Clinical Evaluation of the ReUnion TSA System | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2022-07-08 | ClinicalTrials.gov |
| NCT03858517 | A Post-Market Clinical Evaluation of the ReUnion TSA System | — | Shoulder Arthroplasty | Terminated | 2019-06-25 | 2022-07-08 | ClinicalTrials.gov |
| NCT03891199 | Two Year Study With Robotic-Arm Assisted Hip Surgery. | Na | Surgery | Completed | 2019-04-08 | 2020-08-01 | ClinicalTrials.gov |
| NCT03891199 | Two Year Study With Robotic-Arm Assisted Hip Surgery. | Na | Surgery | Completed | 2019-04-08 | 2020-08-01 | ClinicalTrials.gov |
| NCT03891199 | Two Year Study With Robotic-Arm Assisted Hip Surgery. | Na | Surgery | Completed | 2019-04-08 | 2020-08-01 | ClinicalTrials.gov |
| NCT03891199 | Two Year Study With Robotic-Arm Assisted Hip Surgery. | Na | Surgery | Completed | 2019-04-08 | 2020-08-01 | ClinicalTrials.gov |
| NCT03891199 | Two Year Study With Robotic-Arm Assisted Hip Surgery. | Na | Surgery | Completed | 2019-04-08 | 2020-08-01 | ClinicalTrials.gov |
| NCT03891199 | Two Year Study With Robotic-Arm Assisted Hip Surgery. | Na | Surgery | Completed | 2019-04-08 | 2020-08-01 | ClinicalTrials.gov |
| NCT03898544 | Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA | — | Knee Arthroplasty, Total | Completed | 2019-03-18 | 2020-09-10 | ClinicalTrials.gov |
| NCT03898544 | Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA | — | Knee Arthroplasty, Total | Completed | 2019-03-18 | 2020-09-10 | ClinicalTrials.gov |
| NCT03898544 | Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA | — | Knee Arthroplasty, Total | Completed | 2019-03-18 | 2020-09-10 | ClinicalTrials.gov |
| NCT03898544 | Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA | — | Knee Arthroplasty, Total | Completed | 2019-03-18 | 2020-09-10 | ClinicalTrials.gov |
| NCT03898544 | Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA | — | Knee Arthroplasty, Total | Completed | 2019-03-18 | 2020-09-10 | ClinicalTrials.gov |
| NCT03898544 | Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA | — | Knee Arthroplasty, Total | Completed | 2019-03-18 | 2020-09-10 | ClinicalTrials.gov |
| NCT03554850 | Trevo® Retriever Registry (China) | — | Real World Data in China | Completed | 2019-01-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT03554850 | Trevo® Retriever Registry (China) | — | Real World Data in China | Completed | 2019-01-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT03554850 | Trevo® Retriever Registry (China) | — | Real World Data in China | Completed | 2019-01-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT03554850 | Trevo® Retriever Registry (China) | — | Real World Data in China | Completed | 2019-01-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT03554850 | Trevo® Retriever Registry (China) | — | Real World Data in China | Completed | 2019-01-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT03554850 | Trevo® Retriever Registry (China) | — | Real World Data in China | Completed | 2019-01-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT03845491 | ASSIST Registry Studying Various Operator Techniques | — | Ischemic Stroke | Completed | 2019-01-24 | 2023-01-25 | ClinicalTrials.gov |
| NCT03845491 | ASSIST Registry Studying Various Operator Techniques | — | Ischemic Stroke | Completed | 2019-01-24 | 2023-01-25 | ClinicalTrials.gov |
| NCT03845491 | ASSIST Registry Studying Various Operator Techniques | — | Ischemic Stroke | Completed | 2019-01-24 | 2023-01-25 | ClinicalTrials.gov |
| NCT03845491 | ASSIST Registry Studying Various Operator Techniques | — | Ischemic Stroke | Completed | 2019-01-24 | 2023-01-25 | ClinicalTrials.gov |
| NCT03845491 | ASSIST Registry Studying Various Operator Techniques | — | Ischemic Stroke | Completed | 2019-01-24 | 2023-01-25 | ClinicalTrials.gov |
| NCT03845491 | ASSIST Registry Studying Various Operator Techniques | — | Ischemic Stroke | Completed | 2019-01-24 | 2023-01-25 | ClinicalTrials.gov |
| NCT04772625 | Failure Analysis of Patellofemoral Arthroplasty | — | Patellofemoral Osteoarthritis | Active_Not_Recruiting | 2019-01-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT04772625 | Failure Analysis of Patellofemoral Arthroplasty | — | Patellofemoral Osteoarthritis | Active_Not_Recruiting | 2019-01-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT04772625 | Failure Analysis of Patellofemoral Arthroplasty | — | Patellofemoral Osteoarthritis | Active_Not_Recruiting | 2019-01-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT04772625 | Failure Analysis of Patellofemoral Arthroplasty | — | Patellofemoral Osteoarthritis | Active_Not_Recruiting | 2019-01-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT04772625 | Failure Analysis of Patellofemoral Arthroplasty | — | Patellofemoral Osteoarthritis | Active_Not_Recruiting | 2019-01-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT04772625 | Failure Analysis of Patellofemoral Arthroplasty | — | Patellofemoral Osteoarthritis | Active_Not_Recruiting | 2019-01-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT04092153 | Mako Functionally Aligned Total Knee Arthroplasty vs Mako Mechanically Aligned … | Na | Osteo Arthritis Knee | Completed | 2018-12-28 | 2025-02-06 | ClinicalTrials.gov |
| NCT04092153 | Mako Functionally Aligned Total Knee Arthroplasty vs Mako Mechanically Aligned … | Na | Osteo Arthritis Knee | Completed | 2018-12-28 | 2025-02-06 | ClinicalTrials.gov |
| NCT04092153 | Mako Functionally Aligned Total Knee Arthroplasty vs Mako Mechanically Aligned … | Na | Osteo Arthritis Knee | Completed | 2018-12-28 | 2025-02-06 | ClinicalTrials.gov |
| NCT04092153 | Mako Functionally Aligned Total Knee Arthroplasty vs Mako Mechanically Aligned … | Na | Osteo Arthritis Knee | Completed | 2018-12-28 | 2025-02-06 | ClinicalTrials.gov |
| NCT04092153 | Mako Functionally Aligned Total Knee Arthroplasty vs Mako Mechanically Aligned … | Na | Osteo Arthritis Knee | Completed | 2018-12-28 | 2025-02-06 | ClinicalTrials.gov |
| NCT04092153 | Mako Functionally Aligned Total Knee Arthroplasty vs Mako Mechanically Aligned … | Na | Osteo Arthritis Knee | Completed | 2018-12-28 | 2025-02-06 | ClinicalTrials.gov |
| NCT03196011 | Traditional Versus Alternative Alignment in TKR | Na | Osteo Arthritis Knee | Active_Not_Recruiting | 2018-10-23 | 2025-12-31 | ClinicalTrials.gov |
| NCT03196011 | Traditional Versus Alternative Alignment in TKR | Na | Osteo Arthritis Knee | Active_Not_Recruiting | 2018-10-23 | 2025-12-31 | ClinicalTrials.gov |
| NCT03196011 | Traditional Versus Alternative Alignment in TKR | Na | Osteo Arthritis Knee | Active_Not_Recruiting | 2018-10-23 | 2025-12-31 | ClinicalTrials.gov |
| NCT03196011 | Traditional Versus Alternative Alignment in TKR | Na | Osteo Arthritis Knee | Active_Not_Recruiting | 2018-10-23 | 2025-12-31 | ClinicalTrials.gov |
| NCT03196011 | Traditional Versus Alternative Alignment in TKR | Na | Osteo Arthritis Knee | Active_Not_Recruiting | 2018-10-23 | 2025-12-31 | ClinicalTrials.gov |
| NCT03196011 | Traditional Versus Alternative Alignment in TKR | Na | Osteo Arthritis Knee | Active_Not_Recruiting | 2018-10-23 | 2025-12-31 | ClinicalTrials.gov |
| NCT03263117 | SEdation Versus General Anesthesia for Endovascular Therapy in Acute Ischemic S… | Phase4 | Stroke | Completed | 2018-07-01 | 2023-04-22 | ClinicalTrials.gov |
| NCT03354195 | MAKO-Uni-Knee Arthroplasty Clinical Outcomes and Function | Na | Clinical Outcomes | Completed | 2018-07-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT03354195 | MAKO-Uni-Knee Arthroplasty Clinical Outcomes and Function | Na | Clinical Outcomes | Completed | 2018-07-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT03263117 | SEdation Versus General Anesthesia for Endovascular Therapy in Acute Ischemic S… | Phase4 | Stroke | Completed | 2018-07-01 | 2023-04-22 | ClinicalTrials.gov |
| NCT03263117 | SEdation Versus General Anesthesia for Endovascular Therapy in Acute Ischemic S… | Phase4 | Stroke | Completed | 2018-07-01 | 2023-04-22 | ClinicalTrials.gov |
| NCT03263117 | SEdation Versus General Anesthesia for Endovascular Therapy in Acute Ischemic S… | Phase4 | Stroke | Completed | 2018-07-01 | 2023-04-22 | ClinicalTrials.gov |
| NCT03263117 | SEdation Versus General Anesthesia for Endovascular Therapy in Acute Ischemic S… | Phase4 | Stroke | Completed | 2018-07-01 | 2023-04-22 | ClinicalTrials.gov |
| NCT03263117 | SEdation Versus General Anesthesia for Endovascular Therapy in Acute Ischemic S… | Phase4 | Stroke | Completed | 2018-07-01 | 2023-04-22 | ClinicalTrials.gov |
| NCT03354195 | MAKO-Uni-Knee Arthroplasty Clinical Outcomes and Function | Na | Clinical Outcomes | Completed | 2018-07-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT03354195 | MAKO-Uni-Knee Arthroplasty Clinical Outcomes and Function | Na | Clinical Outcomes | Completed | 2018-07-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT03354195 | MAKO-Uni-Knee Arthroplasty Clinical Outcomes and Function | Na | Clinical Outcomes | Completed | 2018-07-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT03354195 | MAKO-Uni-Knee Arthroplasty Clinical Outcomes and Function | Na | Clinical Outcomes | Completed | 2018-07-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT03575975 | 3D X-ray Motion Analysis of Ankle-foot Motion After Total Ankle Arthroplasty | — | Ankle Arthroplasty | Terminated | 2018-05-30 | 2020-04-16 | ClinicalTrials.gov |
| NCT03575975 | 3D X-ray Motion Analysis of Ankle-foot Motion After Total Ankle Arthroplasty | — | Ankle Arthroplasty | Terminated | 2018-05-30 | 2020-04-16 | ClinicalTrials.gov |
| NCT03575975 | 3D X-ray Motion Analysis of Ankle-foot Motion After Total Ankle Arthroplasty | — | Ankle Arthroplasty | Terminated | 2018-05-30 | 2020-04-16 | ClinicalTrials.gov |
| NCT03575975 | 3D X-ray Motion Analysis of Ankle-foot Motion After Total Ankle Arthroplasty | — | Ankle Arthroplasty | Terminated | 2018-05-30 | 2020-04-16 | ClinicalTrials.gov |
| NCT03575975 | 3D X-ray Motion Analysis of Ankle-foot Motion After Total Ankle Arthroplasty | — | Ankle Arthroplasty | Terminated | 2018-05-30 | 2020-04-16 | ClinicalTrials.gov |
| NCT03575975 | 3D X-ray Motion Analysis of Ankle-foot Motion After Total Ankle Arthroplasty | — | Ankle Arthroplasty | Terminated | 2018-05-30 | 2020-04-16 | ClinicalTrials.gov |
| NCT03499028 | Improvement of Patient Satisfaction and Clinical Outcomes Using JointCOACH | Na | Arthroplasty, Replacement, Hip | Completed | 2018-05-01 | 2020-06-30 | ClinicalTrials.gov |
| NCT03499028 | Improvement of Patient Satisfaction and Clinical Outcomes Using JointCOACH | Na | Arthroplasty, Replacement, Hip | Completed | 2018-05-01 | 2020-06-30 | ClinicalTrials.gov |
| NCT03499028 | Improvement of Patient Satisfaction and Clinical Outcomes Using JointCOACH | Na | Arthroplasty, Replacement, Hip | Completed | 2018-05-01 | 2020-06-30 | ClinicalTrials.gov |
| NCT03499028 | Improvement of Patient Satisfaction and Clinical Outcomes Using JointCOACH | Na | Arthroplasty, Replacement, Hip | Completed | 2018-05-01 | 2020-06-30 | ClinicalTrials.gov |
| NCT03499028 | Improvement of Patient Satisfaction and Clinical Outcomes Using JointCOACH | Na | Arthroplasty, Replacement, Hip | Completed | 2018-05-01 | 2020-06-30 | ClinicalTrials.gov |
| NCT03499028 | Improvement of Patient Satisfaction and Clinical Outcomes Using JointCOACH | Na | Arthroplasty, Replacement, Hip | Completed | 2018-05-01 | 2020-06-30 | ClinicalTrials.gov |
| NCT03566875 | Total Knee Arthroplasty Robot Assisted With MAKO™ Robotic System Compared to th… | Na | Total Knee Arthroplasty | Unknown | 2018-04-23 | 2020-09-23 | ClinicalTrials.gov |
| NCT03566875 | Total Knee Arthroplasty Robot Assisted With MAKO™ Robotic System Compared to th… | Na | Total Knee Arthroplasty | Unknown | 2018-04-23 | 2020-09-23 | ClinicalTrials.gov |
| NCT03566875 | Total Knee Arthroplasty Robot Assisted With MAKO™ Robotic System Compared to th… | Na | Total Knee Arthroplasty | Unknown | 2018-04-23 | 2020-09-23 | ClinicalTrials.gov |
| NCT03566875 | Total Knee Arthroplasty Robot Assisted With MAKO™ Robotic System Compared to th… | Na | Total Knee Arthroplasty | Unknown | 2018-04-23 | 2020-09-23 | ClinicalTrials.gov |
| NCT03566875 | Total Knee Arthroplasty Robot Assisted With MAKO™ Robotic System Compared to th… | Na | Total Knee Arthroplasty | Unknown | 2018-04-23 | 2020-09-23 | ClinicalTrials.gov |
| NCT03566875 | Total Knee Arthroplasty Robot Assisted With MAKO™ Robotic System Compared to th… | Na | Total Knee Arthroplasty | Unknown | 2018-04-23 | 2020-09-23 | ClinicalTrials.gov |
| NCT03469817 | Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and F… | Na | Chronic Hip Pain | Completed | 2018-02-26 | 2021-05-26 | ClinicalTrials.gov |
| NCT03469817 | Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and F… | Na | Chronic Hip Pain | Completed | 2018-02-26 | 2021-05-26 | ClinicalTrials.gov |
| NCT03469817 | Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and F… | Na | Chronic Hip Pain | Completed | 2018-02-26 | 2021-05-26 | ClinicalTrials.gov |
| NCT03469817 | Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and F… | Na | Chronic Hip Pain | Completed | 2018-02-26 | 2021-05-26 | ClinicalTrials.gov |
| NCT03469817 | Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and F… | Na | Chronic Hip Pain | Completed | 2018-02-26 | 2021-05-26 | ClinicalTrials.gov |
| NCT03469817 | Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and F… | Na | Chronic Hip Pain | Completed | 2018-02-26 | 2021-05-26 | ClinicalTrials.gov |
| NCT03433742 | Metal Ion Levels in Stryker Trident II Tritanium System with Modular Dual Mobil… | Na | Hip Pain | Completed | 2018-02-22 | 2024-01-11 | ClinicalTrials.gov |
| NCT03433742 | Metal Ion Levels in Stryker Trident II Tritanium System with Modular Dual Mobil… | Na | Hip Pain | Completed | 2018-02-22 | 2024-01-11 | ClinicalTrials.gov |
| NCT03433742 | Metal Ion Levels in Stryker Trident II Tritanium System with Modular Dual Mobil… | Na | Hip Pain | Completed | 2018-02-22 | 2024-01-11 | ClinicalTrials.gov |
| NCT03433742 | Metal Ion Levels in Stryker Trident II Tritanium System with Modular Dual Mobil… | Na | Hip Pain | Completed | 2018-02-22 | 2024-01-11 | ClinicalTrials.gov |
| NCT03433742 | Metal Ion Levels in Stryker Trident II Tritanium System with Modular Dual Mobil… | Na | Hip Pain | Completed | 2018-02-22 | 2024-01-11 | ClinicalTrials.gov |
| NCT03433742 | Metal Ion Levels in Stryker Trident II Tritanium System with Modular Dual Mobil… | Na | Hip Pain | Completed | 2018-02-22 | 2024-01-11 | ClinicalTrials.gov |
| NCT03272178 | Impact of Component Design and Fixation in Total Knee Arthroplasty | — | Arthroplasties, Knee Replacement | Completed | 2017-11-20 | 2021-11-15 | ClinicalTrials.gov |
| NCT03272178 | Impact of Component Design and Fixation in Total Knee Arthroplasty | — | Arthroplasties, Knee Replacement | Completed | 2017-11-20 | 2021-11-15 | ClinicalTrials.gov |
| NCT03272178 | Impact of Component Design and Fixation in Total Knee Arthroplasty | — | Arthroplasties, Knee Replacement | Completed | 2017-11-20 | 2021-11-15 | ClinicalTrials.gov |
| NCT03272178 | Impact of Component Design and Fixation in Total Knee Arthroplasty | — | Arthroplasties, Knee Replacement | Completed | 2017-11-20 | 2021-11-15 | ClinicalTrials.gov |
| NCT03272178 | Impact of Component Design and Fixation in Total Knee Arthroplasty | — | Arthroplasties, Knee Replacement | Completed | 2017-11-20 | 2021-11-15 | ClinicalTrials.gov |
| NCT03272178 | Impact of Component Design and Fixation in Total Knee Arthroplasty | — | Arthroplasties, Knee Replacement | Completed | 2017-11-20 | 2021-11-15 | ClinicalTrials.gov |
| NCT03228251 | Simulation-based Training of Rapid Evaluation and Management for Acute Stroke (… | — | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | Completed | 2017-10-16 | 2019-03-31 | ClinicalTrials.gov |
| NCT03228251 | Simulation-based Training of Rapid Evaluation and Management for Acute Stroke (… | — | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | Completed | 2017-10-16 | 2019-03-31 | ClinicalTrials.gov |
| NCT03228251 | Simulation-based Training of Rapid Evaluation and Management for Acute Stroke (… | — | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | Completed | 2017-10-16 | 2019-03-31 | ClinicalTrials.gov |
| NCT03228251 | Simulation-based Training of Rapid Evaluation and Management for Acute Stroke (… | — | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | Completed | 2017-10-16 | 2019-03-31 | ClinicalTrials.gov |
| NCT03228251 | Simulation-based Training of Rapid Evaluation and Management for Acute Stroke (… | — | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | Completed | 2017-10-16 | 2019-03-31 | ClinicalTrials.gov |
| NCT03228251 | Simulation-based Training of Rapid Evaluation and Management for Acute Stroke (… | — | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | Completed | 2017-10-16 | 2019-03-31 | ClinicalTrials.gov |
| NCT03277989 | INFINITY™Total Ankle Replacement Follow-up | — | Arthritis, Rheumatoid | Terminated | 2017-10-09 | 2023-03-31 | ClinicalTrials.gov |
| NCT03277989 | INFINITY™Total Ankle Replacement Follow-up | — | Arthritis, Rheumatoid | Terminated | 2017-10-09 | 2023-03-31 | ClinicalTrials.gov |
| NCT03277989 | INFINITY™Total Ankle Replacement Follow-up | — | Arthritis, Rheumatoid | Terminated | 2017-10-09 | 2023-03-31 | ClinicalTrials.gov |
| NCT03277989 | INFINITY™Total Ankle Replacement Follow-up | — | Arthritis, Rheumatoid | Terminated | 2017-10-09 | 2023-03-31 | ClinicalTrials.gov |
| NCT03277989 | INFINITY™Total Ankle Replacement Follow-up | — | Arthritis, Rheumatoid | Terminated | 2017-10-09 | 2023-03-31 | ClinicalTrials.gov |
| NCT03277989 | INFINITY™Total Ankle Replacement Follow-up | — | Arthritis, Rheumatoid | Terminated | 2017-10-09 | 2023-03-31 | ClinicalTrials.gov |
| NCT03184922 | Fixed Versus Adjustable Loop in ACL Reconstruction | Na | Anterior Cruciate Ligament Reconstruction | Active_Not_Recruiting | 2017-07-05 | 2026-01-31 | ClinicalTrials.gov |
| NCT03184922 | Fixed Versus Adjustable Loop in ACL Reconstruction | Na | Anterior Cruciate Ligament Reconstruction | Active_Not_Recruiting | 2017-07-05 | 2026-01-31 | ClinicalTrials.gov |
| NCT03184922 | Fixed Versus Adjustable Loop in ACL Reconstruction | Na | Anterior Cruciate Ligament Reconstruction | Active_Not_Recruiting | 2017-07-05 | 2026-01-31 | ClinicalTrials.gov |
| NCT03184922 | Fixed Versus Adjustable Loop in ACL Reconstruction | Na | Anterior Cruciate Ligament Reconstruction | Active_Not_Recruiting | 2017-07-05 | 2026-01-31 | ClinicalTrials.gov |
| NCT03184922 | Fixed Versus Adjustable Loop in ACL Reconstruction | Na | Anterior Cruciate Ligament Reconstruction | Active_Not_Recruiting | 2017-07-05 | 2026-01-31 | ClinicalTrials.gov |
| NCT03184922 | Fixed Versus Adjustable Loop in ACL Reconstruction | Na | Anterior Cruciate Ligament Reconstruction | Active_Not_Recruiting | 2017-07-05 | 2026-01-31 | ClinicalTrials.gov |
| NCT03199404 | Trevo Aspiration Proximal Flow Control Registry | — | Stroke, Ischemic | Terminated | 2017-06-06 | 2019-10-03 | ClinicalTrials.gov |
| NCT03199404 | Trevo Aspiration Proximal Flow Control Registry | — | Stroke, Ischemic | Terminated | 2017-06-06 | 2019-10-03 | ClinicalTrials.gov |
| NCT03199404 | Trevo Aspiration Proximal Flow Control Registry | — | Stroke, Ischemic | Terminated | 2017-06-06 | 2019-10-03 | ClinicalTrials.gov |
| NCT03199404 | Trevo Aspiration Proximal Flow Control Registry | — | Stroke, Ischemic | Terminated | 2017-06-06 | 2019-10-03 | ClinicalTrials.gov |
| NCT03199404 | Trevo Aspiration Proximal Flow Control Registry | — | Stroke, Ischemic | Terminated | 2017-06-06 | 2019-10-03 | ClinicalTrials.gov |
| NCT03199404 | Trevo Aspiration Proximal Flow Control Registry | — | Stroke, Ischemic | Terminated | 2017-06-06 | 2019-10-03 | ClinicalTrials.gov |
| NCT02875561 | Ultrasonic Aspiration Versus CO2 Laser Ablation for the Treatment of Vulvar Int… | Na | Vulvar Intraepithelial Neoplasia (VIN) | Completed | 2017-03-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT02875561 | Ultrasonic Aspiration Versus CO2 Laser Ablation for the Treatment of Vulvar Int… | Na | Vulvar Intraepithelial Neoplasia (VIN) | Completed | 2017-03-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT02875561 | Ultrasonic Aspiration Versus CO2 Laser Ablation for the Treatment of Vulvar Int… | Na | Vulvar Intraepithelial Neoplasia (VIN) | Completed | 2017-03-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT02875561 | Ultrasonic Aspiration Versus CO2 Laser Ablation for the Treatment of Vulvar Int… | Na | Vulvar Intraepithelial Neoplasia (VIN) | Completed | 2017-03-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT02875561 | Ultrasonic Aspiration Versus CO2 Laser Ablation for the Treatment of Vulvar Int… | Na | Vulvar Intraepithelial Neoplasia (VIN) | Completed | 2017-03-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT02875561 | Ultrasonic Aspiration Versus CO2 Laser Ablation for the Treatment of Vulvar Int… | Na | Vulvar Intraepithelial Neoplasia (VIN) | Completed | 2017-03-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT03072927 | MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study | — | Lumbar Spinal Stenosis | Recruiting | 2017-03-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT03072927 | MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study | — | Lumbar Spinal Stenosis | Recruiting | 2017-03-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT03072927 | MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study | — | Lumbar Spinal Stenosis | Recruiting | 2017-03-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT03072927 | MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study | — | Lumbar Spinal Stenosis | Recruiting | 2017-03-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT03072927 | MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study | — | Lumbar Spinal Stenosis | Recruiting | 2017-03-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT03072927 | MILD® Percutaneous Image-Guided Lumbar Decompression: A Medicare Claims Study | — | Lumbar Spinal Stenosis | Recruiting | 2017-03-10 | 2026-12-01 | ClinicalTrials.gov |
| NCT02999009 | Trident II Tritanium Acetabular Shell Outcomes Study | Na | Arthroplasty, Replacement, Hip | Active_Not_Recruiting | 2017-01-20 | 2031-03-01 | ClinicalTrials.gov |
| NCT02999009 | Trident II Tritanium Acetabular Shell Outcomes Study | Na | Arthroplasty, Replacement, Hip | Active_Not_Recruiting | 2017-01-20 | 2031-03-01 | ClinicalTrials.gov |
| NCT02999009 | Trident II Tritanium Acetabular Shell Outcomes Study | Na | Arthroplasty, Replacement, Hip | Active_Not_Recruiting | 2017-01-20 | 2031-03-01 | ClinicalTrials.gov |
| NCT02999009 | Trident II Tritanium Acetabular Shell Outcomes Study | Na | Arthroplasty, Replacement, Hip | Active_Not_Recruiting | 2017-01-20 | 2031-03-01 | ClinicalTrials.gov |
| NCT02999009 | Trident II Tritanium Acetabular Shell Outcomes Study | Na | Arthroplasty, Replacement, Hip | Active_Not_Recruiting | 2017-01-20 | 2031-03-01 | ClinicalTrials.gov |
| NCT02999009 | Trident II Tritanium Acetabular Shell Outcomes Study | Na | Arthroplasty, Replacement, Hip | Active_Not_Recruiting | 2017-01-20 | 2031-03-01 | ClinicalTrials.gov |
| NCT02783339 | Neuroform Atlas Stent for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2016-09-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02783339 | Neuroform Atlas Stent for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2016-09-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02783339 | Neuroform Atlas Stent for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2016-09-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02783339 | Neuroform Atlas Stent for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2016-09-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02783339 | Neuroform Atlas Stent for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2016-09-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02783339 | Neuroform Atlas Stent for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2016-09-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT02830997 | Total Knee Arthroplasty Guidance Systems Study | — | Osteoarthritis, Knee | Completed | 2016-07-12 | 2021-01-05 | ClinicalTrials.gov |
| NCT02830997 | Total Knee Arthroplasty Guidance Systems Study | — | Osteoarthritis, Knee | Completed | 2016-07-12 | 2021-01-05 | ClinicalTrials.gov |
| NCT02830997 | Total Knee Arthroplasty Guidance Systems Study | — | Osteoarthritis, Knee | Completed | 2016-07-12 | 2021-01-05 | ClinicalTrials.gov |
| NCT02830997 | Total Knee Arthroplasty Guidance Systems Study | — | Osteoarthritis, Knee | Completed | 2016-07-12 | 2021-01-05 | ClinicalTrials.gov |
| NCT02830997 | Total Knee Arthroplasty Guidance Systems Study | — | Osteoarthritis, Knee | Completed | 2016-07-12 | 2021-01-05 | ClinicalTrials.gov |
| NCT02830997 | Total Knee Arthroplasty Guidance Systems Study | — | Osteoarthritis, Knee | Completed | 2016-07-12 | 2021-01-05 | ClinicalTrials.gov |
| NCT03106558 | Post-Market Study of Robotic-Arm Assisted Total Knee Arthroplasty | Na | Osteoarthritis, Knee | Unknown | 2016-06-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT03106558 | Post-Market Study of Robotic-Arm Assisted Total Knee Arthroplasty | Na | Osteoarthritis, Knee | Unknown | 2016-06-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT03106558 | Post-Market Study of Robotic-Arm Assisted Total Knee Arthroplasty | Na | Osteoarthritis, Knee | Unknown | 2016-06-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT03106558 | Post-Market Study of Robotic-Arm Assisted Total Knee Arthroplasty | Na | Osteoarthritis, Knee | Unknown | 2016-06-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT03106558 | Post-Market Study of Robotic-Arm Assisted Total Knee Arthroplasty | Na | Osteoarthritis, Knee | Unknown | 2016-06-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT03106558 | Post-Market Study of Robotic-Arm Assisted Total Knee Arthroplasty | Na | Osteoarthritis, Knee | Unknown | 2016-06-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT02779504 | Post Market Clinical Follow Up Study for Evaluation of Agluna® METS | — | Infection | Completed | 2016-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779504 | Post Market Clinical Follow Up Study for Evaluation of Agluna® METS | — | Infection | Completed | 2016-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779504 | Post Market Clinical Follow Up Study for Evaluation of Agluna® METS | — | Infection | Completed | 2016-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779504 | Post Market Clinical Follow Up Study for Evaluation of Agluna® METS | — | Infection | Completed | 2016-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779504 | Post Market Clinical Follow Up Study for Evaluation of Agluna® METS | — | Infection | Completed | 2016-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02779504 | Post Market Clinical Follow Up Study for Evaluation of Agluna® METS | — | Infection | Completed | 2016-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT05659329 | Retrospective Simplex High Viscosity (HV) Bone Cement Study | — | Arthritis Knee | Completed | 2016-04-25 | 2022-09-27 | ClinicalTrials.gov |
| NCT05659329 | Retrospective Simplex High Viscosity (HV) Bone Cement Study | — | Arthritis Knee | Completed | 2016-04-25 | 2022-09-27 | ClinicalTrials.gov |
| NCT05659329 | Retrospective Simplex High Viscosity (HV) Bone Cement Study | — | Arthritis Knee | Completed | 2016-04-25 | 2022-09-27 | ClinicalTrials.gov |
| NCT05659329 | Retrospective Simplex High Viscosity (HV) Bone Cement Study | — | Arthritis Knee | Completed | 2016-04-25 | 2022-09-27 | ClinicalTrials.gov |
| NCT05659329 | Retrospective Simplex High Viscosity (HV) Bone Cement Study | — | Arthritis Knee | Completed | 2016-04-25 | 2022-09-27 | ClinicalTrials.gov |
| NCT05659329 | Retrospective Simplex High Viscosity (HV) Bone Cement Study | — | Arthritis Knee | Completed | 2016-04-25 | 2022-09-27 | ClinicalTrials.gov |
| NCT02768597 | Comparing The Outcome of Large-Diameter vs Small-Diameter Glenospheres in Prima… | Na | Glenohumeral Joint Degeneration | Completed | 2016-04-01 | 2022-12-15 | ClinicalTrials.gov |
| NCT02768597 | Comparing The Outcome of Large-Diameter vs Small-Diameter Glenospheres in Prima… | Na | Glenohumeral Joint Degeneration | Completed | 2016-04-01 | 2022-12-15 | ClinicalTrials.gov |
| NCT02768597 | Comparing The Outcome of Large-Diameter vs Small-Diameter Glenospheres in Prima… | Na | Glenohumeral Joint Degeneration | Completed | 2016-04-01 | 2022-12-15 | ClinicalTrials.gov |
| NCT02768597 | Comparing The Outcome of Large-Diameter vs Small-Diameter Glenospheres in Prima… | Na | Glenohumeral Joint Degeneration | Completed | 2016-04-01 | 2022-12-15 | ClinicalTrials.gov |
| NCT02768597 | Comparing The Outcome of Large-Diameter vs Small-Diameter Glenospheres in Prima… | Na | Glenohumeral Joint Degeneration | Completed | 2016-04-01 | 2022-12-15 | ClinicalTrials.gov |
| NCT02768597 | Comparing The Outcome of Large-Diameter vs Small-Diameter Glenospheres in Prima… | Na | Glenohumeral Joint Degeneration | Completed | 2016-04-01 | 2022-12-15 | ClinicalTrials.gov |
| NCT02618031 | The Capillary Index Score Trial | Phase1 | Acute Stroke | Completed | 2016-03-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02618031 | The Capillary Index Score Trial | Phase1 | Acute Stroke | Completed | 2016-03-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02618031 | The Capillary Index Score Trial | Phase1 | Acute Stroke | Completed | 2016-03-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02618031 | The Capillary Index Score Trial | Phase1 | Acute Stroke | Completed | 2016-03-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02618031 | The Capillary Index Score Trial | Phase1 | Acute Stroke | Completed | 2016-03-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT02618031 | The Capillary Index Score Trial | Phase1 | Acute Stroke | Completed | 2016-03-01 | 2018-12-31 | ClinicalTrials.gov |
| NCT03077022 | Femoroacetabular Impingement (FAI): The Effectiveness of Physical Therapy | — | Femoroacetabular Impingement | Withdrawn | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT03077022 | Femoroacetabular Impingement (FAI): The Effectiveness of Physical Therapy | — | Femoroacetabular Impingement | Withdrawn | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT03077022 | Femoroacetabular Impingement (FAI): The Effectiveness of Physical Therapy | — | Femoroacetabular Impingement | Withdrawn | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT03077022 | Femoroacetabular Impingement (FAI): The Effectiveness of Physical Therapy | — | Femoroacetabular Impingement | Withdrawn | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT03077022 | Femoroacetabular Impingement (FAI): The Effectiveness of Physical Therapy | — | Femoroacetabular Impingement | Withdrawn | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT03077022 | Femoroacetabular Impingement (FAI): The Effectiveness of Physical Therapy | — | Femoroacetabular Impingement | Withdrawn | 2016-02-01 | 2018-02-01 | ClinicalTrials.gov |
| NCT02446587 | Optimizing Patient's Selection for Endovascular Treatment in Acute Ischemic Str… | — | Stroke | Completed | 2016-01-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02403453 | RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Pati… | — | Radiculopathy | Terminated | 2016-01-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT02446587 | Optimizing Patient's Selection for Endovascular Treatment in Acute Ischemic Str… | — | Stroke | Completed | 2016-01-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02403453 | RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Pati… | — | Radiculopathy | Terminated | 2016-01-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT02403453 | RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Pati… | — | Radiculopathy | Terminated | 2016-01-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT02403453 | RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Pati… | — | Radiculopathy | Terminated | 2016-01-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT02403453 | RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Pati… | — | Radiculopathy | Terminated | 2016-01-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT02403453 | RHINE™ Cervical Disc Clinical Study: A Prospective Observational Study for Pati… | — | Radiculopathy | Terminated | 2016-01-01 | 2023-03-01 | ClinicalTrials.gov |
| NCT02446587 | Optimizing Patient's Selection for Endovascular Treatment in Acute Ischemic Str… | — | Stroke | Completed | 2016-01-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02446587 | Optimizing Patient's Selection for Endovascular Treatment in Acute Ischemic Str… | — | Stroke | Completed | 2016-01-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02446587 | Optimizing Patient's Selection for Endovascular Treatment in Acute Ischemic Str… | — | Stroke | Completed | 2016-01-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02446587 | Optimizing Patient's Selection for Endovascular Treatment in Acute Ischemic Str… | — | Stroke | Completed | 2016-01-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02525783 | Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty | — | Osteoarthritis | Completed | 2015-12-01 | 2022-10-07 | ClinicalTrials.gov |
| NCT02525783 | Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty | — | Osteoarthritis | Completed | 2015-12-01 | 2022-10-07 | ClinicalTrials.gov |
| NCT02525783 | Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty | — | Osteoarthritis | Completed | 2015-12-01 | 2022-10-07 | ClinicalTrials.gov |
| NCT02525783 | Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty | — | Osteoarthritis | Completed | 2015-12-01 | 2022-10-07 | ClinicalTrials.gov |
| NCT02525783 | Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty | — | Osteoarthritis | Completed | 2015-12-01 | 2022-10-07 | ClinicalTrials.gov |
| NCT02525783 | Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty | — | Osteoarthritis | Completed | 2015-12-01 | 2022-10-07 | ClinicalTrials.gov |
| NCT02578446 | Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in To… | Na | Arthroplasty | Active_Not_Recruiting | 2015-10-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT02578446 | Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in To… | Na | Arthroplasty | Active_Not_Recruiting | 2015-10-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT02578446 | Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in To… | Na | Arthroplasty | Active_Not_Recruiting | 2015-10-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT02578446 | Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in To… | Na | Arthroplasty | Active_Not_Recruiting | 2015-10-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT02578446 | Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in To… | Na | Arthroplasty | Active_Not_Recruiting | 2015-10-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT02578446 | Uncemented Tritanium Compared With Cemented Metal-backed Tibia Components in To… | Na | Arthroplasty | Active_Not_Recruiting | 2015-10-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT02521103 | Triathlon Tritanium Cone Augments Outcomes Study | Na | Arthroplasty | Active_Not_Recruiting | 2015-08-01 | 2028-03-31 | ClinicalTrials.gov |
| NCT02521103 | Triathlon Tritanium Cone Augments Outcomes Study | Na | Arthroplasty | Active_Not_Recruiting | 2015-08-01 | 2028-03-31 | ClinicalTrials.gov |
| NCT02521103 | Triathlon Tritanium Cone Augments Outcomes Study | Na | Arthroplasty | Active_Not_Recruiting | 2015-08-01 | 2028-03-31 | ClinicalTrials.gov |
| NCT02521103 | Triathlon Tritanium Cone Augments Outcomes Study | Na | Arthroplasty | Active_Not_Recruiting | 2015-08-01 | 2028-03-31 | ClinicalTrials.gov |
| NCT02521103 | Triathlon Tritanium Cone Augments Outcomes Study | Na | Arthroplasty | Active_Not_Recruiting | 2015-08-01 | 2028-03-31 | ClinicalTrials.gov |
| NCT02521103 | Triathlon Tritanium Cone Augments Outcomes Study | Na | Arthroplasty | Active_Not_Recruiting | 2015-08-01 | 2028-03-31 | ClinicalTrials.gov |
| NCT02281721 | Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data Collec… | — | Cerebral Aneurysm | Terminated | 2015-03-18 | 2019-12-01 | ClinicalTrials.gov |
| NCT02281721 | Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data Collec… | — | Cerebral Aneurysm | Terminated | 2015-03-18 | 2019-12-01 | ClinicalTrials.gov |
| NCT02281721 | Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data Collec… | — | Cerebral Aneurysm | Terminated | 2015-03-18 | 2019-12-01 | ClinicalTrials.gov |
| NCT02281721 | Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data Collec… | — | Cerebral Aneurysm | Terminated | 2015-03-18 | 2019-12-01 | ClinicalTrials.gov |
| NCT02281721 | Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data Collec… | — | Cerebral Aneurysm | Terminated | 2015-03-18 | 2019-12-01 | ClinicalTrials.gov |
| NCT02281721 | Surpass Flow Diverter for Intracranial Aneurysms: SURMOUNT Registry Data Collec… | — | Cerebral Aneurysm | Terminated | 2015-03-18 | 2019-12-01 | ClinicalTrials.gov |
| NCT02373761 | A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the T… | — | Osteoarthritis of the Knee | Unknown | 2015-02-01 | — | ClinicalTrials.gov |
| NCT02373761 | A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the T… | — | Osteoarthritis of the Knee | Unknown | 2015-02-01 | — | ClinicalTrials.gov |
| NCT02373761 | A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the T… | — | Osteoarthritis of the Knee | Unknown | 2015-02-01 | — | ClinicalTrials.gov |
| NCT02373761 | A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the T… | — | Osteoarthritis of the Knee | Unknown | 2015-02-01 | — | ClinicalTrials.gov |
| NCT02373761 | A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the T… | — | Osteoarthritis of the Knee | Unknown | 2015-02-01 | — | ClinicalTrials.gov |
| NCT02373761 | A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the T… | — | Osteoarthritis of the Knee | Unknown | 2015-02-01 | — | ClinicalTrials.gov |
| NCT05267964 | Trapeziometacarpal Prosthesis vs. Resection-Interposition Arthroplasty | Na | Arthropathy of Hand | Unknown | 2014-11-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT05267964 | Trapeziometacarpal Prosthesis vs. Resection-Interposition Arthroplasty | Na | Arthropathy of Hand | Unknown | 2014-11-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT05267964 | Trapeziometacarpal Prosthesis vs. Resection-Interposition Arthroplasty | Na | Arthropathy of Hand | Unknown | 2014-11-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT05267964 | Trapeziometacarpal Prosthesis vs. Resection-Interposition Arthroplasty | Na | Arthropathy of Hand | Unknown | 2014-11-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT05267964 | Trapeziometacarpal Prosthesis vs. Resection-Interposition Arthroplasty | Na | Arthropathy of Hand | Unknown | 2014-11-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT05267964 | Trapeziometacarpal Prosthesis vs. Resection-Interposition Arthroplasty | Na | Arthropathy of Hand | Unknown | 2014-11-01 | 2022-04-01 | ClinicalTrials.gov |
| NCT02155712 | Triathlon Tritanium Knee Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2014-10-01 | 2023-03-11 | ClinicalTrials.gov |
| NCT02155712 | Triathlon Tritanium Knee Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2014-10-01 | 2023-03-11 | ClinicalTrials.gov |
| NCT02155712 | Triathlon Tritanium Knee Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2014-10-01 | 2023-03-11 | ClinicalTrials.gov |
| NCT02155712 | Triathlon Tritanium Knee Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2014-10-01 | 2023-03-11 | ClinicalTrials.gov |
| NCT02155712 | Triathlon Tritanium Knee Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2014-10-01 | 2023-03-11 | ClinicalTrials.gov |
| NCT02155712 | Triathlon Tritanium Knee Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2014-10-01 | 2023-03-11 | ClinicalTrials.gov |
| NCT02142283 | Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoi… | Na | Ischemic Stroke | Completed | 2014-07-01 | 2017-05-15 | ClinicalTrials.gov |
| NCT02142283 | Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoi… | Na | Ischemic Stroke | Completed | 2014-07-01 | 2017-05-15 | ClinicalTrials.gov |
| NCT02142283 | Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoi… | Na | Ischemic Stroke | Completed | 2014-07-01 | 2017-05-15 | ClinicalTrials.gov |
| NCT02190435 | Computer-Assisted Navigation for Intramedullary Nail Fixation of Intertrochante… | Na | Intertrochanteric Femur Fractures | Completed | 2014-07-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02142283 | Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoi… | Na | Ischemic Stroke | Completed | 2014-07-01 | 2017-05-15 | ClinicalTrials.gov |
| NCT02190435 | Computer-Assisted Navigation for Intramedullary Nail Fixation of Intertrochante… | Na | Intertrochanteric Femur Fractures | Completed | 2014-07-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02142283 | Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoi… | Na | Ischemic Stroke | Completed | 2014-07-01 | 2017-05-15 | ClinicalTrials.gov |
| NCT02190435 | Computer-Assisted Navigation for Intramedullary Nail Fixation of Intertrochante… | Na | Intertrochanteric Femur Fractures | Completed | 2014-07-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02190435 | Computer-Assisted Navigation for Intramedullary Nail Fixation of Intertrochante… | Na | Intertrochanteric Femur Fractures | Completed | 2014-07-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02190435 | Computer-Assisted Navigation for Intramedullary Nail Fixation of Intertrochante… | Na | Intertrochanteric Femur Fractures | Completed | 2014-07-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02142283 | Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoi… | Na | Ischemic Stroke | Completed | 2014-07-01 | 2017-05-15 | ClinicalTrials.gov |
| NCT02190435 | Computer-Assisted Navigation for Intramedullary Nail Fixation of Intertrochante… | Na | Intertrochanteric Femur Fractures | Completed | 2014-07-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02047955 | Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Sh… | — | Shoulder Arthroplasty and Fracture Repair | Terminated | 2014-03-01 | 2024-10-16 | ClinicalTrials.gov |
| NCT02047955 | Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Sh… | — | Shoulder Arthroplasty and Fracture Repair | Terminated | 2014-03-01 | 2024-10-16 | ClinicalTrials.gov |
| NCT02047955 | Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Sh… | — | Shoulder Arthroplasty and Fracture Repair | Terminated | 2014-03-01 | 2024-10-16 | ClinicalTrials.gov |
| NCT02047955 | Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Sh… | — | Shoulder Arthroplasty and Fracture Repair | Terminated | 2014-03-01 | 2024-10-16 | ClinicalTrials.gov |
| NCT02047955 | Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Sh… | — | Shoulder Arthroplasty and Fracture Repair | Terminated | 2014-03-01 | 2024-10-16 | ClinicalTrials.gov |
| NCT02047955 | Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Sh… | — | Shoulder Arthroplasty and Fracture Repair | Terminated | 2014-03-01 | 2024-10-16 | ClinicalTrials.gov |
| NCT02034058 | Post Market Surveillance Study of the Wingspan Stent System | Na | Intracranial Atherosclerosis | Completed | 2013-12-01 | 2019-08-01 | ClinicalTrials.gov |
| NCT02034058 | Post Market Surveillance Study of the Wingspan Stent System | Na | Intracranial Atherosclerosis | Completed | 2013-12-01 | 2019-08-01 | ClinicalTrials.gov |
| NCT01949779 | TransForm™ Occlusion Balloon Catheter Registry | — | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01949779 | TransForm™ Occlusion Balloon Catheter Registry | — | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02034058 | Post Market Surveillance Study of the Wingspan Stent System | Na | Intracranial Atherosclerosis | Completed | 2013-12-01 | 2019-08-01 | ClinicalTrials.gov |
| NCT02034058 | Post Market Surveillance Study of the Wingspan Stent System | Na | Intracranial Atherosclerosis | Completed | 2013-12-01 | 2019-08-01 | ClinicalTrials.gov |
| NCT01949779 | TransForm™ Occlusion Balloon Catheter Registry | — | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01949779 | TransForm™ Occlusion Balloon Catheter Registry | — | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02034058 | Post Market Surveillance Study of the Wingspan Stent System | Na | Intracranial Atherosclerosis | Completed | 2013-12-01 | 2019-08-01 | ClinicalTrials.gov |
| NCT01949779 | TransForm™ Occlusion Balloon Catheter Registry | — | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02034058 | Post Market Surveillance Study of the Wingspan Stent System | Na | Intracranial Atherosclerosis | Completed | 2013-12-01 | 2019-08-01 | ClinicalTrials.gov |
| NCT01949779 | TransForm™ Occlusion Balloon Catheter Registry | — | Intracranial Aneurysms | Completed | 2013-12-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02040259 | Trevo® Retriever Registry Post Market Surveillance | — | Ischemic Stroke | Completed | 2013-11-25 | 2017-12-28 | ClinicalTrials.gov |
| NCT02040259 | Trevo® Retriever Registry Post Market Surveillance | — | Ischemic Stroke | Completed | 2013-11-25 | 2017-12-28 | ClinicalTrials.gov |
| NCT02040259 | Trevo® Retriever Registry Post Market Surveillance | — | Ischemic Stroke | Completed | 2013-11-25 | 2017-12-28 | ClinicalTrials.gov |
| NCT02040259 | Trevo® Retriever Registry Post Market Surveillance | — | Ischemic Stroke | Completed | 2013-11-25 | 2017-12-28 | ClinicalTrials.gov |
| NCT02040259 | Trevo® Retriever Registry Post Market Surveillance | — | Ischemic Stroke | Completed | 2013-11-25 | 2017-12-28 | ClinicalTrials.gov |
| NCT02040259 | Trevo® Retriever Registry Post Market Surveillance | — | Ischemic Stroke | Completed | 2013-11-25 | 2017-12-28 | ClinicalTrials.gov |
| NCT02657772 | Ultra Coils From Start to Finish for the Endovascular Repair of Small Intracran… | — | Intracranial Aneurysms | Completed | 2013-11-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02657772 | Ultra Coils From Start to Finish for the Endovascular Repair of Small Intracran… | — | Intracranial Aneurysms | Completed | 2013-11-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02657772 | Ultra Coils From Start to Finish for the Endovascular Repair of Small Intracran… | — | Intracranial Aneurysms | Completed | 2013-11-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02657772 | Ultra Coils From Start to Finish for the Endovascular Repair of Small Intracran… | — | Intracranial Aneurysms | Completed | 2013-11-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02657772 | Ultra Coils From Start to Finish for the Endovascular Repair of Small Intracran… | — | Intracranial Aneurysms | Completed | 2013-11-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02657772 | Ultra Coils From Start to Finish for the Endovascular Repair of Small Intracran… | — | Intracranial Aneurysms | Completed | 2013-11-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02062437 | Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Fri… | — | Hip Replacement | Completed | 2013-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT02062437 | Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Fri… | — | Hip Replacement | Completed | 2013-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT02062437 | Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Fri… | — | Hip Replacement | Completed | 2013-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT02062437 | Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Fri… | — | Hip Replacement | Completed | 2013-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT02062437 | Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Fri… | — | Hip Replacement | Completed | 2013-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT02062437 | Clinical and Radiological Results of Total Hip Arthroplasty Using a Ceramic Fri… | — | Hip Replacement | Completed | 2013-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01917929 | Secur-Fit Advanced Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2013-08-15 | 2024-06-13 | ClinicalTrials.gov |
| NCT01917929 | Secur-Fit Advanced Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2013-08-15 | 2024-06-13 | ClinicalTrials.gov |
| NCT01917929 | Secur-Fit Advanced Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2013-08-15 | 2024-06-13 | ClinicalTrials.gov |
| NCT01917929 | Secur-Fit Advanced Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2013-08-15 | 2024-06-13 | ClinicalTrials.gov |
| NCT01917929 | Secur-Fit Advanced Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2013-08-15 | 2024-06-13 | ClinicalTrials.gov |
| NCT01917929 | Secur-Fit Advanced Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2013-08-15 | 2024-06-13 | ClinicalTrials.gov |
| NCT02070627 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy -- U… | Phase1 | Acute Cholecystitis | Completed | 2013-07-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070627 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy -- U… | Phase1 | Acute Cholecystitis | Completed | 2013-07-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070627 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy -- U… | Phase1 | Acute Cholecystitis | Completed | 2013-07-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070627 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy -- U… | Phase1 | Acute Cholecystitis | Completed | 2013-07-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070627 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy -- U… | Phase1 | Acute Cholecystitis | Completed | 2013-07-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070627 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy -- U… | Phase1 | Acute Cholecystitis | Completed | 2013-07-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01864434 | In Vivo Kinematics Comparison of Stryker or Zimmer Total Knee Arthroplasty | — | Knee Prosthesis | Completed | 2013-06-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01864434 | In Vivo Kinematics Comparison of Stryker or Zimmer Total Knee Arthroplasty | — | Knee Prosthesis | Completed | 2013-06-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01864434 | In Vivo Kinematics Comparison of Stryker or Zimmer Total Knee Arthroplasty | — | Knee Prosthesis | Completed | 2013-06-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01864434 | In Vivo Kinematics Comparison of Stryker or Zimmer Total Knee Arthroplasty | — | Knee Prosthesis | Completed | 2013-06-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01864434 | In Vivo Kinematics Comparison of Stryker or Zimmer Total Knee Arthroplasty | — | Knee Prosthesis | Completed | 2013-06-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01864434 | In Vivo Kinematics Comparison of Stryker or Zimmer Total Knee Arthroplasty | — | Knee Prosthesis | Completed | 2013-06-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02062450 | Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual … | — | Primary Osteoarthritis | Completed | 2013-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02062450 | Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual … | — | Primary Osteoarthritis | Completed | 2013-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02062450 | Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual … | — | Primary Osteoarthritis | Completed | 2013-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02062450 | Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual … | — | Primary Osteoarthritis | Completed | 2013-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02062450 | Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual … | — | Primary Osteoarthritis | Completed | 2013-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02062450 | Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual … | — | Primary Osteoarthritis | Completed | 2013-05-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01923805 | Vitagel Revision Total Knee Arthroplasty | Na | Failed Total Knee Arthroplasty | Terminated | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT03668704 | Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty | — | Osteoarthritis | Active_Not_Recruiting | 2013-04-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT01845597 | Survivorship and Outcomes of Robot Assisted Medial Partial Knee Replacement | — | Unicompartmental Knee Arthroplasty | Completed | 2013-04-01 | 2022-02-28 | ClinicalTrials.gov |
| NCT01923805 | Vitagel Revision Total Knee Arthroplasty | Na | Failed Total Knee Arthroplasty | Terminated | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01845597 | Survivorship and Outcomes of Robot Assisted Medial Partial Knee Replacement | — | Unicompartmental Knee Arthroplasty | Completed | 2013-04-01 | 2022-02-28 | ClinicalTrials.gov |
| NCT03668704 | Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty | — | Osteoarthritis | Active_Not_Recruiting | 2013-04-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT03668704 | Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty | — | Osteoarthritis | Active_Not_Recruiting | 2013-04-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT01923805 | Vitagel Revision Total Knee Arthroplasty | Na | Failed Total Knee Arthroplasty | Terminated | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01923805 | Vitagel Revision Total Knee Arthroplasty | Na | Failed Total Knee Arthroplasty | Terminated | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT03668704 | Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty | — | Osteoarthritis | Active_Not_Recruiting | 2013-04-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT01923805 | Vitagel Revision Total Knee Arthroplasty | Na | Failed Total Knee Arthroplasty | Terminated | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01845597 | Survivorship and Outcomes of Robot Assisted Medial Partial Knee Replacement | — | Unicompartmental Knee Arthroplasty | Completed | 2013-04-01 | 2022-02-28 | ClinicalTrials.gov |
| NCT01845597 | Survivorship and Outcomes of Robot Assisted Medial Partial Knee Replacement | — | Unicompartmental Knee Arthroplasty | Completed | 2013-04-01 | 2022-02-28 | ClinicalTrials.gov |
| NCT03668704 | Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty | — | Osteoarthritis | Active_Not_Recruiting | 2013-04-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT03668704 | Survivorship and Outcomes of Robotic-Arm Assisted Bicompartmental Arthroplasty | — | Osteoarthritis | Active_Not_Recruiting | 2013-04-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT01845597 | Survivorship and Outcomes of Robot Assisted Medial Partial Knee Replacement | — | Unicompartmental Knee Arthroplasty | Completed | 2013-04-01 | 2022-02-28 | ClinicalTrials.gov |
| NCT01845597 | Survivorship and Outcomes of Robot Assisted Medial Partial Knee Replacement | — | Unicompartmental Knee Arthroplasty | Completed | 2013-04-01 | 2022-02-28 | ClinicalTrials.gov |
| NCT01923805 | Vitagel Revision Total Knee Arthroplasty | Na | Failed Total Knee Arthroplasty | Terminated | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01849458 | BioFiber Scaffold Post-Market Observational Study | — | Full Thickness Rotator Cuff Tear | Completed | 2013-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01849458 | BioFiber Scaffold Post-Market Observational Study | — | Full Thickness Rotator Cuff Tear | Completed | 2013-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01849458 | BioFiber Scaffold Post-Market Observational Study | — | Full Thickness Rotator Cuff Tear | Completed | 2013-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01849458 | BioFiber Scaffold Post-Market Observational Study | — | Full Thickness Rotator Cuff Tear | Completed | 2013-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01849458 | BioFiber Scaffold Post-Market Observational Study | — | Full Thickness Rotator Cuff Tear | Completed | 2013-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01849458 | BioFiber Scaffold Post-Market Observational Study | — | Full Thickness Rotator Cuff Tear | Completed | 2013-03-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02070640 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy | Na | Cholecystitis | Completed | 2013-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070640 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy | Na | Cholecystitis | Completed | 2013-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070640 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy | Na | Cholecystitis | Completed | 2013-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070640 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy | Na | Cholecystitis | Completed | 2013-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070640 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy | Na | Cholecystitis | Completed | 2013-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT02070640 | Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy | Na | Cholecystitis | Completed | 2013-01-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01716117 | Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Tr… | Na | Brain Aneurysm | Completed | 2012-10-25 | 2022-07-07 | ClinicalTrials.gov |
| NCT01716117 | Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Tr… | Na | Brain Aneurysm | Completed | 2012-10-25 | 2022-07-07 | ClinicalTrials.gov |
| NCT01716117 | Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Tr… | Na | Brain Aneurysm | Completed | 2012-10-25 | 2022-07-07 | ClinicalTrials.gov |
| NCT01716117 | Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Tr… | Na | Brain Aneurysm | Completed | 2012-10-25 | 2022-07-07 | ClinicalTrials.gov |
| NCT01716117 | Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Tr… | Na | Brain Aneurysm | Completed | 2012-10-25 | 2022-07-07 | ClinicalTrials.gov |
| NCT01716117 | Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Tr… | Na | Brain Aneurysm | Completed | 2012-10-25 | 2022-07-07 | ClinicalTrials.gov |
| NCT02525562 | Stryker NTX Registry Scorpio NRG (Re-"Energize"), Triathlon Total Knee, Triathl… | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-06-28 | 2020-05-28 | ClinicalTrials.gov |
| NCT02525562 | Stryker NTX Registry Scorpio NRG (Re-"Energize"), Triathlon Total Knee, Triathl… | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-06-28 | 2020-05-28 | ClinicalTrials.gov |
| NCT02525562 | Stryker NTX Registry Scorpio NRG (Re-"Energize"), Triathlon Total Knee, Triathl… | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-06-28 | 2020-05-28 | ClinicalTrials.gov |
| NCT02525562 | Stryker NTX Registry Scorpio NRG (Re-"Energize"), Triathlon Total Knee, Triathl… | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-06-28 | 2020-05-28 | ClinicalTrials.gov |
| NCT02525562 | Stryker NTX Registry Scorpio NRG (Re-"Energize"), Triathlon Total Knee, Triathl… | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-06-28 | 2020-05-28 | ClinicalTrials.gov |
| NCT02525562 | Stryker NTX Registry Scorpio NRG (Re-"Energize"), Triathlon Total Knee, Triathl… | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-06-28 | 2020-05-28 | ClinicalTrials.gov |
| NCT02539992 | ShapeMatch Cutting Guide Functional Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02539992 | ShapeMatch Cutting Guide Functional Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02539992 | ShapeMatch Cutting Guide Functional Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02539992 | ShapeMatch Cutting Guide Functional Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02539992 | ShapeMatch Cutting Guide Functional Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02539992 | ShapeMatch Cutting Guide Functional Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2012-05-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT00967161 | Motion Analysis of EMP Knee Versus Posterior Stabilized Knee Arthroplasty for O… | Na | Arthropathy of Knee Joint | Completed | 2012-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00967161 | Motion Analysis of EMP Knee Versus Posterior Stabilized Knee Arthroplasty for O… | Na | Arthropathy of Knee Joint | Completed | 2012-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00967161 | Motion Analysis of EMP Knee Versus Posterior Stabilized Knee Arthroplasty for O… | Na | Arthropathy of Knee Joint | Completed | 2012-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00967161 | Motion Analysis of EMP Knee Versus Posterior Stabilized Knee Arthroplasty for O… | Na | Arthropathy of Knee Joint | Completed | 2012-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00967161 | Motion Analysis of EMP Knee Versus Posterior Stabilized Knee Arthroplasty for O… | Na | Arthropathy of Knee Joint | Completed | 2012-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT00967161 | Motion Analysis of EMP Knee Versus Posterior Stabilized Knee Arthroplasty for O… | Na | Arthropathy of Knee Joint | Completed | 2012-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01380444 | Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation | Na | Femoral Neck Fractures | Completed | 2011-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT01380444 | Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation | Na | Femoral Neck Fractures | Completed | 2011-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT01380444 | Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation | Na | Femoral Neck Fractures | Completed | 2011-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT01380444 | Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation | Na | Femoral Neck Fractures | Completed | 2011-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT01380444 | Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation | Na | Femoral Neck Fractures | Completed | 2011-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT01380444 | Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation | Na | Femoral Neck Fractures | Completed | 2011-12-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT01618084 | RSA Study Using Two Types of Uncemented Acetabular Components and the Uncemente… | Phase4 | Osteoarthritis | Unknown | 2011-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01505452 | Study of Surgical Technique With Use of Single-radius Prosthesis in Total Knee … | — | Arthritis of Knee | Completed | 2011-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01618084 | RSA Study Using Two Types of Uncemented Acetabular Components and the Uncemente… | Phase4 | Osteoarthritis | Unknown | 2011-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01505452 | Study of Surgical Technique With Use of Single-radius Prosthesis in Total Knee … | — | Arthritis of Knee | Completed | 2011-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01505452 | Study of Surgical Technique With Use of Single-radius Prosthesis in Total Knee … | — | Arthritis of Knee | Completed | 2011-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01618084 | RSA Study Using Two Types of Uncemented Acetabular Components and the Uncemente… | Phase4 | Osteoarthritis | Unknown | 2011-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01618084 | RSA Study Using Two Types of Uncemented Acetabular Components and the Uncemente… | Phase4 | Osteoarthritis | Unknown | 2011-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01505452 | Study of Surgical Technique With Use of Single-radius Prosthesis in Total Knee … | — | Arthritis of Knee | Completed | 2011-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01618084 | RSA Study Using Two Types of Uncemented Acetabular Components and the Uncemente… | Phase4 | Osteoarthritis | Unknown | 2011-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01505452 | Study of Surgical Technique With Use of Single-radius Prosthesis in Total Knee … | — | Arthritis of Knee | Completed | 2011-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01618084 | RSA Study Using Two Types of Uncemented Acetabular Components and the Uncemente… | Phase4 | Osteoarthritis | Unknown | 2011-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01505452 | Study of Surgical Technique With Use of Single-radius Prosthesis in Total Knee … | — | Arthritis of Knee | Completed | 2011-11-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT03668717 | Survivorship and Outcomes of Robotic-Arm Assisted Medial Unicompartmental Knee … | — | Osteoarthritis | Active_Not_Recruiting | 2011-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT03668717 | Survivorship and Outcomes of Robotic-Arm Assisted Medial Unicompartmental Knee … | — | Osteoarthritis | Active_Not_Recruiting | 2011-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT03668717 | Survivorship and Outcomes of Robotic-Arm Assisted Medial Unicompartmental Knee … | — | Osteoarthritis | Active_Not_Recruiting | 2011-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT03668717 | Survivorship and Outcomes of Robotic-Arm Assisted Medial Unicompartmental Knee … | — | Osteoarthritis | Active_Not_Recruiting | 2011-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT03668717 | Survivorship and Outcomes of Robotic-Arm Assisted Medial Unicompartmental Knee … | — | Osteoarthritis | Active_Not_Recruiting | 2011-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT03668717 | Survivorship and Outcomes of Robotic-Arm Assisted Medial Unicompartmental Knee … | — | Osteoarthritis | Active_Not_Recruiting | 2011-10-01 | 2026-04-01 | ClinicalTrials.gov |
| NCT02525588 | Polyethylene Wear Study on the Triathlon Total Knee Prosthesis | Na | Arthroplasty, Replacement, Knee | Completed | 2011-09-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT02525588 | Polyethylene Wear Study on the Triathlon Total Knee Prosthesis | Na | Arthroplasty, Replacement, Knee | Completed | 2011-09-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT02525588 | Polyethylene Wear Study on the Triathlon Total Knee Prosthesis | Na | Arthroplasty, Replacement, Knee | Completed | 2011-09-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT02525588 | Polyethylene Wear Study on the Triathlon Total Knee Prosthesis | Na | Arthroplasty, Replacement, Knee | Completed | 2011-09-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT02525588 | Polyethylene Wear Study on the Triathlon Total Knee Prosthesis | Na | Arthroplasty, Replacement, Knee | Completed | 2011-09-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT02525588 | Polyethylene Wear Study on the Triathlon Total Knee Prosthesis | Na | Arthroplasty, Replacement, Knee | Completed | 2011-09-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT03668691 | Clinical Outcomes of Joint Arthroplasty | — | Osteoarthritis, Knee | Active_Not_Recruiting | 2011-07-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT01063751 | Tritanium® Primary Acetabular Shell Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-07-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT01390038 | Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder Arthroplasty | Phase3 | Primary Generalized (Osteo)Arthritis | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01390038 | Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder Arthroplasty | Phase3 | Primary Generalized (Osteo)Arthritis | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT03668691 | Clinical Outcomes of Joint Arthroplasty | — | Osteoarthritis, Knee | Active_Not_Recruiting | 2011-07-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT01063751 | Tritanium® Primary Acetabular Shell Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-07-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT03668691 | Clinical Outcomes of Joint Arthroplasty | — | Osteoarthritis, Knee | Active_Not_Recruiting | 2011-07-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT01063751 | Tritanium® Primary Acetabular Shell Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-07-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT01390038 | Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder Arthroplasty | Phase3 | Primary Generalized (Osteo)Arthritis | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT03668691 | Clinical Outcomes of Joint Arthroplasty | — | Osteoarthritis, Knee | Active_Not_Recruiting | 2011-07-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT01390038 | Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder Arthroplasty | Phase3 | Primary Generalized (Osteo)Arthritis | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01063751 | Tritanium® Primary Acetabular Shell Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-07-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT03668691 | Clinical Outcomes of Joint Arthroplasty | — | Osteoarthritis, Knee | Active_Not_Recruiting | 2011-07-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT01063751 | Tritanium® Primary Acetabular Shell Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-07-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT01390038 | Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder Arthroplasty | Phase3 | Primary Generalized (Osteo)Arthritis | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT03668691 | Clinical Outcomes of Joint Arthroplasty | — | Osteoarthritis, Knee | Active_Not_Recruiting | 2011-07-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT01390038 | Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder Arthroplasty | Phase3 | Primary Generalized (Osteo)Arthritis | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01063751 | Tritanium® Primary Acetabular Shell Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-07-01 | 2023-12-30 | ClinicalTrials.gov |
| NCT01420237 | Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-06-01 | 2023-11-09 | ClinicalTrials.gov |
| NCT01420237 | Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-06-01 | 2023-11-09 | ClinicalTrials.gov |
| NCT01420237 | Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-06-01 | 2023-11-09 | ClinicalTrials.gov |
| NCT01420237 | Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-06-01 | 2023-11-09 | ClinicalTrials.gov |
| NCT01420237 | Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-06-01 | 2023-11-09 | ClinicalTrials.gov |
| NCT01420237 | Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study | Na | Arthroplasty, Replacement, Hip | Terminated | 2011-06-01 | 2023-11-09 | ClinicalTrials.gov |
| NCT02444299 | Aequalis Resurfacing Head Study | — | Localized, Primary Osteoarthritis | Unknown | 2011-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02444299 | Aequalis Resurfacing Head Study | — | Localized, Primary Osteoarthritis | Unknown | 2011-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02444299 | Aequalis Resurfacing Head Study | — | Localized, Primary Osteoarthritis | Unknown | 2011-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02444299 | Aequalis Resurfacing Head Study | — | Localized, Primary Osteoarthritis | Unknown | 2011-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02444299 | Aequalis Resurfacing Head Study | — | Localized, Primary Osteoarthritis | Unknown | 2011-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02444299 | Aequalis Resurfacing Head Study | — | Localized, Primary Osteoarthritis | Unknown | 2011-04-01 | 2021-04-01 | ClinicalTrials.gov |
| NCT02424760 | Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interposi… | — | Localized, Primary Osteoarthritis | Unknown | 2011-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02424760 | Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interposi… | — | Localized, Primary Osteoarthritis | Unknown | 2011-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02424760 | Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interposi… | — | Localized, Primary Osteoarthritis | Unknown | 2011-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02424760 | Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interposi… | — | Localized, Primary Osteoarthritis | Unknown | 2011-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02424760 | Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interposi… | — | Localized, Primary Osteoarthritis | Unknown | 2011-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02424760 | Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interposi… | — | Localized, Primary Osteoarthritis | Unknown | 2011-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT01270867 | Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci… | Na | Ischemic Stroke | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01270867 | Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci… | Na | Ischemic Stroke | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01270867 | Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci… | Na | Ischemic Stroke | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01270867 | Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci… | Na | Ischemic Stroke | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01270867 | Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci… | Na | Ischemic Stroke | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01270867 | Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci… | Na | Ischemic Stroke | Completed | 2011-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01641848 | INBONE™ Total Ankle Prosthesis With Long Talar Stem | Na | Arthritis | Terminated | 2010-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01641848 | INBONE™ Total Ankle Prosthesis With Long Talar Stem | Na | Arthritis | Terminated | 2010-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01641848 | INBONE™ Total Ankle Prosthesis With Long Talar Stem | Na | Arthritis | Terminated | 2010-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01641848 | INBONE™ Total Ankle Prosthesis With Long Talar Stem | Na | Arthritis | Terminated | 2010-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01641848 | INBONE™ Total Ankle Prosthesis With Long Talar Stem | Na | Arthritis | Terminated | 2010-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01641848 | INBONE™ Total Ankle Prosthesis With Long Talar Stem | Na | Arthritis | Terminated | 2010-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01257568 | Rejuvenate Modular Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2010-11-01 | 2022-01-20 | ClinicalTrials.gov |
| NCT01257568 | Rejuvenate Modular Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2010-11-01 | 2022-01-20 | ClinicalTrials.gov |
| NCT01257568 | Rejuvenate Modular Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2010-11-01 | 2022-01-20 | ClinicalTrials.gov |
| NCT01257568 | Rejuvenate Modular Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2010-11-01 | 2022-01-20 | ClinicalTrials.gov |
| NCT01257568 | Rejuvenate Modular Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2010-11-01 | 2022-01-20 | ClinicalTrials.gov |
| NCT01257568 | Rejuvenate Modular Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2010-11-01 | 2022-01-20 | ClinicalTrials.gov |
| NCT01366989 | INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation | — | Arthrodesis | Terminated | 2010-10-01 | 2013-06-04 | ClinicalTrials.gov |
| NCT01366989 | INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation | — | Arthrodesis | Terminated | 2010-10-01 | 2013-06-04 | ClinicalTrials.gov |
| NCT01366989 | INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation | — | Arthrodesis | Terminated | 2010-10-01 | 2013-06-04 | ClinicalTrials.gov |
| NCT01366989 | INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation | — | Arthrodesis | Terminated | 2010-10-01 | 2013-06-04 | ClinicalTrials.gov |
| NCT01366989 | INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation | — | Arthrodesis | Terminated | 2010-10-01 | 2013-06-04 | ClinicalTrials.gov |
| NCT01366989 | INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation | — | Arthrodesis | Terminated | 2010-10-01 | 2013-06-04 | ClinicalTrials.gov |
| NCT01248182 | Bone to Skin Thickness Study: Obese Versus Normal Population | — | Fracture | Terminated | 2010-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01248182 | Bone to Skin Thickness Study: Obese Versus Normal Population | — | Fracture | Terminated | 2010-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01248182 | Bone to Skin Thickness Study: Obese Versus Normal Population | — | Fracture | Terminated | 2010-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01248182 | Bone to Skin Thickness Study: Obese Versus Normal Population | — | Fracture | Terminated | 2010-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01248182 | Bone to Skin Thickness Study: Obese Versus Normal Population | — | Fracture | Terminated | 2010-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01248182 | Bone to Skin Thickness Study: Obese Versus Normal Population | — | Fracture | Terminated | 2010-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01353495 | Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Fo… | Na | Diabetic Foot Ulcers | Completed | 2010-04-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01353495 | Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Fo… | Na | Diabetic Foot Ulcers | Completed | 2010-04-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01353495 | Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Fo… | Na | Diabetic Foot Ulcers | Completed | 2010-04-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01353495 | Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Fo… | Na | Diabetic Foot Ulcers | Completed | 2010-04-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01353495 | Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Fo… | Na | Diabetic Foot Ulcers | Completed | 2010-04-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01353495 | Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Fo… | Na | Diabetic Foot Ulcers | Completed | 2010-04-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01088672 | Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Str… | Phase4 | Ischemic Stroke | Completed | 2010-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01088672 | Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Str… | Phase4 | Ischemic Stroke | Completed | 2010-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01088672 | Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Str… | Phase4 | Ischemic Stroke | Completed | 2010-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01088672 | Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Str… | Phase4 | Ischemic Stroke | Completed | 2010-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01088672 | Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Str… | Phase4 | Ischemic Stroke | Completed | 2010-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01088672 | Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Str… | Phase4 | Ischemic Stroke | Completed | 2010-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00966979 | Triathlon® Partial Knee Replacement (PKR) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2010-01-01 | 2023-05-01 | ClinicalTrials.gov |
| NCT00966979 | Triathlon® Partial Knee Replacement (PKR) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2010-01-01 | 2023-05-01 | ClinicalTrials.gov |
| NCT00966979 | Triathlon® Partial Knee Replacement (PKR) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2010-01-01 | 2023-05-01 | ClinicalTrials.gov |
| NCT00966979 | Triathlon® Partial Knee Replacement (PKR) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2010-01-01 | 2023-05-01 | ClinicalTrials.gov |
| NCT00966979 | Triathlon® Partial Knee Replacement (PKR) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2010-01-01 | 2023-05-01 | ClinicalTrials.gov |
| NCT00966979 | Triathlon® Partial Knee Replacement (PKR) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2010-01-01 | 2023-05-01 | ClinicalTrials.gov |
| NCT01041937 | Total Knee Arthroplasty (TKA) Cemented Versus Cementless Tibial Prosthesis Study | Na | Osteoarthritis | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01041937 | Total Knee Arthroplasty (TKA) Cemented Versus Cementless Tibial Prosthesis Study | Na | Osteoarthritis | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01041937 | Total Knee Arthroplasty (TKA) Cemented Versus Cementless Tibial Prosthesis Study | Na | Osteoarthritis | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01041937 | Total Knee Arthroplasty (TKA) Cemented Versus Cementless Tibial Prosthesis Study | Na | Osteoarthritis | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01041937 | Total Knee Arthroplasty (TKA) Cemented Versus Cementless Tibial Prosthesis Study | Na | Osteoarthritis | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01041937 | Total Knee Arthroplasty (TKA) Cemented Versus Cementless Tibial Prosthesis Study | Na | Osteoarthritis | Completed | 2009-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01288586 | Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR … | — | Primary Arthrosis | Completed | 2009-10-05 | 2016-11-14 | ClinicalTrials.gov |
| NCT01288586 | Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR … | — | Primary Arthrosis | Completed | 2009-10-05 | 2016-11-14 | ClinicalTrials.gov |
| NCT01288586 | Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR … | — | Primary Arthrosis | Completed | 2009-10-05 | 2016-11-14 | ClinicalTrials.gov |
| NCT01288586 | Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR … | — | Primary Arthrosis | Completed | 2009-10-05 | 2016-11-14 | ClinicalTrials.gov |
| NCT01288586 | Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR … | — | Primary Arthrosis | Completed | 2009-10-05 | 2016-11-14 | ClinicalTrials.gov |
| NCT01288586 | Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR … | — | Primary Arthrosis | Completed | 2009-10-05 | 2016-11-14 | ClinicalTrials.gov |
| NCT01025037 | Outcomes in Rotator Cuff Repair Using Graft Reinforcement | Na | Rotator Cuff Tear | Completed | 2009-10-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01025037 | Outcomes in Rotator Cuff Repair Using Graft Reinforcement | Na | Rotator Cuff Tear | Completed | 2009-10-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01025037 | Outcomes in Rotator Cuff Repair Using Graft Reinforcement | Na | Rotator Cuff Tear | Completed | 2009-10-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01025037 | Outcomes in Rotator Cuff Repair Using Graft Reinforcement | Na | Rotator Cuff Tear | Completed | 2009-10-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01025037 | Outcomes in Rotator Cuff Repair Using Graft Reinforcement | Na | Rotator Cuff Tear | Completed | 2009-10-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01025037 | Outcomes in Rotator Cuff Repair Using Graft Reinforcement | Na | Rotator Cuff Tear | Completed | 2009-10-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00958789 | Triathlon Total Stabilizer (TS) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2009-07-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT00958789 | Triathlon Total Stabilizer (TS) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2009-07-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT00958789 | Triathlon Total Stabilizer (TS) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2009-07-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT00958789 | Triathlon Total Stabilizer (TS) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2009-07-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT00958789 | Triathlon Total Stabilizer (TS) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2009-07-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT00958789 | Triathlon Total Stabilizer (TS) Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2009-07-01 | 2019-03-28 | ClinicalTrials.gov |
| NCT00937170 | Study Comparing Traditional and Gender-specific Total Knee Replacement Designs | Na | Knee Osteoarthritis | Withdrawn | 2009-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00937170 | Study Comparing Traditional and Gender-specific Total Knee Replacement Designs | Na | Knee Osteoarthritis | Withdrawn | 2009-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00937170 | Study Comparing Traditional and Gender-specific Total Knee Replacement Designs | Na | Knee Osteoarthritis | Withdrawn | 2009-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00937170 | Study Comparing Traditional and Gender-specific Total Knee Replacement Designs | Na | Knee Osteoarthritis | Withdrawn | 2009-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00937170 | Study Comparing Traditional and Gender-specific Total Knee Replacement Designs | Na | Knee Osteoarthritis | Withdrawn | 2009-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00937170 | Study Comparing Traditional and Gender-specific Total Knee Replacement Designs | Na | Knee Osteoarthritis | Withdrawn | 2009-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT02524730 | Scorpio NRG (eNeRGize) Cruciate Retaining (CR) Post-market International Outcom… | Na | Arthroplasty, Replacement, Knee | Completed | 2009-05-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02524730 | Scorpio NRG (eNeRGize) Cruciate Retaining (CR) Post-market International Outcom… | Na | Arthroplasty, Replacement, Knee | Completed | 2009-05-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02524730 | Scorpio NRG (eNeRGize) Cruciate Retaining (CR) Post-market International Outcom… | Na | Arthroplasty, Replacement, Knee | Completed | 2009-05-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02524730 | Scorpio NRG (eNeRGize) Cruciate Retaining (CR) Post-market International Outcom… | Na | Arthroplasty, Replacement, Knee | Completed | 2009-05-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02524730 | Scorpio NRG (eNeRGize) Cruciate Retaining (CR) Post-market International Outcom… | Na | Arthroplasty, Replacement, Knee | Completed | 2009-05-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02524730 | Scorpio NRG (eNeRGize) Cruciate Retaining (CR) Post-market International Outcom… | Na | Arthroplasty, Replacement, Knee | Completed | 2009-05-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT01180582 | Roentgen Stereophotogrammetric Analysis (RSA) and Dual Energy X-ray Absorptiome… | Na | Osteoarthritis, Knee | Completed | 2009-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01180582 | Roentgen Stereophotogrammetric Analysis (RSA) and Dual Energy X-ray Absorptiome… | Na | Osteoarthritis, Knee | Completed | 2009-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01180582 | Roentgen Stereophotogrammetric Analysis (RSA) and Dual Energy X-ray Absorptiome… | Na | Osteoarthritis, Knee | Completed | 2009-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01180582 | Roentgen Stereophotogrammetric Analysis (RSA) and Dual Energy X-ray Absorptiome… | Na | Osteoarthritis, Knee | Completed | 2009-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01180582 | Roentgen Stereophotogrammetric Analysis (RSA) and Dual Energy X-ray Absorptiome… | Na | Osteoarthritis, Knee | Completed | 2009-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01180582 | Roentgen Stereophotogrammetric Analysis (RSA) and Dual Energy X-ray Absorptiome… | Na | Osteoarthritis, Knee | Completed | 2009-04-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT00949897 | Comparison Study of Biofoam Porous Metal Versus Allograft to Treat Adult Acquir… | Phase4 | Adult Acquired Flatfoot | Withdrawn | 2009-03-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00949897 | Comparison Study of Biofoam Porous Metal Versus Allograft to Treat Adult Acquir… | Phase4 | Adult Acquired Flatfoot | Withdrawn | 2009-03-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00949897 | Comparison Study of Biofoam Porous Metal Versus Allograft to Treat Adult Acquir… | Phase4 | Adult Acquired Flatfoot | Withdrawn | 2009-03-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00949897 | Comparison Study of Biofoam Porous Metal Versus Allograft to Treat Adult Acquir… | Phase4 | Adult Acquired Flatfoot | Withdrawn | 2009-03-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00949897 | Comparison Study of Biofoam Porous Metal Versus Allograft to Treat Adult Acquir… | Phase4 | Adult Acquired Flatfoot | Withdrawn | 2009-03-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00949897 | Comparison Study of Biofoam Porous Metal Versus Allograft to Treat Adult Acquir… | Phase4 | Adult Acquired Flatfoot | Withdrawn | 2009-03-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00829803 | A Study to Assess Indices of SNAP vs VISTA on Surgical Patients Undergoing Gene… | Na | Anesthesia, General | Completed | 2009-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00929383 | An International Registry of the Wingspan™ Stent System for the Treatment of In… | — | Intracranial Atherosclerosis | Completed | 2009-02-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829803 | A Study to Assess Indices of SNAP vs VISTA on Surgical Patients Undergoing Gene… | Na | Anesthesia, General | Completed | 2009-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00929383 | An International Registry of the Wingspan™ Stent System for the Treatment of In… | — | Intracranial Atherosclerosis | Completed | 2009-02-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00929383 | An International Registry of the Wingspan™ Stent System for the Treatment of In… | — | Intracranial Atherosclerosis | Completed | 2009-02-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829803 | A Study to Assess Indices of SNAP vs VISTA on Surgical Patients Undergoing Gene… | Na | Anesthesia, General | Completed | 2009-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00929383 | An International Registry of the Wingspan™ Stent System for the Treatment of In… | — | Intracranial Atherosclerosis | Completed | 2009-02-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829803 | A Study to Assess Indices of SNAP vs VISTA on Surgical Patients Undergoing Gene… | Na | Anesthesia, General | Completed | 2009-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00929383 | An International Registry of the Wingspan™ Stent System for the Treatment of In… | — | Intracranial Atherosclerosis | Completed | 2009-02-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00829803 | A Study to Assess Indices of SNAP vs VISTA on Surgical Patients Undergoing Gene… | Na | Anesthesia, General | Completed | 2009-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00829803 | A Study to Assess Indices of SNAP vs VISTA on Surgical Patients Undergoing Gene… | Na | Anesthesia, General | Completed | 2009-02-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00929383 | An International Registry of the Wingspan™ Stent System for the Treatment of In… | — | Intracranial Atherosclerosis | Completed | 2009-02-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT03509480 | Vitoss With Bone Marrow Aspirate Versus Prodense | Na | Bone Lesion | Completed | 2009-01-01 | 2018-02-28 | ClinicalTrials.gov |
| NCT03509480 | Vitoss With Bone Marrow Aspirate Versus Prodense | Na | Bone Lesion | Completed | 2009-01-01 | 2018-02-28 | ClinicalTrials.gov |
| NCT03509480 | Vitoss With Bone Marrow Aspirate Versus Prodense | Na | Bone Lesion | Completed | 2009-01-01 | 2018-02-28 | ClinicalTrials.gov |
| NCT03509480 | Vitoss With Bone Marrow Aspirate Versus Prodense | Na | Bone Lesion | Completed | 2009-01-01 | 2018-02-28 | ClinicalTrials.gov |
| NCT03509480 | Vitoss With Bone Marrow Aspirate Versus Prodense | Na | Bone Lesion | Completed | 2009-01-01 | 2018-02-28 | ClinicalTrials.gov |
| NCT03509480 | Vitoss With Bone Marrow Aspirate Versus Prodense | Na | Bone Lesion | Completed | 2009-01-01 | 2018-02-28 | ClinicalTrials.gov |
| NCT00928265 | Safety and Efficacy of Neuroform3TM for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2008-07-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00928265 | Safety and Efficacy of Neuroform3TM for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2008-07-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00928265 | Safety and Efficacy of Neuroform3TM for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2008-07-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00928265 | Safety and Efficacy of Neuroform3TM for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2008-07-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00928265 | Safety and Efficacy of Neuroform3TM for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2008-07-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00928265 | Safety and Efficacy of Neuroform3TM for Intracranial Aneurysm Treatment | — | Intracranial Aneurysm | Completed | 2008-07-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00654615 | Fixation of Unstable Distal Radius Fractures | Na | Distal Radius Fractures | Completed | 2008-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00654615 | Fixation of Unstable Distal Radius Fractures | Na | Distal Radius Fractures | Completed | 2008-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00654615 | Fixation of Unstable Distal Radius Fractures | Na | Distal Radius Fractures | Completed | 2008-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00654615 | Fixation of Unstable Distal Radius Fractures | Na | Distal Radius Fractures | Completed | 2008-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00654615 | Fixation of Unstable Distal Radius Fractures | Na | Distal Radius Fractures | Completed | 2008-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00654615 | Fixation of Unstable Distal Radius Fractures | Na | Distal Radius Fractures | Completed | 2008-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT00657956 | Roentgen Stereophotogrammetric Analysis (RSA) to Evaluate Fixation of Biofoam A… | Na | Osteoarthritis | Completed | 2008-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00657956 | Roentgen Stereophotogrammetric Analysis (RSA) to Evaluate Fixation of Biofoam A… | Na | Osteoarthritis | Completed | 2008-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00657956 | Roentgen Stereophotogrammetric Analysis (RSA) to Evaluate Fixation of Biofoam A… | Na | Osteoarthritis | Completed | 2008-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00657956 | Roentgen Stereophotogrammetric Analysis (RSA) to Evaluate Fixation of Biofoam A… | Na | Osteoarthritis | Completed | 2008-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00657956 | Roentgen Stereophotogrammetric Analysis (RSA) to Evaluate Fixation of Biofoam A… | Na | Osteoarthritis | Completed | 2008-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00657956 | Roentgen Stereophotogrammetric Analysis (RSA) to Evaluate Fixation of Biofoam A… | Na | Osteoarthritis | Completed | 2008-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00478478 | Merci Registry - Real World Use of the Merci Retrieval System in Acute Ischemic… | — | Ischemic Stroke | Completed | 2007-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01326156 | Study of Knee Replacements for Patellofemoral Osteoarthritis | Na | Osteoarthritis, Knee | Active_Not_Recruiting | 2007-06-01 | 2040-10-01 | ClinicalTrials.gov |
| NCT01326156 | Study of Knee Replacements for Patellofemoral Osteoarthritis | Na | Osteoarthritis, Knee | Active_Not_Recruiting | 2007-06-01 | 2040-10-01 | ClinicalTrials.gov |
| NCT00478478 | Merci Registry - Real World Use of the Merci Retrieval System in Acute Ischemic… | — | Ischemic Stroke | Completed | 2007-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01326156 | Study of Knee Replacements for Patellofemoral Osteoarthritis | Na | Osteoarthritis, Knee | Active_Not_Recruiting | 2007-06-01 | 2040-10-01 | ClinicalTrials.gov |
| NCT00478478 | Merci Registry - Real World Use of the Merci Retrieval System in Acute Ischemic… | — | Ischemic Stroke | Completed | 2007-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01326156 | Study of Knee Replacements for Patellofemoral Osteoarthritis | Na | Osteoarthritis, Knee | Active_Not_Recruiting | 2007-06-01 | 2040-10-01 | ClinicalTrials.gov |
| NCT00478478 | Merci Registry - Real World Use of the Merci Retrieval System in Acute Ischemic… | — | Ischemic Stroke | Completed | 2007-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00478478 | Merci Registry - Real World Use of the Merci Retrieval System in Acute Ischemic… | — | Ischemic Stroke | Completed | 2007-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00478478 | Merci Registry - Real World Use of the Merci Retrieval System in Acute Ischemic… | — | Ischemic Stroke | Completed | 2007-06-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01326156 | Study of Knee Replacements for Patellofemoral Osteoarthritis | Na | Osteoarthritis, Knee | Active_Not_Recruiting | 2007-06-01 | 2040-10-01 | ClinicalTrials.gov |
| NCT01326156 | Study of Knee Replacements for Patellofemoral Osteoarthritis | Na | Osteoarthritis, Knee | Active_Not_Recruiting | 2007-06-01 | 2040-10-01 | ClinicalTrials.gov |
| NCT00555945 | Re-Evaluation of GAmma3 Intramedullary Nails in Hip Fracture (REGAIN) | Na | Femoral Neck Fractures | Completed | 2007-05-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01218035 | Efficacy of Zoledronic Acid in Enhancement of Early Stability of Cementless Pri… | Phase4 | Hip Osteoarthritis | Completed | 2007-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00555945 | Re-Evaluation of GAmma3 Intramedullary Nails in Hip Fracture (REGAIN) | Na | Femoral Neck Fractures | Completed | 2007-05-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01218035 | Efficacy of Zoledronic Acid in Enhancement of Early Stability of Cementless Pri… | Phase4 | Hip Osteoarthritis | Completed | 2007-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00555945 | Re-Evaluation of GAmma3 Intramedullary Nails in Hip Fracture (REGAIN) | Na | Femoral Neck Fractures | Completed | 2007-05-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01218035 | Efficacy of Zoledronic Acid in Enhancement of Early Stability of Cementless Pri… | Phase4 | Hip Osteoarthritis | Completed | 2007-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00555945 | Re-Evaluation of GAmma3 Intramedullary Nails in Hip Fracture (REGAIN) | Na | Femoral Neck Fractures | Completed | 2007-05-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00555945 | Re-Evaluation of GAmma3 Intramedullary Nails in Hip Fracture (REGAIN) | Na | Femoral Neck Fractures | Completed | 2007-05-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00555945 | Re-Evaluation of GAmma3 Intramedullary Nails in Hip Fracture (REGAIN) | Na | Femoral Neck Fractures | Completed | 2007-05-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01218035 | Efficacy of Zoledronic Acid in Enhancement of Early Stability of Cementless Pri… | Phase4 | Hip Osteoarthritis | Completed | 2007-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01218035 | Efficacy of Zoledronic Acid in Enhancement of Early Stability of Cementless Pri… | Phase4 | Hip Osteoarthritis | Completed | 2007-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01218035 | Efficacy of Zoledronic Acid in Enhancement of Early Stability of Cementless Pri… | Phase4 | Hip Osteoarthritis | Completed | 2007-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT00510458 | LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2007-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00456781 | Use of Graft Jacket for Rotator Cuff Repair | Na | Rotator Cuff Tear | Completed | 2007-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00456781 | Use of Graft Jacket for Rotator Cuff Repair | Na | Rotator Cuff Tear | Completed | 2007-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00510458 | LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2007-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00510458 | LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2007-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00510458 | LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2007-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00510458 | LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2007-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00456781 | Use of Graft Jacket for Rotator Cuff Repair | Na | Rotator Cuff Tear | Completed | 2007-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00456781 | Use of Graft Jacket for Rotator Cuff Repair | Na | Rotator Cuff Tear | Completed | 2007-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00419276 | Effect of Ambulatory Continuous Femoral Nerve Blocks on Readiness-for-Discharge… | Na | Total Knee Arthroplasty | Completed | 2007-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00419276 | Effect of Ambulatory Continuous Femoral Nerve Blocks on Readiness-for-Discharge… | Na | Total Knee Arthroplasty | Completed | 2007-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00419276 | Effect of Ambulatory Continuous Femoral Nerve Blocks on Readiness-for-Discharge… | Na | Total Knee Arthroplasty | Completed | 2007-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00419276 | Effect of Ambulatory Continuous Femoral Nerve Blocks on Readiness-for-Discharge… | Na | Total Knee Arthroplasty | Completed | 2007-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00456781 | Use of Graft Jacket for Rotator Cuff Repair | Na | Rotator Cuff Tear | Completed | 2007-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00456781 | Use of Graft Jacket for Rotator Cuff Repair | Na | Rotator Cuff Tear | Completed | 2007-04-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00510458 | LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2007-04-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00419276 | Effect of Ambulatory Continuous Femoral Nerve Blocks on Readiness-for-Discharge… | Na | Total Knee Arthroplasty | Completed | 2007-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00419276 | Effect of Ambulatory Continuous Femoral Nerve Blocks on Readiness-for-Discharge… | Na | Total Knee Arthroplasty | Completed | 2007-04-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00396981 | MAPS Trial: Matrix And Platinum Science | Phase4 | Intracranial Aneurysms | Completed | 2007-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00396981 | MAPS Trial: Matrix And Platinum Science | Phase4 | Intracranial Aneurysms | Completed | 2007-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00396981 | MAPS Trial: Matrix And Platinum Science | Phase4 | Intracranial Aneurysms | Completed | 2007-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00396981 | MAPS Trial: Matrix And Platinum Science | Phase4 | Intracranial Aneurysms | Completed | 2007-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00396981 | MAPS Trial: Matrix And Platinum Science | Phase4 | Intracranial Aneurysms | Completed | 2007-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT00396981 | MAPS Trial: Matrix And Platinum Science | Phase4 | Intracranial Aneurysms | Completed | 2007-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02522728 | Evaluation of Triathlon - A New Total Knee Prosthesis System - Roentgen Stereop… | Na | Arthroplasty, Replacement, Knee | Completed | 2007-01-23 | 2017-09-14 | ClinicalTrials.gov |
| NCT02522728 | Evaluation of Triathlon - A New Total Knee Prosthesis System - Roentgen Stereop… | Na | Arthroplasty, Replacement, Knee | Completed | 2007-01-23 | 2017-09-14 | ClinicalTrials.gov |
| NCT02522728 | Evaluation of Triathlon - A New Total Knee Prosthesis System - Roentgen Stereop… | Na | Arthroplasty, Replacement, Knee | Completed | 2007-01-23 | 2017-09-14 | ClinicalTrials.gov |
| NCT02522728 | Evaluation of Triathlon - A New Total Knee Prosthesis System - Roentgen Stereop… | Na | Arthroplasty, Replacement, Knee | Completed | 2007-01-23 | 2017-09-14 | ClinicalTrials.gov |
| NCT02522728 | Evaluation of Triathlon - A New Total Knee Prosthesis System - Roentgen Stereop… | Na | Arthroplasty, Replacement, Knee | Completed | 2007-01-23 | 2017-09-14 | ClinicalTrials.gov |
| NCT02522728 | Evaluation of Triathlon - A New Total Knee Prosthesis System - Roentgen Stereop… | Na | Arthroplasty, Replacement, Knee | Completed | 2007-01-23 | 2017-09-14 | ClinicalTrials.gov |
| NCT00409266 | CT Assessment of Minimally Invasive Surgery and Computer Assisted Navigation in… | Na | Total Knee Arthroplasty | Withdrawn | 2007-01-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00409266 | CT Assessment of Minimally Invasive Surgery and Computer Assisted Navigation in… | Na | Total Knee Arthroplasty | Withdrawn | 2007-01-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT02491424 | Intraosseous Transcutaneous Amputation Prosthesis | Na | Traumatic Amputation of Lower Extremity | Completed | 2007-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00409266 | CT Assessment of Minimally Invasive Surgery and Computer Assisted Navigation in… | Na | Total Knee Arthroplasty | Withdrawn | 2007-01-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT02491424 | Intraosseous Transcutaneous Amputation Prosthesis | Na | Traumatic Amputation of Lower Extremity | Completed | 2007-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02491424 | Intraosseous Transcutaneous Amputation Prosthesis | Na | Traumatic Amputation of Lower Extremity | Completed | 2007-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00409266 | CT Assessment of Minimally Invasive Surgery and Computer Assisted Navigation in… | Na | Total Knee Arthroplasty | Withdrawn | 2007-01-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT02491424 | Intraosseous Transcutaneous Amputation Prosthesis | Na | Traumatic Amputation of Lower Extremity | Completed | 2007-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00409266 | CT Assessment of Minimally Invasive Surgery and Computer Assisted Navigation in… | Na | Total Knee Arthroplasty | Withdrawn | 2007-01-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT02491424 | Intraosseous Transcutaneous Amputation Prosthesis | Na | Traumatic Amputation of Lower Extremity | Completed | 2007-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02491424 | Intraosseous Transcutaneous Amputation Prosthesis | Na | Traumatic Amputation of Lower Extremity | Completed | 2007-01-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00409266 | CT Assessment of Minimally Invasive Surgery and Computer Assisted Navigation in… | Na | Total Knee Arthroplasty | Withdrawn | 2007-01-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00427752 | Abdominal Exploration Without Incisions | Early_Phase1 | Pancreatic Cancer | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01135030 | Anterior Referencing Versus Posterior Referencing in Minimally Invasive Total K… | Na | Osteoarthritis | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00427752 | Abdominal Exploration Without Incisions | Early_Phase1 | Pancreatic Cancer | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01135030 | Anterior Referencing Versus Posterior Referencing in Minimally Invasive Total K… | Na | Osteoarthritis | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00427752 | Abdominal Exploration Without Incisions | Early_Phase1 | Pancreatic Cancer | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT02535741 | Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee | Na | Total Knee Arthroplasty | Completed | 2006-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02535741 | Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee | Na | Total Knee Arthroplasty | Completed | 2006-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02535741 | Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee | Na | Total Knee Arthroplasty | Completed | 2006-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01135030 | Anterior Referencing Versus Posterior Referencing in Minimally Invasive Total K… | Na | Osteoarthritis | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00427752 | Abdominal Exploration Without Incisions | Early_Phase1 | Pancreatic Cancer | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00427752 | Abdominal Exploration Without Incisions | Early_Phase1 | Pancreatic Cancer | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01135030 | Anterior Referencing Versus Posterior Referencing in Minimally Invasive Total K… | Na | Osteoarthritis | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT02535741 | Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee | Na | Total Knee Arthroplasty | Completed | 2006-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02535741 | Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee | Na | Total Knee Arthroplasty | Completed | 2006-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01135030 | Anterior Referencing Versus Posterior Referencing in Minimally Invasive Total K… | Na | Osteoarthritis | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT02535741 | Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee | Na | Total Knee Arthroplasty | Completed | 2006-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT00427752 | Abdominal Exploration Without Incisions | Early_Phase1 | Pancreatic Cancer | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01135030 | Anterior Referencing Versus Posterior Referencing in Minimally Invasive Total K… | Na | Osteoarthritis | Completed | 2006-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00380549 | A Comparison of an Advanced Metal Hip System to a Resurfacing Hip System | Na | Osteoarthritis | Completed | 2006-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00380549 | A Comparison of an Advanced Metal Hip System to a Resurfacing Hip System | Na | Osteoarthritis | Completed | 2006-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00380549 | A Comparison of an Advanced Metal Hip System to a Resurfacing Hip System | Na | Osteoarthritis | Completed | 2006-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00380549 | A Comparison of an Advanced Metal Hip System to a Resurfacing Hip System | Na | Osteoarthritis | Completed | 2006-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00380549 | A Comparison of an Advanced Metal Hip System to a Resurfacing Hip System | Na | Osteoarthritis | Completed | 2006-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00380549 | A Comparison of an Advanced Metal Hip System to a Resurfacing Hip System | Na | Osteoarthritis | Completed | 2006-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00957658 | Accolade® TMZF® Hip Stem Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2006-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00957658 | Accolade® TMZF® Hip Stem Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2006-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00957658 | Accolade® TMZF® Hip Stem Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2006-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00957658 | Accolade® TMZF® Hip Stem Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2006-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00957658 | Accolade® TMZF® Hip Stem Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2006-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00957658 | Accolade® TMZF® Hip Stem Outcomes Study | Na | Arthroplasty, Replacement, Hip | Completed | 2006-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00436982 | Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. Du… | Na | Arthroplasty, Replacement, Knee | Completed | 2006-02-01 | 2017-01-04 | ClinicalTrials.gov |
| NCT00436982 | Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. Du… | Na | Arthroplasty, Replacement, Knee | Completed | 2006-02-01 | 2017-01-04 | ClinicalTrials.gov |
| NCT00436982 | Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. Du… | Na | Arthroplasty, Replacement, Knee | Completed | 2006-02-01 | 2017-01-04 | ClinicalTrials.gov |
| NCT00436982 | Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. Du… | Na | Arthroplasty, Replacement, Knee | Completed | 2006-02-01 | 2017-01-04 | ClinicalTrials.gov |
| NCT00436982 | Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. Du… | Na | Arthroplasty, Replacement, Knee | Completed | 2006-02-01 | 2017-01-04 | ClinicalTrials.gov |
| NCT00436982 | Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. Du… | Na | Arthroplasty, Replacement, Knee | Completed | 2006-02-01 | 2017-01-04 | ClinicalTrials.gov |
| NCT00586976 | A Phase II/III Study of Continuous Local Anesthetic Infusion in Median Sternoto… | Phase2 | Cardiac Surgery | Terminated | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00586976 | A Phase II/III Study of Continuous Local Anesthetic Infusion in Median Sternoto… | Phase2 | Cardiac Surgery | Terminated | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01133249 | Total Hip Registry | — | Osteoarthritis | Unknown | 2005-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01133249 | Total Hip Registry | — | Osteoarthritis | Unknown | 2005-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT00586976 | A Phase II/III Study of Continuous Local Anesthetic Infusion in Median Sternoto… | Phase2 | Cardiac Surgery | Terminated | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01133249 | Total Hip Registry | — | Osteoarthritis | Unknown | 2005-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01133249 | Total Hip Registry | — | Osteoarthritis | Unknown | 2005-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT00586976 | A Phase II/III Study of Continuous Local Anesthetic Infusion in Median Sternoto… | Phase2 | Cardiac Surgery | Terminated | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00586976 | A Phase II/III Study of Continuous Local Anesthetic Infusion in Median Sternoto… | Phase2 | Cardiac Surgery | Terminated | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00586976 | A Phase II/III Study of Continuous Local Anesthetic Infusion in Median Sternoto… | Phase2 | Cardiac Surgery | Terminated | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01133249 | Total Hip Registry | — | Osteoarthritis | Unknown | 2005-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01133249 | Total Hip Registry | — | Osteoarthritis | Unknown | 2005-07-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT00958191 | Trident® X3 Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2005-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00958191 | Trident® X3 Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2005-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00958191 | Trident® X3 Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2005-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00958191 | Trident® X3 Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2005-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00958191 | Trident® X3 Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2005-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT00958191 | Trident® X3 Polyethylene Insert Study | Na | Arthroplasty, Replacement, Hip | Completed | 2005-05-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01132365 | Knee Arthroplasty Registry | — | Osteoarthritis, Knee | Unknown | 2005-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01132365 | Knee Arthroplasty Registry | — | Osteoarthritis, Knee | Unknown | 2005-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01132365 | Knee Arthroplasty Registry | — | Osteoarthritis, Knee | Unknown | 2005-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01132365 | Knee Arthroplasty Registry | — | Osteoarthritis, Knee | Unknown | 2005-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01132365 | Knee Arthroplasty Registry | — | Osteoarthritis, Knee | Unknown | 2005-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT01132365 | Knee Arthroplasty Registry | — | Osteoarthritis, Knee | Unknown | 2005-04-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT00957723 | Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2005-02-01 | 2017-09-26 | ClinicalTrials.gov |
| NCT00957723 | Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2005-02-01 | 2017-09-26 | ClinicalTrials.gov |
| NCT00957723 | Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2005-02-01 | 2017-09-26 | ClinicalTrials.gov |
| NCT00957723 | Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2005-02-01 | 2017-09-26 | ClinicalTrials.gov |
| NCT00957723 | Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2005-02-01 | 2017-09-26 | ClinicalTrials.gov |
| NCT00957723 | Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study | Na | Arthroplasty, Replacement, Knee | Completed | 2005-02-01 | 2017-09-26 | ClinicalTrials.gov |
| NCT00135889 | Continuous Femoral Nerve Block Following Total Knee Replacement | Na | Pain | Completed | 2005-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00135889 | Continuous Femoral Nerve Block Following Total Knee Replacement | Na | Pain | Completed | 2005-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00135889 | Continuous Femoral Nerve Block Following Total Knee Replacement | Na | Pain | Completed | 2005-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00135889 | Continuous Femoral Nerve Block Following Total Knee Replacement | Na | Pain | Completed | 2005-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00135889 | Continuous Femoral Nerve Block Following Total Knee Replacement | Na | Pain | Completed | 2005-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00135889 | Continuous Femoral Nerve Block Following Total Knee Replacement | Na | Pain | Completed | 2005-01-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT03469687 | Symax International Study | Na | Hip Osteoarthritis | Completed | 2004-11-02 | 2010-10-11 | ClinicalTrials.gov |
| NCT03469687 | Symax International Study | Na | Hip Osteoarthritis | Completed | 2004-11-02 | 2010-10-11 | ClinicalTrials.gov |
| NCT03469687 | Symax International Study | Na | Hip Osteoarthritis | Completed | 2004-11-02 | 2010-10-11 | ClinicalTrials.gov |
| NCT03469687 | Symax International Study | Na | Hip Osteoarthritis | Completed | 2004-11-02 | 2010-10-11 | ClinicalTrials.gov |
| NCT03469687 | Symax International Study | Na | Hip Osteoarthritis | Completed | 2004-11-02 | 2010-10-11 | ClinicalTrials.gov |
| NCT03469687 | Symax International Study | Na | Hip Osteoarthritis | Completed | 2004-11-02 | 2010-10-11 | ClinicalTrials.gov |
| NCT00962013 | Restoration® Modular Revision Hip System Post Market Study | Na | Arthroplasty, Replacement, Hip | Completed | 2004-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00318071 | Multi MERCI (Mechanical Embolus Removal in Cerebral Ischemia [MERCI™]) | Na | Ischemic Stroke | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00318071 | Multi MERCI (Mechanical Embolus Removal in Cerebral Ischemia [MERCI™]) | Na | Ischemic Stroke | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00318071 | Multi MERCI (Mechanical Embolus Removal in Cerebral Ischemia [MERCI™]) | Na | Ischemic Stroke | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00318071 | Multi MERCI (Mechanical Embolus Removal in Cerebral Ischemia [MERCI™]) | Na | Ischemic Stroke | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00962013 | Restoration® Modular Revision Hip System Post Market Study | Na | Arthroplasty, Replacement, Hip | Completed | 2004-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00962013 | Restoration® Modular Revision Hip System Post Market Study | Na | Arthroplasty, Replacement, Hip | Completed | 2004-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00318071 | Multi MERCI (Mechanical Embolus Removal in Cerebral Ischemia [MERCI™]) | Na | Ischemic Stroke | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00962013 | Restoration® Modular Revision Hip System Post Market Study | Na | Arthroplasty, Replacement, Hip | Completed | 2004-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00962013 | Restoration® Modular Revision Hip System Post Market Study | Na | Arthroplasty, Replacement, Hip | Completed | 2004-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00318071 | Multi MERCI (Mechanical Embolus Removal in Cerebral Ischemia [MERCI™]) | Na | Ischemic Stroke | Completed | 2004-01-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00962013 | Restoration® Modular Revision Hip System Post Market Study | Na | Arthroplasty, Replacement, Hip | Completed | 2004-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02892838 | Should my New Knee Rotate? | Phase4 | Arthritis of the Knee Joint | Completed | 2003-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02892838 | Should my New Knee Rotate? | Phase4 | Arthritis of the Knee Joint | Completed | 2003-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02892838 | Should my New Knee Rotate? | Phase4 | Arthritis of the Knee Joint | Completed | 2003-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02892838 | Should my New Knee Rotate? | Phase4 | Arthritis of the Knee Joint | Completed | 2003-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02892838 | Should my New Knee Rotate? | Phase4 | Arthritis of the Knee Joint | Completed | 2003-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT02892838 | Should my New Knee Rotate? | Phase4 | Arthritis of the Knee Joint | Completed | 2003-09-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00253877 | A Comparison of a Resurfacing Hip System to Standard Total Hip Arthroplasty | Na | Osteoarthritis | Completed | 2003-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00253877 | A Comparison of a Resurfacing Hip System to Standard Total Hip Arthroplasty | Na | Osteoarthritis | Completed | 2003-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00253877 | A Comparison of a Resurfacing Hip System to Standard Total Hip Arthroplasty | Na | Osteoarthritis | Completed | 2003-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00253877 | A Comparison of a Resurfacing Hip System to Standard Total Hip Arthroplasty | Na | Osteoarthritis | Completed | 2003-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00253877 | A Comparison of a Resurfacing Hip System to Standard Total Hip Arthroplasty | Na | Osteoarthritis | Completed | 2003-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00253877 | A Comparison of a Resurfacing Hip System to Standard Total Hip Arthroplasty | Na | Osteoarthritis | Completed | 2003-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01695213 | RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hi… | Phase4 | Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis | Completed | 2003-04-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01695213 | RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hi… | Phase4 | Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis | Completed | 2003-04-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01695213 | RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hi… | Phase4 | Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis | Completed | 2003-04-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01695213 | RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hi… | Phase4 | Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis | Completed | 2003-04-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01695213 | RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hi… | Phase4 | Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis | Completed | 2003-04-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01695213 | RCT Comparing the DEXA Results of the HA-Omnifit Versus the Symax Uncemented Hi… | Phase4 | Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis | Completed | 2003-04-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00960206 | ABC/Trident® Ceramic Post Approval Study | Na | Arthroplasty, Replacement, Hip | Completed | 2003-03-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00960206 | ABC/Trident® Ceramic Post Approval Study | Na | Arthroplasty, Replacement, Hip | Completed | 2003-03-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00960206 | ABC/Trident® Ceramic Post Approval Study | Na | Arthroplasty, Replacement, Hip | Completed | 2003-03-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00960206 | ABC/Trident® Ceramic Post Approval Study | Na | Arthroplasty, Replacement, Hip | Completed | 2003-03-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00960206 | ABC/Trident® Ceramic Post Approval Study | Na | Arthroplasty, Replacement, Hip | Completed | 2003-03-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00960206 | ABC/Trident® Ceramic Post Approval Study | Na | Arthroplasty, Replacement, Hip | Completed | 2003-03-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00253838 | A Comparison of Two Type of Stems in Revision Hip Arthroplasty | Na | Hip Arthroplasty | Completed | 2001-10-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00253838 | A Comparison of Two Type of Stems in Revision Hip Arthroplasty | Na | Hip Arthroplasty | Completed | 2001-10-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00253838 | A Comparison of Two Type of Stems in Revision Hip Arthroplasty | Na | Hip Arthroplasty | Completed | 2001-10-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00253838 | A Comparison of Two Type of Stems in Revision Hip Arthroplasty | Na | Hip Arthroplasty | Completed | 2001-10-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00253838 | A Comparison of Two Type of Stems in Revision Hip Arthroplasty | Na | Hip Arthroplasty | Completed | 2001-10-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00253838 | A Comparison of Two Type of Stems in Revision Hip Arthroplasty | Na | Hip Arthroplasty | Completed | 2001-10-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00405470 | A Prospective Randomized Trial Using Roentgen Stereophotogrammetric Analysis of… | Na | Osteoarthritis, Knee | Completed | 2001-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00405470 | A Prospective Randomized Trial Using Roentgen Stereophotogrammetric Analysis of… | Na | Osteoarthritis, Knee | Completed | 2001-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00405470 | A Prospective Randomized Trial Using Roentgen Stereophotogrammetric Analysis of… | Na | Osteoarthritis, Knee | Completed | 2001-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00405470 | A Prospective Randomized Trial Using Roentgen Stereophotogrammetric Analysis of… | Na | Osteoarthritis, Knee | Completed | 2001-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00405470 | A Prospective Randomized Trial Using Roentgen Stereophotogrammetric Analysis of… | Na | Osteoarthritis, Knee | Completed | 2001-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00405470 | A Prospective Randomized Trial Using Roentgen Stereophotogrammetric Analysis of… | Na | Osteoarthritis, Knee | Completed | 2001-07-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00965146 | Scorpio® Cruciate Retaining (CR) Outcomes Study | Na | Arthropathy of Knee | Terminated | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00965146 | Scorpio® Cruciate Retaining (CR) Outcomes Study | Na | Arthropathy of Knee | Terminated | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00965146 | Scorpio® Cruciate Retaining (CR) Outcomes Study | Na | Arthropathy of Knee | Terminated | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00965146 | Scorpio® Cruciate Retaining (CR) Outcomes Study | Na | Arthropathy of Knee | Terminated | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00965146 | Scorpio® Cruciate Retaining (CR) Outcomes Study | Na | Arthropathy of Knee | Terminated | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00965146 | Scorpio® Cruciate Retaining (CR) Outcomes Study | Na | Arthropathy of Knee | Terminated | 2001-06-01 | — | ClinicalTrials.gov |
| NCT00463424 | Comparison of NeuFlex and Swanson Metacarpophalangeal Implants for Rheumatoid A… | Phase2 | Arthritis, Rheumatoid | Completed | 2000-10-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00463424 | Comparison of NeuFlex and Swanson Metacarpophalangeal Implants for Rheumatoid A… | Phase2 | Arthritis, Rheumatoid | Completed | 2000-10-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00463424 | Comparison of NeuFlex and Swanson Metacarpophalangeal Implants for Rheumatoid A… | Phase2 | Arthritis, Rheumatoid | Completed | 2000-10-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00463424 | Comparison of NeuFlex and Swanson Metacarpophalangeal Implants for Rheumatoid A… | Phase2 | Arthritis, Rheumatoid | Completed | 2000-10-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00463424 | Comparison of NeuFlex and Swanson Metacarpophalangeal Implants for Rheumatoid A… | Phase2 | Arthritis, Rheumatoid | Completed | 2000-10-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00463424 | Comparison of NeuFlex and Swanson Metacarpophalangeal Implants for Rheumatoid A… | Phase2 | Arthritis, Rheumatoid | Completed | 2000-10-01 | 2005-08-01 | ClinicalTrials.gov |
| NCT00958347 | Omnifit Hydroxylapatite (HA) Hip Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 1987-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00958347 | Omnifit Hydroxylapatite (HA) Hip Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 1987-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00958347 | Omnifit Hydroxylapatite (HA) Hip Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 1987-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00958347 | Omnifit Hydroxylapatite (HA) Hip Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 1987-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00958347 | Omnifit Hydroxylapatite (HA) Hip Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 1987-10-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00958347 | Omnifit Hydroxylapatite (HA) Hip Outcomes Study | Na | Arthroplasty, Replacement, Hip | Terminated | 1987-10-01 | 2011-05-01 | ClinicalTrials.gov |
Total clinical trials: 1122
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System | Other | Preclinical | Femoral Fracture | COMPLETED | NCT04015128 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Trident II Tritanium Acetabular Shell | Other | Approved | Arthroplasty, Replacement, Hip | ACTIVE_NOT_RECRUITING | NCT02999009 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Basivertebral nerve ablation | Other | Preclinical | Verteborgenic Low Back Pain | RECRUITING | NCT07392333 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Mako Robotic-Arm Assisted Arthroplasty | Other | Preclinical | Arthropathy of Knee | NOT_YET_RECRUITING | NCT07647354 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Triathlon Tritanium Cone Augments | Other | Approved | Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02521103 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | WITHDRAWN | NCT05591859 |
| Swanson metacarpophalangeal implant | Other | Phase PHASE2 | Arthritis, Rheumatoid | COMPLETED | NCT00463424 |
| NeuFlex metacarpophalangeal implant | Other | Phase PHASE2 | Arthritis, Rheumatoid | COMPLETED | NCT00463424 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Femoral perineural infusion | Other | Approved | Pain | COMPLETED | NCT00135889 |
| Advance Medial Pivot Knee Arthroplasty | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT00405470 |
| Stryker Triathlon Implant (Total knee replacement) | Other | Approved | Knee Osteoarthritis | WITHDRAWN | NCT00937170 |
| Zimmer High Flex LPS Implant (Total knee replacement) | Other | Approved | Knee Osteoarthritis | WITHDRAWN | NCT00937170 |
| Zimmer LPS flex Gender Specific Implant (Total knee replacement) | Other | Approved | Knee Osteoarthritis | WITHDRAWN | NCT00937170 |
| Stryker Triathlon Implant (Total knee replacement) | Other | Approved | Knee Osteoarthritis | WITHDRAWN | NCT00937170 |
| Zimmer High Flex LPS Implant (Total knee replacement) | Other | Approved | Knee Osteoarthritis | WITHDRAWN | NCT00937170 |
| Zimmer LPS flex Gender Specific Implant (Total knee replacement) | Other | Approved | Knee Osteoarthritis | WITHDRAWN | NCT00937170 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Sliding Hip Screw | Other | Approved | Femoral Neck Fractures | COMPLETED | NCT00555945 |
| Gamma3 intramedullary nail (Stryker) | Other | Approved | Femoral Neck Fractures | COMPLETED | NCT00555945 |
| Interspinous Process Decompression | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| MILD | Other | Preclinical | Lumbar Spinal Stenosis | RECRUITING | NCT03072927 |
| Total knee | Other | Approved | Osteoarthritis | COMPLETED | NCT01135030 |
| Transgastric endoscopic peritoneoscopy. | Other | Phase EARLY_PHASE1 | Pancreatic Cancer | COMPLETED | NCT00427752 |
| Tritanium acetabular component | Other | Phase PHASE4 | Osteoarthritis | UNKNOWN | NCT01618084 |
| uncemented total hip arthroplasty | Other | Phase PHASE4 | Patients With Osteoarthritis of the Hip Joint Elligable for a Uncemented Hipprosthesis | COMPLETED | NCT01695213 |
| Iliac Crest Allograft with locked plate | Other | Phase PHASE4 | Adult Acquired Flatfoot | WITHDRAWN | NCT00949897 |
| Biofoam | Other | Phase PHASE4 | Adult Acquired Flatfoot | WITHDRAWN | NCT00949897 |
| Endovascular treatment of intracranial aneurysm. | Drug | Preclinical | Intracranial Aneurysm | COMPLETED | NCT00928265 |
| Triathlon Periapatite (PA)-coated Tibial Component | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT01180582 |
| Advance Biofoam porous metal backed tibial component with or without screw augmentation | Other | Approved | Osteoarthritis | COMPLETED | NCT00657956 |
| INBONE™ Total Ankle Prosthesis with Long Talar Stem | Other | Approved | Arthritis | TERMINATED | NCT01641848 |
| INBONE™ Total Ankle Prosthesis with Long Talar Stem | Other | Approved | Arthritis | TERMINATED | NCT01641848 |
| Wingspan Stent System with Gateway PTA Balloon Catheter | Other | Preclinical | Intracranial Atherosclerosis | COMPLETED | NCT00929383 |
| Wingspan Stent System with Gateway PTA Balloon Catheter | Other | Preclinical | Intracranial Atherosclerosis | COMPLETED | NCT00929383 |
| Rotator Cuff Repair without augmentation | Other | Approved | Rotator Cuff Tear | COMPLETED | NCT00456781 |
| Augmentation | Other | Approved | Rotator Cuff Tear | COMPLETED | NCT00456781 |
| Omnifit HA Hip Stem | Other | Approved | Arthroplasty, Replacement, Hip | TERMINATED | NCT00958347 |
| Near Infrared Fluorescence Cholangiography (NIRF-C) | Other | Phase PHASE1 | Acute Cholecystitis | COMPLETED | NCT02070627 |
| Indocyanine Green (ICG) | Other | Phase PHASE1 | Acute Cholecystitis | COMPLETED | NCT02070627 |
| Merci Retriever | Other | Approved | Ischemic Stroke | COMPLETED | NCT00318071 |
| Accolade® TMZF® Hip Stem | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT00957658 |
| Scorpio® CR Total Knee System | Other | Approved | Arthropathy of Knee | TERMINATED | NCT00965146 |
| Stroke team simulation training | Other | Preclinical | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | COMPLETED | NCT03228251 |
| Stroke team simulation training | Other | Preclinical | Stroke, Thrombolysis, Thrombectomy, Simulation Training, Patient Safety | COMPLETED | NCT03228251 |
| ADM/MDM hip | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT04019925 |
| TransForm™ Occlusion Balloon Catheter | Other | Preclinical | Intracranial Aneurysms | COMPLETED | NCT01949779 |
| TransForm™ Occlusion Balloon Catheter | Other | Preclinical | Intracranial Aneurysms | COMPLETED | NCT01949779 |
| Mechanical Thrombectomy | Other | Preclinical | Ischemic Stroke | COMPLETED | NCT00478478 |
| Conexa Reconstructive Tissue Matrix | Other | Approved | Rotator Cuff Tear | COMPLETED | NCT01025037 |
| Stryker Triathlon Tritanium primary knee | Other | Preclinical | Osteoarthritis of the Knee | UNKNOWN | NCT02373761 |
| Normal saline | Other | Phase PHASE2 | Cardiac Surgery | TERMINATED | NCT00586976 |
| Ropivacaine | Other | Phase PHASE2 | Cardiac Surgery | TERMINATED | NCT00586976 |
| Normal saline | Other | Phase PHASE2 | Cardiac Surgery | TERMINATED | NCT00586976 |
| Ropivacaine | Other | Phase PHASE2 | Cardiac Surgery | TERMINATED | NCT00586976 |
| Mechanical Thrombectomy | Other | Phase PHASE4 | Ischemic Stroke | COMPLETED | NCT01088672 |
| Mechanical Thrombectomy | Other | Approved | Ischemic Stroke | COMPLETED | NCT01270867 |
| Near Infrared Cholangiography Fluorescence (NIRF-C) | Other | Approved | Cholecystitis | COMPLETED | NCT02070640 |
| Injection of indocyanine green (ICG) | Other | Approved | Cholecystitis | COMPLETED | NCT02070640 |
| Motion analysis | Other | Approved | Arthropathy of Knee Joint | COMPLETED | NCT00967161 |
| Total Knee Arthroplasty | Other | Approved | Arthropathy of Knee Joint | COMPLETED | NCT00967161 |
| Motion analysis | Other | Approved | Arthropathy of Knee Joint | COMPLETED | NCT00967161 |
| Total Knee Arthroplasty | Other | Approved | Arthropathy of Knee Joint | COMPLETED | NCT00967161 |
| GDC® coils for endovascular aneurysm occlusion | Other | Phase PHASE4 | Intracranial Aneurysms | COMPLETED | NCT00396981 |
| Matrix 2® coils for endovascular aneurysm occlusion | Other | Phase PHASE4 | Intracranial Aneurysms | COMPLETED | NCT00396981 |
| any knee joint arthroplasty device | Device | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT01132365 |
| any knee joint arthroplasty device | Device | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT01132365 |
| Ambulatory continuous femoral nerve block for 100 hours | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00419276 |
| OmniFit® Series II Insert/OmniFit® PSL® Microstructured Acetabular Shell | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT00960206 |
| Alumina Insert/PSL® Microstructured Acetabular Shell or Secur-Fit® HA PSL® Acetabular Shell | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT00960206 |
| Trident® Ceramic Insert/Trident® AD HA Acetabular Shell | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT00960206 |
| Radiographic evaluation of previously implanted patients | Other | Preclinical | Arthrodesis | TERMINATED | NCT01366989 |
| Radiographic evaluation of previously implanted patients | Other | Preclinical | Arthrodesis | TERMINATED | NCT01366989 |
| Scandinavian Total Ankle Replacement System (STAR Ankle) | Other | Preclinical | Primary Arthrosis | COMPLETED | NCT01288586 |
| Restoration® Modular Revision Hip System | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT00962013 |
| Total Knee Arthroplasty using Robotic Arm | Other | Approved | Osteoarthritis, Knee | UNKNOWN | NCT03106558 |
| Total Knee Arthroplasty using Manual Instrumentation | Device | Approved | Osteoarthritis, Knee | UNKNOWN | NCT03106558 |
| Revision surgery with Dual Mobility Cup | Procedure | Preclinical | Primary Osteoarthritis | COMPLETED | NCT02062450 |
| Primary surgery with Dual Mobility Cup | Procedure | Preclinical | Primary Osteoarthritis | COMPLETED | NCT02062450 |
| Revision surgery with Dual Mobility Cup | Procedure | Preclinical | Primary Osteoarthritis | COMPLETED | NCT02062450 |
| Primary surgery with Dual Mobility Cup | Procedure | Preclinical | Primary Osteoarthritis | COMPLETED | NCT02062450 |
| Conventional technique | Other | Approved | Intertrochanteric Femur Fractures | COMPLETED | NCT02190435 |
| Stryker ADAPT computer-assisted navigation | Other | Approved | Intertrochanteric Femur Fractures | COMPLETED | NCT02190435 |
| Vitagel | Other | Approved | Failed Total Knee Arthroplasty | TERMINATED | NCT01923805 |
| BioFiber | Other | Preclinical | Full Thickness Rotator Cuff Tear | COMPLETED | NCT01849458 |
| Solution stem | Other | Approved | Hip Arthroplasty | COMPLETED | NCT00253838 |
| Restoration HA stem | Other | Approved | Hip Arthroplasty | COMPLETED | NCT00253838 |
| Trident® X3 Polyethylene Insert | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT00958191 |
| LFIT™ Femoral Heads With X3® Insert | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT00510458 |
| Symax uncemented hip stem | Other | Approved | Hip Osteoarthritis | COMPLETED | NCT03469687 |
| fixed bearing total knee prosthesis | Other | Phase PHASE4 | Arthritis of the Knee Joint | COMPLETED | NCT02892838 |
| mobile bearing knee system for total knee arthroplasty | Other | Phase PHASE4 | Arthritis of the Knee Joint | COMPLETED | NCT02892838 |
| Surgical Curettage for benign bone lesion | Other | Approved | Bone Lesion | COMPLETED | NCT03509480 |
| Medical Management | Other | Approved | Ischemic Stroke | COMPLETED | NCT02142283 |
| Trevo Thrombectomy Procedure | Procedure | Approved | Ischemic Stroke | COMPLETED | NCT02142283 |
| Medical Management | Other | Approved | Ischemic Stroke | COMPLETED | NCT02142283 |
| Trevo Thrombectomy Procedure | Procedure | Approved | Ischemic Stroke | COMPLETED | NCT02142283 |
| Volar Plate Fixation | Other | Approved | Distal Radius Fractures | COMPLETED | NCT00654615 |
| Intramedullary Radius Fixation (Micronail) | Other | Approved | Distal Radius Fractures | COMPLETED | NCT00654615 |
| Robotic-arm assisted partial knee arthroplasty | Other | Preclinical | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03668691 |
| Robotic-arm assisted partial knee arthroplasty | Other | Preclinical | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03668691 |
| Robotic-arm assisted medical MCK implant | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03668717 |
| Triathlon® CR Total Knee System | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT00957723 |
| Direct skeletal fixation of ITAP to lower limb amputees. | Other | Approved | Traumatic Amputation of Lower Extremity | COMPLETED | NCT02491424 |
| Cementless Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT01041937 |
| Cemented Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT01041937 |
| Sliding Hip Screws | Other | Approved | Femoral Neck Fractures | COMPLETED | NCT01380444 |
| Gamma3 Intramedullary Nails (Stryker) | Other | Approved | Femoral Neck Fractures | COMPLETED | NCT01380444 |
| Mechanical Thrombectomy | Other | Preclinical | Stroke | COMPLETED | NCT02446587 |
| Mechanical Thrombectomy | Other | Preclinical | Stroke | COMPLETED | NCT02446587 |
| Shoulder hemi-arthroplasty | Other | Preclinical | Localized, Primary Osteoarthritis | UNKNOWN | NCT02444299 |
| Shoulder hemi-arthroplasty | Other | Preclinical | Localized, Primary Osteoarthritis | UNKNOWN | NCT02424760 |
| Shoulder hemi-arthroplasty | Other | Preclinical | Localized, Primary Osteoarthritis | UNKNOWN | NCT02424760 |
| Zimmer PCR TKA | Other | Preclinical | Knee Prosthesis | COMPLETED | NCT01864434 |
| Stryker posterior cruciat retaining (PCR) total knee arthroplasty (TKA) | Other | Preclinical | Knee Prosthesis | COMPLETED | NCT01864434 |
| Zimmer PCR TKA | Other | Preclinical | Knee Prosthesis | COMPLETED | NCT01864434 |
| Stryker posterior cruciat retaining (PCR) total knee arthroplasty (TKA) | Other | Preclinical | Knee Prosthesis | COMPLETED | NCT01864434 |
| TRAP | Other | Preclinical | Stroke, Ischemic | TERMINATED | NCT03199404 |
| Wingspan Stent System | Other | Approved | Intracranial Atherosclerosis | COMPLETED | NCT02034058 |
| Wingspan Stent System | Other | Approved | Intracranial Atherosclerosis | COMPLETED | NCT02034058 |
| Unicompartmental knee arthroplasty with the Mako Robotic Arm-assisted system. | Other | Approved | Clinical Outcomes | COMPLETED | NCT03354195 |
| Endovascular Treatment (EVT) | Drug | Phase PHASE1 | Acute Stroke | COMPLETED | NCT02618031 |
| Blood ion levels | Other | Approved | Osteoarthritis | COMPLETED | NCT00380549 |
| Complication rate | Other | Approved | Osteoarthritis | COMPLETED | NCT00253877 |
| Complication rate | Other | Approved | Osteoarthritis | COMPLETED | NCT00253877 |
| Total knee arthroplasty with mechanical ancillary | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT03566875 |
| Total knee arthroplasty with the Stryker's MAKO™ system | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT03566875 |
| Total knee arthroplasty with mechanical ancillary | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT03566875 |
| Total knee arthroplasty with the Stryker's MAKO™ system | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT03566875 |
| Neuroform Atlas Stent System | Other | Preclinical | Intracranial Aneurysm | UNKNOWN | NCT04162483 |
| Reverse shoulder arthroplasty utilizing Blueprint Software | Other | Approved | Reverse Shoulder Replacement | UNKNOWN | NCT04474665 |
| Group TKA revision | Other | Preclinical | Knee Arthroplasty, Total | COMPLETED | NCT03898544 |
| Group primary TKA | Other | Preclinical | Knee Arthroplasty, Total | COMPLETED | NCT03898544 |
| Pinpoint Endoscopic Fluorescence Imaging System | Other | Approved | Laparoscopic Cholecystectomy | WITHDRAWN | NCT04561583 |
| LED light source system for endoscope | Other | Approved | Laparoscopic Cholecystectomy | WITHDRAWN | NCT04561583 |
| Ureteral stent (Cook Ireland Ltd.) | Other | Approved | Lower Abdominal Surgery | WITHDRAWN | NCT04561414 |
| LED light source system for endoscope | Other | Approved | Lower Abdominal Surgery | WITHDRAWN | NCT04561414 |
| JointCOACH | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT03499028 |
| JointCOACH | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT03499028 |
| Total Ankle Replacement Prosthesis | Other | Preclinical | Ankle Arthroplasty | TERMINATED | NCT03575975 |
| Wound Debridement | Other | Approved | Diabetic Foot Ulcers | COMPLETED | NCT01353495 |
| APM Graft (BIOTAPE XMTM) | Other | Approved | Diabetic Foot Ulcers | COMPLETED | NCT01353495 |
| Wound Debridement | Other | Approved | Diabetic Foot Ulcers | COMPLETED | NCT01353495 |
| APM Graft (BIOTAPE XMTM) | Other | Approved | Diabetic Foot Ulcers | COMPLETED | NCT01353495 |
| Surpass Flow Diverter(s) | Other | Preclinical | Cerebral Aneurysm | TERMINATED | NCT02281721 |
| MRI | Other | Approved | Chronic Hip Pain | COMPLETED | NCT03469817 |
| MRI | Other | Approved | Chronic Hip Pain | COMPLETED | NCT03469817 |
| Triathlon TS Knee System | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT00958789 |
| SNAP monitor; Bispectral Index Monitor (BIS Monitor) | Other | Approved | Anesthesia, General | COMPLETED | NCT00829803 |
| Computer assisted navigation | Other | Approved | Total Knee Arthroplasty | WITHDRAWN | NCT00409266 |
| Triathlon total knee implant | Other | Preclinical | Arthroplasties, Knee Replacement | COMPLETED | NCT03272178 |
| Depuy total knee implant | Other | Preclinical | Arthroplasties, Knee Replacement | COMPLETED | NCT03272178 |
| Rejuvenate Modular Hip | Other | Approved | Arthroplasty, Replacement, Hip | COMPLETED | NCT01257568 |
| CMC I prosthesis | Other | Approved | Arthropathy of Hand | UNKNOWN | NCT05267964 |
| Epping resection arthroplasty | Other | Approved | Arthropathy of Hand | UNKNOWN | NCT05267964 |
| Trevo® Retriever | Other | Preclinical | Real World Data in China | COMPLETED | NCT03554850 |
| Stereotactic guidance system | Other | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT02830997 |
| Total hip arthroplasty | Other | Approved | Prospective | RECRUITING | NCT04350255 |
| Surpass Flow Diverter | Other | Approved | Brain Aneurysm | COMPLETED | NCT01716117 |
| Aequalis Pyrocarbon Humeral Head | Other | Preclinical | Osteoarthritis | COMPLETED | NCT02525783 |
| Simpliciti™ Shoulder System | Other | Phase PHASE3 | Primary Generalized (Osteo)Arthritis | COMPLETED | NCT01390038 |
| Triathlon PKR | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT00966979 |
| Triathlon PKR | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT00966979 |
| Triathlon | Other | Approved | Knee Osteoarthritis | RECRUITING | NCT05842538 |
| Rhine Cervical Disc | Other | Preclinical | Radiculopathy | TERMINATED | NCT02403453 |
| Rhine Cervical Disc | Other | Preclinical | Radiculopathy | TERMINATED | NCT02403453 |
| Triathlon Knee | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02155712 |
| Triathlon Tritanium Knee | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02155712 |
| CO2 Laser Ablation | Other | Approved | Vulvar Intraepithelial Neoplasia (VIN) | COMPLETED | NCT02875561 |
| Sonopet Ultrasonic Aspirator | Other | Approved | Vulvar Intraepithelial Neoplasia (VIN) | COMPLETED | NCT02875561 |
| Trident II Tritanium Acetabular Shell for Revision | Other | Approved | Arthroplasty, Hip Revision | TERMINATED | NCT04317586 |
| Triathlon PSR Tibial Insert | Other | Approved | Arthroplasty | TERMINATED | NCT04618770 |
| Triathlon PSR Tibial Insert | Other | Approved | Arthroplasty | TERMINATED | NCT04618770 |
| ReUnion System with a Small-Diameter Glenosphere +6 mm offset | Other | Approved | Glenohumeral Joint Degeneration | COMPLETED | NCT02768597 |
| ReUnion System with a Large-Diameter Glenosphere +6 mm offset | Other | Approved | Glenohumeral Joint Degeneration | COMPLETED | NCT02768597 |
| ReUnion System with a Small-Diameter Glenosphere +2 mm offset | Other | Approved | Glenohumeral Joint Degeneration | COMPLETED | NCT02768597 |
| ReUnion System with a Large-Diameter Glenosphere +2 mm offset | Other | Approved | Glenohumeral Joint Degeneration | COMPLETED | NCT02768597 |
| Triathlon® CR/Conventional Limb Alignment | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02539992 |
| Triathlon® CR/Neutral Overall Limb Alignment | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02539992 |
| Triathlon® CR/Kinematic Alignment | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02539992 |
| Triathlon CR Total Knee System | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT02535741 |
| Triathlon CS fixed bearing total knee prosthesis | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT02525588 |
| Triathlon CS fixed bearing total knee prosthesis | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT02525588 |
| Partial Knee Resurfacing | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02525562 |
| Total Knee Replacement | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02525562 |
| Triathlon PKR System with X3 insert | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02525562 |
| Scorpio NRG Total Knee System with X3 insert | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02525562 |
| Triathlon Total Knee System with X3 insert | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT02525562 |
| Primary total knee replacement (Scorpio NRG CR Total Knee System) | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT02524730 |
| Triathlon PS | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT02522728 |
| Triathlon CR | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT02522728 |
| Duracon total knee system | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT00436982 |
| Cemented Triathlon total knee system | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT00436982 |
| Robotic-Arm Assisted THA | Other | Approved | Surgery | COMPLETED | NCT03891199 |
| DePuy Attune with VELYS Robotic-Assistance | Other | Approved | Knee Osteoarthritis | NOT_YET_RECRUITING | NCT06284824 |
| Stryker Triathlon with MAKO Robotic-Arm | Other | Approved | Knee Osteoarthritis | NOT_YET_RECRUITING | NCT06284824 |
| Conventional Fluoroscopy | Other | Approved | Femoroacetabular Impingement | ACTIVE_NOT_RECRUITING | NCT04265222 |
| Hipcheck Software | Other | Approved | Femoroacetabular Impingement | ACTIVE_NOT_RECRUITING | NCT04265222 |
| Observational Study Post MAKO Robotic Surgery | Procedure | Preclinical | Osteoarthritis, Hip | COMPLETED | NCT03846791 |
| Observational Study Post MAKO Robotic Surgery | Procedure | Preclinical | Osteoarthritis, Hip | COMPLETED | NCT03846791 |
| Minimally invasive lapidus procedure with arthroscopy | Procedure | Approved | Hallux Valgus and Bunion | NOT_YET_RECRUITING | NCT06570590 |
| Minimally invasive lapidus procedure with no arthroscopy | Procedure | Approved | Hallux Valgus and Bunion | NOT_YET_RECRUITING | NCT06570590 |
| Knee prosthesis implementation without additional cement | Other | Approved | Total Knee Arthroplasty | RECRUITING | NCT04692714 |
| Knee prosthesis implementation with additional cement | Other | Approved | Total Knee Arthroplasty | RECRUITING | NCT04692714 |
| Vertebroplasty | Other | Preclinical | Osteoporotic Vertebral Compression Fractures | COMPLETED | NCT04795765 |
| Balloon kyphoplasty | Other | Preclinical | Osteoporotic Vertebral Compression Fractures | COMPLETED | NCT04795765 |
| SpineJack system | Other | Preclinical | Osteoporotic Vertebral Compression Fractures | COMPLETED | NCT04795765 |
| Vertebroplasty | Other | Preclinical | Osteoporotic Vertebral Compression Fractures | COMPLETED | NCT04795765 |
| Balloon kyphoplasty | Other | Preclinical | Osteoporotic Vertebral Compression Fractures | COMPLETED | NCT04795765 |
| SpineJack system | Other | Preclinical | Osteoporotic Vertebral Compression Fractures | COMPLETED | NCT04795765 |
| T2 Alpha Tibia Nailing System | Other | Preclinical | Tibial Fractures | COMPLETED | NCT04015167 |
| T2 Alpha Tibia Nailing System | Other | Preclinical | Tibial Fractures | COMPLETED | NCT04015167 |
| ReUnion RSA System | Other | Preclinical | Shoulder Arthroplasty | TERMINATED | NCT03880955 |
| Foot and Ankle Devices | Device | Preclinical | Arthritis | TERMINATED | NCT04118894 |
| Foot and Ankle Devices | Device | Preclinical | Arthritis | TERMINATED | NCT04118894 |
| ReUnion Reverse Shoulder Arthroplasty (RSA) | Other | Preclinical | Arthroplasty | TERMINATED | NCT04089371 |
| ReUnion Total Shoulder Arthroplasty (TSA) | Other | Preclinical | Arthroplasty | TERMINATED | NCT04089371 |
| Restoration ADM X3 Device | Device | Approved | Arthroplasty, Replacement, Hip | TERMINATED | NCT01420237 |
| MAKO THA 4.0 System | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT04646096 |
| TKR with alternative alignment method | Other | Approved | Osteo Arthritis Knee | ACTIVE_NOT_RECRUITING | NCT03196011 |
| TKR with mechanical alignment method | Other | Approved | Osteo Arthritis Knee | ACTIVE_NOT_RECRUITING | NCT03196011 |
| ReUnion TSA System | Other | Preclinical | Shoulder Arthroplasty | TERMINATED | NCT03858517 |
| Surpass Streamline Flow Diverter System | Other | Preclinical | Aneurysm, Intracranial | TERMINATED | NCT05544045 |
| Surpass Streamline Flow Diverter System | Other | Preclinical | Aneurysm, Intracranial | TERMINATED | NCT05544045 |
| Adjustable versus fixed suspensory loop femoral side graft fixation | Other | Approved | Anterior Cruciate Ligament Reconstruction | ACTIVE_NOT_RECRUITING | NCT03184922 |
| Blood levels drawn | Other | Approved | Hip Pain | COMPLETED | NCT03433742 |
| Gamma4 Nailing System | Other | Preclinical | Femoral Fracture | ACTIVE_NOT_RECRUITING | NCT05523635 |
| Free-hand/perfect circles technique | Other | Approved | Femur Fracture | COMPLETED | NCT05613257 |
| Distal targeting jig | Other | Approved | Femur Fracture | COMPLETED | NCT05613257 |
| Free-hand/perfect circles technique | Other | Approved | Femur Fracture | COMPLETED | NCT05613257 |
| Distal targeting jig | Other | Approved | Femur Fracture | COMPLETED | NCT05613257 |
| Tritanium® Primary Acetabular Shell | Other | Approved | Arthroplasty, Replacement, Hip | TERMINATED | NCT01063751 |
| SPY Portable Handheld Imaging | Other | Phase PHASE4 | Parathyroid Dysfunction | RECRUITING | NCT06169735 |
| Indocyanine green | Other | Phase PHASE4 | Parathyroid Dysfunction | RECRUITING | NCT06169735 |
| Mechanical Thrombectomy | Other | Preclinical | Ischemic Stroke | COMPLETED | NCT03845491 |
| Shoulder Arthroplasty | Other | Preclinical | Shoulder Arthroplasty and Fracture Repair | TERMINATED | NCT02047955 |
| Insignia uncemented Hip Stem | Other | Approved | Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05144191 |
| Total knee arthroplasy | Other | Approved | Osteo Arthritis Knee | COMPLETED | NCT04092153 |
| Secur-Fit Advanced Hip Stem | Other | Approved | Arthroplasty, Replacement, Hip | TERMINATED | NCT01917929 |
| Patellofemoral arthroplasty | Other | Preclinical | Patellofemoral Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT04772625 |
| Patellofemoral arthroplasty | Other | Preclinical | Patellofemoral Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT04772625 |
| ECMO resuscitation | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT03700125 |
| ECMO resuscitation | Other | Approved | Death, Sudden, Cardiac | COMPLETED | NCT03700125 |
| Cemented Triathlon CR Total Knee System | Other | Approved | Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02578446 |
| Uncemented Triathlon Tritanium CR Total Knee System | Other | Approved | Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02578446 |
| Cemented Triathlon CR Total Knee System | Other | Approved | Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02578446 |
| Uncemented Triathlon Tritanium CR Total Knee System | Other | Approved | Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02578446 |
| Restoration Anatomic Acetabular Shell | Other | Approved | Arthropathy | RECRUITING | NCT05591859 |
| Intra-arterial Thrombectomy | Other | Phase PHASE4 | Stroke | COMPLETED | NCT03263117 |
| General Anesthesia (GA) | Other | Phase PHASE4 | Stroke | COMPLETED | NCT03263117 |
| Sedation | Other | Phase PHASE4 | Stroke | COMPLETED | NCT03263117 |
| Triathlon Tritanium Cone Augments | Other | Approved | Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02521103 |
| Apple Watch and App | Other | Approved | Spine Disease | COMPLETED | NCT04379921 |
| Shoulder iD™ Primary Reversed Glenoid | Other | Preclinical | Rotator Cuff Tears | ACTIVE_NOT_RECRUITING | NCT05868148 |
| Shoulder iD™ Primary Reversed Glenoid | Other | Preclinical | Rotator Cuff Tears | ACTIVE_NOT_RECRUITING | NCT05868148 |
| Knee arthroplasty | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT01326156 |
| Simplex HV/Gentamicin Simplex HV bone cement | Other | Preclinical | Arthritis Knee | COMPLETED | NCT05659329 |
| Wire Cerclage | Other | Approved | Heart Diseases | NOT_YET_RECRUITING | NCT06660186 |
| Rigid Sternal Fixation | Other | Approved | Heart Diseases | NOT_YET_RECRUITING | NCT06660186 |
| Basivertebral nerve ablation | Other | Preclinical | Verteborgenic Low Back Pain | NOT_YET_RECRUITING | NCT07392333 |
| Aequalis Pyrocarbon Humeral Head | Other | Preclinical | Osteoarthritis of the Shoulder | ACTIVE_NOT_RECRUITING | NCT05049993 |
| FocusMotion app | Other | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| Fitbit tracking device | Device | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| FocusMotion knee brace | Other | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| Device: Robotic MAKO total knee | Device | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| FocusMotion app | Other | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| Fitbit tracking device | Device | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| FocusMotion knee brace | Other | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| Device: Robotic MAKO total knee | Device | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT05744895 |
| Mako cemented TKA | Other | Approved | Total Knee Replacement | RECRUITING | NCT06929871 |
| Mako cementless TKA | Other | Approved | Total Knee Replacement | RECRUITING | NCT06929871 |
| Tornier Perform Humeral - Stem | Other | Preclinical | Osteoarthritis Shoulder | RECRUITING | NCT05067543 |
| Stryker SPY-PHI Imaging Device | Device | Phase PHASE2 | Sarcoma | RECRUITING | NCT04719156 |
| Indocyanine green solution administered at 2.0mg/kg. | Other | Phase PHASE2 | Sarcoma | RECRUITING | NCT04719156 |
| Standard medical management | Other | Approved | Ischemic Stroke | RECRUITING | NCT05983757 |
| Experimental: endovascular thrombectomy in patients who suffer a distal medium vessel occlusion | Other | Approved | Ischemic Stroke | RECRUITING | NCT05983757 |
| Triathlon Hinge Knee (THK) System | Other | Preclinical | Knee Arthropathy | RECRUITING | NCT06379321 |
| Triathlon Hinge Knee (THK) System | Other | Preclinical | Knee Arthropathy | RECRUITING | NCT06379321 |
| INFINITY™ with ADAPTIS™ Technology Total Ankle System | Other | Preclinical | Arthritis, Rheumatoid | ACTIVE_NOT_RECRUITING | NCT04594993 |
| Surpass Evolve Flow Diverter System | Other | Preclinical | Intracranial Aneurysm | ACTIVE_NOT_RECRUITING | NCT06368622 |
| Citadel Embolization Device | Device | Approved | Unruptured Wide-neck Aneurysms | ACTIVE_NOT_RECRUITING | NCT04057352 |
| Surpass Evolve Flow Diverter System | Other | Approved | Aneurysm, Intracranial | ACTIVE_NOT_RECRUITING | NCT04195568 |
| Tornier Perform® Humeral System - Fracture | Other | Preclinical | Traumatic Arthropathy of Shoulder | ACTIVE_NOT_RECRUITING | NCT05773352 |
| Tornier Perform® Humeral System - Fracture | Other | Preclinical | Traumatic Arthropathy of Shoulder | ACTIVE_NOT_RECRUITING | NCT05773352 |
| Femoral Nail PF of the T2 Alpha Femur Antegrade GT/PF Nailing System | Other | Preclinical | Femoral Fracture | COMPLETED | NCT04015154 |
| Femoral Nail PF of the T2 Alpha Femur Antegrade GT/PF Nailing System | Other | Preclinical | Femoral Fracture | COMPLETED | NCT04015154 |
| Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System | Other | Preclinical | Femoral Fracture | ACTIVE_NOT_RECRUITING | NCT04015128 |
| pHLIP® ICG NIRF imaging | Other | Phase PHASE1 | Breast Cancer | RECRUITING | NCT05130801 |
| Arthrex InternalBrace | Other | Preclinical | Lateral Ankle Instability | COMPLETED | NCT06829667 |
| Flexband | Other | Approved | Lateral Ankle Instability | COMPLETED | NCT06638138 |
| Gamma4 Nailing System | Other | Preclinical | Femoral Fracture | COMPLETED | NCT05523635 |
Total products: 344