| Symbol | ZBH |
|---|---|
| Name | ZIMMER BIOMET HOLDINGS, INC. |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Industrial Specialties |
| Address | 345 EAST MAIN STREET, WARSAW, Indiana, 46580, United States |
| Telephone | +1 574 - 373-3333 |
| Fax | — |
| — | |
| Website | https://www.zimmerbiomet.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001136869 |
| Description | Zimmer Biomet designs, manufactures, and markets orthopedic reconstructive implants, as well as supplies and surgical equipment for orthopedic surgery. With the acquisitions of Centerpulse in 2003 and Biomet in 2015, Zimmer holds the leading share of the reconstructive market in the United States, Europe, and Japan. Roughly 70% of total revenue is derived from sales of large joints, another quarter comes from extremities, trauma, and related surgical products. Additional info from NASDAQ: |
2026-08-13 17:53
New Form SCHEDULE 13G/A - ZIMMER BIOMET HOLDINGS, INC. <b>Filed:</b> 2026-08-13 <b>AccNo:</b> 0001193125-26-349494 <b>Size:</b> 7 KB
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2026-07-23 17:16
New Form 3 - ZIMMER BIOMET HOLDINGS, INC. <b>Filed:</b> 2026-07-23 <b>AccNo:</b> 0002136215-26-000004 <b>Size:</b> 9 KB
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2026-07-16 19:13
📋 Upadhyay Suketu (Ex-Officer) plans to sell 8K shares of ZIMMER BIOMET HOLDINGS, INC. (at $92.86 each, total $712K) Filed: Jul 16, 2026 | ID: 005253
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2026-07-02 21:44
Hilado Maria Teresa 🟢 acquired 389 shares (1 derivative) of ZIMMER BIOMET HOLDINGS, INC. (ZBH) at $86.65 Transaction Date: Jun 30, 2026 | Filing ID: 000012
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2026-07-02 21:43
Kurdikar Devdatt 🟢 acquired 180 shares (1 derivative) of ZIMMER BIOMET HOLDINGS, INC. (ZBH) at $86.65 Transaction Date: Jun 30, 2026 | Filing ID: 000008
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2026-07-02 20:23
HAGEMANN ROBERT 🟢 acquired 317 shares (1 derivative) of ZIMMER BIOMET HOLDINGS, INC. (ZBH) at $86.65 Transaction Date: Jun 30, 2026 | Filing ID: 000010
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT00175162 | A Comparison of Fixation Method in Total Knee Arthroplasty - Low Viscosity Vers… | Na | Osteoarthritis | Withdrawn | — | 2010-12-01 | ClinicalTrials.gov |
| NCT02474121 | Safety and Efficacy of Autologous Concentrated Bone Marrow Aspirate for Critica… | — | Peripheral Arterial Disease | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT06287853 | Tapestry Rotator Cuff Repair PMCF | — | Rotator Cuff Tears | Suspended | 2026-12-28 | 2030-12-30 | ClinicalTrials.gov |
| NCT07421245 | OsseoFit Stemless Shoulder System (Anatomic) | — | Shoulder Injuries | Not_Yet_Recruiting | 2026-07-01 | 2036-01-01 | ClinicalTrials.gov |
| NCT07485829 | Zimmer Biomet-RibFix Titan | — | Rib Fracture | Recruiting | 2026-03-31 | 2028-03-01 | ClinicalTrials.gov |
| NCT05199870 | MDR - PMCF Study for RingLoc Bipolar Acetabular Cup and Endo II Femoral Heads | — | Hip Arthritis | Enrolling_By_Invitation | 2026-03-10 | 2027-03-01 | ClinicalTrials.gov |
| NCT07286513 | Persona SoluTion PPS Femur PMCF | — | Rhematoid Arthritis | Enrolling_By_Invitation | 2026-02-26 | 2037-12-01 | ClinicalTrials.gov |
| NCT07150221 | MDR Vivacit-E Elevated Study | — | Osteoarthritis (OA) of the Hip | Enrolling_By_Invitation | 2026-01-07 | 2027-12-01 | ClinicalTrials.gov |
| NCT06863428 | Mymobility Knee ROM | — | Knee Range of Motion | Completed | 2025-11-21 | 2026-03-09 | ClinicalTrials.gov |
| NCT07434505 | Comparison of Iliac Crest Marrow vs. Proximal Tibia Avitus® Bone Graft | Na | Bone Graft | Recruiting | 2025-11-06 | 2026-12-01 | ClinicalTrials.gov |
| NCT07104279 | Z1 Hip System: Post-Market Clinical Follow Up Study | — | Hip Osteoarthritis | Recruiting | 2025-10-13 | 2031-08-01 | ClinicalTrials.gov |
| NCT06971497 | Zimmer ActivBraid Rotator Cuff Repair (RCR) Study | — | Rotator Cuff Repair of the Shoulder | Recruiting | 2025-08-11 | 2029-08-01 | ClinicalTrials.gov |
| NCT06699160 | Refobacin Revision-3 Bone Cement Post-Market Study | — | Revision Arthroplasty | Withdrawn | 2025-08-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07080450 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the Composi… | — | Rotator Cuff Repairs | Recruiting | 2025-07-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT06788717 | MDR - Comprehensive Primary Revision Stems PMCF | — | Shoulder Pain | Enrolling_By_Invitation | 2025-06-19 | 2040-12-01 | ClinicalTrials.gov |
| NCT06920459 | Zimmer Biomet Shoulder Arthroplasty PMCF Study | — | Shoulder Fractures | Recruiting | 2025-04-29 | 2037-06-01 | ClinicalTrials.gov |
| NCT06032416 | DenCT Shoulder Bone Quality Evaluation | Na | Osteoarthritis Shoulder | Not_Yet_Recruiting | 2025-04-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07009912 | ROSA® Knee System V1.5 Pilot Study | Na | Knee Arthroplasty, Total | Completed | 2025-02-25 | 2026-02-17 | ClinicalTrials.gov |
| NCT06699134 | Hi-Fatigue G Bone Cement Retrospective Study | — | Total Hip and Knee Arthroplasties | Recruiting | 2024-11-19 | 2026-10-01 | ClinicalTrials.gov |
| NCT06615739 | Comprehensive SRS Regenerex Tissue Attachment | — | Arthroplasty Complications | Active_Not_Recruiting | 2024-10-22 | 2026-12-31 | ClinicalTrials.gov |
| NCT05943574 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the XtraFix… | — | Wrist Fracture | Completed | 2024-06-10 | 2025-11-14 | ClinicalTrials.gov |
| NCT05497206 | ROSA® Hip System THA PMCF | Na | Osteoarthritis, Hip | Terminated | 2024-06-05 | 2024-12-20 | ClinicalTrials.gov |
| NCT06267482 | Using ROSA for Challenging The TKA Standard of Care | Phase4 | Knee Osteoarthritis | Recruiting | 2024-04-16 | 2025-12-01 | ClinicalTrials.gov |
| NCT05578651 | A Prospective, Single Center, Observational Study to Assess the Rapid Recovery … | — | Rigid Plate Fixation | Withdrawn | 2024-03-01 | 2025-10-01 | ClinicalTrials.gov |
| NCT06089291 | Persona IQ Cohort Study | — | Osteo Arthritis Knee | Active_Not_Recruiting | 2024-02-20 | 2026-12-01 | ClinicalTrials.gov |
| NCT05339360 | ZNN Bactiguard Antegrade Femoral Nails PMCF Study | — | Femur Fracture | Recruiting | 2024-01-16 | 2027-12-01 | ClinicalTrials.gov |
| NCT05966519 | ROSA Knee Intraoperative Planning Flexibility Study | — | Osteo Arthritis Knee | Recruiting | 2024-01-05 | 2029-01-01 | ClinicalTrials.gov |
| NCT06153446 | Infection Consortium Study#1 | — | PJI | Completed | 2023-12-10 | 2025-09-04 | ClinicalTrials.gov |
| NCT05276674 | ZNN Bactiguard Retrograde Femoral Nails PMCF Study | — | Femoral Fracture | Recruiting | 2023-10-23 | 2027-12-01 | ClinicalTrials.gov |
| NCT05980234 | MDR - Longevity IT Oblique and Offset Liners | — | Non-inflammatory Degenerative Joint Disease (NIDJD) | Terminated | 2023-08-30 | 2024-11-07 | ClinicalTrials.gov |
| NCT05630053 | Cemented vs Cementless Persona Keel RCT | Na | Knee Pain Chronic | Active_Not_Recruiting | 2023-07-25 | 2032-12-01 | ClinicalTrials.gov |
| NCT05787821 | Persona OsseoTi Keel Compatibility Study (Total Knee Arthroplasty) | — | Knee Pain Chronic | Active_Not_Recruiting | 2023-06-28 | 2035-06-01 | ClinicalTrials.gov |
| NCT05037734 | A Randomized Controlled Trial for Partial Knee Arthroplasty | Na | Degenerative Joint Disease of Knee | Withdrawn | 2023-06-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT05587244 | G7 Freedom Constrained Vivacit-E Liners | Na | Osteoarthritis, Hip | Enrolling_By_Invitation | 2023-05-08 | 2038-12-01 | ClinicalTrials.gov |
| NCT05179005 | RibFix Advantage™ Post-Market Follow-Up | — | Rib Fractures | Terminated | 2023-04-20 | 2023-12-31 | ClinicalTrials.gov |
| NCT05548972 | G7 Dual Mobility With Vivacit-E or Longevity PMCF | Na | Hip Osteoarthritis | Enrolling_By_Invitation | 2023-03-20 | 2037-08-01 | ClinicalTrials.gov |
| NCT05215613 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the Zimmer®… | — | Proximal Humeral Fracture | Completed | 2023-03-15 | 2024-03-27 | ClinicalTrials.gov |
| NCT05616715 | Evaluation of Different Periodontal Plastic Surgery Techniques for Gummy Smile … | Na | Gummy Smile | Unknown | 2023-02-15 | 2023-12-15 | ClinicalTrials.gov |
| NCT05778162 | RISC Panel Remnant Sample Collection | — | Arthritis, Inflammatory | Completed | 2023-02-01 | 2024-11-12 | ClinicalTrials.gov |
| NCT05362864 | ZNN Bactiguard Cephalomedullary Nails PMCF Study | — | Osteotomy | Completed | 2023-01-23 | 2025-12-17 | ClinicalTrials.gov |
| NCT05685693 | ROSA Knee System vs Conventional Total Knee Arthroplasty | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2022-12-16 | 2035-12-01 | ClinicalTrials.gov |
| NCT05584553 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the ToggleL… | — | Bankart Lesions | Completed | 2022-12-02 | 2024-06-30 | ClinicalTrials.gov |
| NCT05735119 | Embody Post-Market Clinical Follow-Up Study | — | Tendon Injuries- Subscapularis | Active_Not_Recruiting | 2022-11-09 | 2028-06-01 | ClinicalTrials.gov |
| NCT05519228 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the ToggleL… | — | Epicondylitis of the Elbow | Completed | 2022-09-12 | 2024-02-20 | ClinicalTrials.gov |
| NCT05253976 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the NexGen … | — | Rheumatoid Arthritis | Withdrawn | 2022-09-01 | 2034-12-31 | ClinicalTrials.gov |
| NCT05019664 | Affixus Natural Nail System Humeral Nail PMCF | — | Humeral Fractures, Proximal | Active_Not_Recruiting | 2022-08-29 | 2027-08-01 | ClinicalTrials.gov |
| NCT05583448 | MDR ExploR Radial Head System PMCF | — | Elbow Injury | Enrolling_By_Invitation | 2022-08-16 | 2035-07-19 | ClinicalTrials.gov |
| NCT05998785 | Embody Insertional Achilles Tendinopathy | — | Insertional Achilles Tendinopathy | Terminated | 2022-08-02 | 2024-08-01 | ClinicalTrials.gov |
| NCT05215626 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the Zimmer®… | — | Acetabulum Fracture | Completed | 2022-08-01 | 2024-12-12 | ClinicalTrials.gov |
| NCT05351112 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the Anatomi… | — | Proximal Humerus Fracture | Recruiting | 2022-07-07 | 2034-01-21 | ClinicalTrials.gov |
| NCT05690776 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the Quattro… | — | Rotator Cuff Tears | Completed | 2022-06-17 | 2024-11-15 | ClinicalTrials.gov |
| NCT05327959 | A.L.P.S. Clavicle Plating System PMCF | Na | Clavicle Fracture | Active_Not_Recruiting | 2022-05-13 | 2027-03-01 | ClinicalTrials.gov |
| NCT04677907 | TRabecular Metal Economic and Clinical Knee Trial | Na | Total Knee Replacement | Recruiting | 2022-05-10 | 2035-06-30 | ClinicalTrials.gov |
| NCT05215600 | Anaverse™ Glenoid System and Its Instrumentation | — | Rotator Cuff Injuries | Terminated | 2022-05-06 | 2024-04-23 | ClinicalTrials.gov |
| NCT05320354 | Diagnosis and Bacterial Identification of Periprosthetic Joint Infection With M… | — | Periprosthetic Joint Infection | Unknown | 2022-04-25 | 2025-12-01 | ClinicalTrials.gov |
| NCT05358574 | PMCF Study on the Safety, Performance and Clinical Benefits Data of the Anatomi… | — | Revision of a Shoulder Prosthesis | Recruiting | 2022-04-22 | 2033-07-16 | ClinicalTrials.gov |
| NCT05022485 | Zimmer® Natural Nail® (ZNN) Bactiguard Tibia Post-Market Clinical Follow-up Stu… | — | Tibial Fractures | Recruiting | 2022-04-11 | 2027-07-01 | ClinicalTrials.gov |
| NCT04093739 | MDR - G7 Neutral and G7 Freedom Constrained Neutral Acetabular Liners | — | Hip Osteoarthritis | Withdrawn | 2022-04-01 | 2029-12-31 | ClinicalTrials.gov |
| NCT05219305 | Implant Stability in Autogenous Mineralized and Demineralized Dentin Grafts | Na | Edentulous Alveolar Ridge | Active_Not_Recruiting | 2022-04-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT06899659 | Evaluation on Safety and Effectiveness of the An All-inside, All-suture Menisca… | Na | Meniscal Tears | Completed | 2022-02-14 | 2024-04-29 | ClinicalTrials.gov |
| NCT05002959 | TESS V3 Modular Total Shoulder System PMCF | — | Osteoarthritis Shoulder | Terminated | 2022-02-01 | 2026-03-05 | ClinicalTrials.gov |
| NCT05146986 | RibFix Blu Thoracic Fixation System Versus Non-surgical Treatment in Non-flail … | — | Rib; Fracture | Recruiting | 2022-01-02 | 2026-12-30 | ClinicalTrials.gov |
| NCT04033692 | MDR-JuggerKnot Mini Soft Anchor in Maxillofacial TMJ | — | TMJ Disc Disorder | Withdrawn | 2021-12-01 | 2022-11-01 | ClinicalTrials.gov |
| NCT04931056 | A Post Market Clinical Follow-up Study on Biomet Microfixation HTR PEKK (Midfac… | — | Tumor | Completed | 2021-10-01 | 2023-11-30 | ClinicalTrials.gov |
| NCT04731077 | Avenir Complete Post-Market Clinical Follow-Up Study | Na | Osteoarthritis, Hip | Active_Not_Recruiting | 2021-09-27 | 2036-06-01 | ClinicalTrials.gov |
| NCT05006274 | Intraoperative Soft Tissue Balance in TKA | — | Osteoarthritis, Knee | Unknown | 2021-08-13 | 2023-12-01 | ClinicalTrials.gov |
| NCT04984291 | Zimmer Biomet Shoulder Arthroplasty PMCF | Na | Shoulder Fractures | Recruiting | 2021-07-28 | 2033-08-15 | ClinicalTrials.gov |
| NCT04754087 | G7 Acetabular System With Vivacit-E or Longevity Liner PMCF Study | Na | Total Hip Arthroplasty | Active_Not_Recruiting | 2021-07-07 | 2033-12-31 | ClinicalTrials.gov |
| NCT04982198 | Robotic-assisted Versus Conventional Total Knee Arthroplasty | Na | Total Knee Arthoplasty | Completed | 2021-07-07 | 2023-05-31 | ClinicalTrials.gov |
| NCT03892005 | PMCF Study of MOTIVATION HIP System in THA | — | Total Hip Arthroplasty | Suspended | 2021-07-01 | 2024-12-31 | ClinicalTrials.gov |
| NCT04730739 | FastFrame Knee Spanning and Damage Control Kit PMCF | Na | Fracture | Terminated | 2021-06-18 | 2024-07-22 | ClinicalTrials.gov |
| NCT04821154 | Persona Revision Knee System Outcomes | — | Arthroplasty Complications | Recruiting | 2021-06-14 | 2033-12-31 | ClinicalTrials.gov |
| NCT04817969 | Persona Ti-Nidium Post-Market Clinical Follow-up | Na | Knee Pain Chronic | Active_Not_Recruiting | 2021-06-01 | 2034-05-01 | ClinicalTrials.gov |
| NCT04518111 | Oxford UKA and HTO Post-market Clinical Study | — | Knee Osteoarthritis | Enrolling_By_Invitation | 2021-04-24 | 2024-12-31 | ClinicalTrials.gov |
| NCT04653051 | PMCF Study on the Safety, Performance and Clinical Benefits of the DVR Plating … | — | Distal Radius Fracture | Completed | 2021-03-12 | 2022-11-15 | ClinicalTrials.gov |
| NCT04348968 | Maxera Large Cups - Canada | — | Degenerative Joint Disease of Hip | Terminated | 2021-03-01 | 2021-03-25 | ClinicalTrials.gov |
| NCT04427722 | PMCF Study of MPS-Flex® Knee System in TKA | — | Total Knee Arthroplasty | Suspended | 2021-02-25 | 2024-12-31 | ClinicalTrials.gov |
| NCT04349046 | Exception Cementless Hip Stem | — | Osteoarthritis, Hip | Active_Not_Recruiting | 2021-01-01 | 2025-12-01 | ClinicalTrials.gov |
| NCT04338893 | ROSA Total Knee Post Market Study EMEA | Na | Knee Pain | Completed | 2020-12-15 | 2025-08-22 | ClinicalTrials.gov |
| NCT03167788 | Red Cell Rejuvenation for the Attenuation of Transfusion Associated Organ Injur… | Phase2 | Organ Failure, Multiple | Withdrawn | 2020-12-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT04923724 | Tourniquet on Total Knee Arthroplasty | Na | Arthritis Knee | Completed | 2020-11-01 | 2024-11-27 | ClinicalTrials.gov |
| NCT03414307 | Stereotactic, Robot-assisted Intracerebral Hemorrhage Clot Evacuation | Na | Intracerebral Hematoma | Withdrawn | 2020-09-30 | 2020-09-30 | ClinicalTrials.gov |
| NCT04228367 | JuggerStitch Post Market Clinical Follow-up Study | Na | Meniscus Tear, Tibial | Recruiting | 2020-09-25 | 2026-04-30 | ClinicalTrials.gov |
| NCT03969654 | ROSA Robot Used in Total Knee Replacement Post Market Study | Na | Knee Pain | Completed | 2020-05-01 | 2023-09-22 | ClinicalTrials.gov |
| NCT04163224 | Minimal Invasive Approach for Surgical Repair of Rib Fractures With a Novel Int… | — | Rib Fracture Multiple | Withdrawn | 2020-04-01 | 2020-12-30 | ClinicalTrials.gov |
| NCT04028687 | MDR - PMCF Study for Taperloc Complete Stems | — | Hip Arthritis | Recruiting | 2020-02-13 | 2032-02-12 | ClinicalTrials.gov |
| NCT04027140 | MDR - M/L Taper With Kinectiv Technology Stems and Necks | — | Hip Disease | Terminated | 2020-01-22 | 2024-11-05 | ClinicalTrials.gov |
| NCT04031209 | G7 Dual Mobility System Used in Total Hip Arthroplasty for the Treatment of Fem… | — | Hip Fractures | Active_Not_Recruiting | 2020-01-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT04003311 | MDR - Comprehensive Primary/Micro Stem & Versa-Dial Ti Humeral Head | — | Shoulder Pain | Enrolling_By_Invitation | 2019-12-13 | 2028-07-29 | ClinicalTrials.gov |
| NCT04258605 | ASHCOM Shoulder System and Its Related Instruments | — | Rotator Cuff Injuries | Terminated | 2019-12-10 | 2024-08-13 | ClinicalTrials.gov |
| NCT04093700 | MDR SureLock All-Suture Anchor | — | Shoulder Pain | Terminated | 2019-11-05 | 2022-11-08 | ClinicalTrials.gov |
| NCT04003272 | MDR - Comprehensive Reverse/Versa Dial Ti Glenosphere | — | Shoulder Pain | Enrolling_By_Invitation | 2019-10-28 | 2035-09-01 | ClinicalTrials.gov |
| NCT03681977 | Clinical Outcomes of MP Persona vs. Persona Knee-PS | Na | Osteoarthritis, Knee | Enrolling_By_Invitation | 2019-09-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT03914703 | MDR EZ Pass and Precision Flexible Reamer | — | Anterior Cruciate Ligament Injury | Completed | 2019-08-08 | 2024-04-08 | ClinicalTrials.gov |
| NCT04002518 | MDR - Biomet Cannulated Screws | — | Fractures, Bone | Active_Not_Recruiting | 2019-08-07 | 2026-10-01 | ClinicalTrials.gov |
| NCT04063943 | Long Term Sidus PMCF | Na | Osteoarthritis | Withdrawn | 2019-07-12 | 2020-03-31 | ClinicalTrials.gov |
| NCT03970629 | ROSA Total Knee Investigational Testing Authorization Study | Na | Knee Pain | Terminated | 2019-06-20 | 2021-11-23 | ClinicalTrials.gov |
| NCT03666598 | The Effects of a Tourniquet in Total Knee Arthroplasty. | Na | Osteoarthritis, Knee | Unknown | 2019-05-28 | 2022-12-01 | ClinicalTrials.gov |
| NCT03709693 | Clinical Outcomes in Patients Treated With SternaLock Blu | — | Cardiac Surgical Procedures | Terminated | 2019-05-14 | 2020-05-13 | ClinicalTrials.gov |
| NCT03807349 | N-Force Screws Augmented With N-Force Blue in Hip Fractures | Na | Intracapsular Proximal Femur Fracture | Terminated | 2019-02-21 | 2021-03-11 | ClinicalTrials.gov |
| NCT03870477 | THP Hip Fracture Plating System Study | Na | Femur Fracture | Terminated | 2019-01-16 | 2021-03-10 | ClinicalTrials.gov |
| NCT04103515 | Knee Kinematics for Subjects With Zimmer-Biomet Posterior Cruciate Retaining or… | — | Arthroplasty, Replacement, Knee | Completed | 2019-01-03 | 2020-11-06 | ClinicalTrials.gov |
| NCT03580772 | Persona MC vs Attune Total Knee Replacement Study | — | Knee Osteoarthritis | Terminated | 2018-11-26 | 2022-05-04 | ClinicalTrials.gov |
| NCT03737149 | A Prospective Multicenter Longitudinal Cohort Study of the Mymobility Platform | Na | Osteoarthritis, Knee | Completed | 2018-10-22 | 2025-04-15 | ClinicalTrials.gov |
| NCT03726554 | Post-Market Study of Comprehensive Reverse Augmented Glenoid and Mini Humeral T… | Na | Arthropathy of Shoulder Region | Active_Not_Recruiting | 2018-08-28 | 2030-02-01 | ClinicalTrials.gov |
| NCT03626038 | Post Market Clinical Follow-up (PMCF) Study of the A.L.P.S. Proximal Humerus Pl… | Na | Osteoarthritis | Active_Not_Recruiting | 2018-06-19 | 2026-12-01 | ClinicalTrials.gov |
| NCT03589300 | Persona TM Tibia Clinical Outcomes Study | Na | Osteoarthritis | Completed | 2018-04-30 | 2022-11-30 | ClinicalTrials.gov |
| NCT03481595 | Improvement of Patient Satisfaction and Overall Outcomes Using HealthLoop | Na | Arthroplasty, Replacement, Knee | Completed | 2018-04-17 | 2020-06-17 | ClinicalTrials.gov |
| NCT03494660 | SCP Hip Outcomes Study | — | Subchondral Cysts | Completed | 2018-03-27 | 2025-01-13 | ClinicalTrials.gov |
| NCT03430219 | Subchondroplasty Procedure in Patients With Bone Marrow Lesions | — | Bone Marrow Lesions | Completed | 2018-03-01 | 2023-03-16 | ClinicalTrials.gov |
| NCT03371212 | A Prospective Randomized Controlled Trial of Dual-Mobility Components in Primar… | Phase4 | Serum Metal Levels, Specifically Cobalt, Chromium, and Titanium | Active_Not_Recruiting | 2017-12-15 | 2036-12-01 | ClinicalTrials.gov |
| NCT03266874 | G7 BiSpherical Acetabular Shell PMCF Study | — | Rheumatoid Arthritis | Active_Not_Recruiting | 2017-12-10 | 2031-12-01 | ClinicalTrials.gov |
| NCT03282578 | Sternalock Versus Wires for Sternal Closure Study | Na | Cardiac Surgery | Completed | 2017-10-05 | 2018-11-25 | ClinicalTrials.gov |
| NCT03272373 | NexGen TM Tibia Clinical Outcomes Study | Na | Osteoarthritis | Completed | 2017-10-03 | 2023-03-31 | ClinicalTrials.gov |
| NCT03494348 | RSA Study of Persona TKA With CR vs MC Polyethylene | Na | Osteoarthritis, Knee | Unknown | 2017-10-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT03089047 | Rejuvenated RBC and VO2 Max in Healthy Subjects | Phase4 | Erythrocyte Transfusion | Terminated | 2017-09-29 | 2018-04-18 | ClinicalTrials.gov |
| NCT03312465 | Anatomical Shoulder Domelock System Study | — | Avascular Necrosis | Active_Not_Recruiting | 2017-09-28 | 2032-12-09 | ClinicalTrials.gov |
| NCT03227692 | Persona TKA With iASSIST Knee System and iASSIST Knee System | Na | Osteoarthritis, Knee | Completed | 2017-08-18 | 2019-12-02 | ClinicalTrials.gov |
| NCT03058380 | Stated-Preferences in Knee Arthroplasty | — | Arthritis | Completed | 2017-08-17 | 2018-06-01 | ClinicalTrials.gov |
| NCT02185365 | Evaluation of T1rho Magnetic Resonance Imaging for Diagnosis of Cartilage Lesio… | — | Developmental Dysplasia of the Hip | Unknown | 2017-07-25 | 2021-12-01 | ClinicalTrials.gov |
| NCT03182374 | nSTRIDE APS Versus Hyaluronic Acid for Knee Osteoarthritis | Na | Osteoarthritis, Knee | Completed | 2017-07-14 | 2023-01-30 | ClinicalTrials.gov |
| NCT03568123 | A Comparison of the Persona Total Knee Arthroplasty System Using CR or MC Polye… | Na | Knee Osteoarthritis | Completed | 2017-07-05 | 2021-10-14 | ClinicalTrials.gov |
| NCT03192124 | Evaluating Bactisure Wound Lavage in Orthopedic Wounds | — | Infection of Total Knee Joint Prosthesis | Completed | 2017-07-01 | 2019-03-22 | ClinicalTrials.gov |
| NCT03075865 | A Cohort Study for Clinical Evaluation of OmniMax MMF System | — | Mandibular Fractures | Completed | 2017-06-28 | 2019-06-28 | ClinicalTrials.gov |
| NCT03409666 | Randomized Controlled RSA Study Comparing the Taperloc Complete Versus the Tape… | Na | Hip Osteoarthritis | Completed | 2017-05-12 | 2020-11-06 | ClinicalTrials.gov |
| NCT03199391 | BioWick SureLock Clinical Outcomes Study | Na | Rotator Cuff Tear | Completed | 2017-04-26 | 2021-05-05 | ClinicalTrials.gov |
| NCT03112200 | Subchondroplasty® Knee RCT | Na | Bone Marrow Edema | Completed | 2017-03-29 | 2023-08-23 | ClinicalTrials.gov |
| NCT03196193 | CM Asia Nail With AS2 Without AS2 （AS2 Study） | Na | Trochanteric Fracture of Femur | Completed | 2017-03-21 | 2020-04-09 | ClinicalTrials.gov |
| NCT03087396 | A Longitudinal Outcomes Study of the Subchondroplasty® Procedure in the Foot/An… | — | Insufficiency Fractures | Completed | 2017-03-10 | 2023-08-23 | ClinicalTrials.gov |
| NCT03308929 | Prospective G7 Dual Mobility Total Hip PMCF | — | Clinical Outcomes | Active_Not_Recruiting | 2017-02-28 | 2029-02-28 | ClinicalTrials.gov |
| NCT04326010 | Prospective Clinical Follow-up of the Echo Bi-Metric Microplasty Stem for Total… | — | Hip Osteoarthritis | Terminated | 2017-02-20 | 2024-12-04 | ClinicalTrials.gov |
| NCT03034811 | Persona Partial Knee Clinical Outcomes Study | Na | Osteoarthritis | Active_Not_Recruiting | 2017-02-08 | 2030-09-01 | ClinicalTrials.gov |
| NCT02863926 | Use of Autologous Concentrated Bone Marrow Aspirate in Preventing Wound Complic… | Phase1 | Peripheral Artery Disease | Completed | 2017-01-06 | 2018-07-27 | ClinicalTrials.gov |
| NCT02998333 | Chronic Ankle Instability, Surgical Repair: Open Versus Closed | Na | Chronic Ankle Instability | Completed | 2017-01-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT03073941 | A Multicenter Prospective Randomized Control Study on Persona Total Knee System… | Na | Osteoarthritis, Knee | Active_Not_Recruiting | 2016-12-01 | 2031-12-31 | ClinicalTrials.gov |
| NCT03495232 | Persona Cohort Nordic Multicenter Study | — | Knee Arthropathy | Active_Not_Recruiting | 2016-11-01 | 2032-12-31 | ClinicalTrials.gov |
| NCT02905240 | Saline-Controlled Study of nSTRIDE APS for Knee Osteoarthritis | Na | Osteoarthritis | Completed | 2016-11-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT03148184 | Reverse Shoulder Replacement: Age 60 or Younger Outcomes | — | Shoulder Arthritis | Completed | 2016-11-01 | 2019-02-01 | ClinicalTrials.gov |
| NCT03302013 | All Ligaments Left In Knee Arthroplasty Trial | Na | Primary Osteoarthritis of Knee Nos | Unknown | 2016-09-05 | 2022-01-01 | ClinicalTrials.gov |
| NCT03151109 | Glenoid Bone Grafting for RTSA: Clinical & Radiographic Outcomes | — | Osteo Arthritis Shoulders | Completed | 2016-09-01 | 2021-06-01 | ClinicalTrials.gov |
| NCT02447653 | Hydroxyapatite (HA) Coating Versus Plasma Porous Spray (PPS) in Press-fit Aceta… | Na | Osteoarthritis | Completed | 2016-07-15 | 2021-12-31 | ClinicalTrials.gov |
| NCT02897453 | Safety and Efficacy Study of Spinal Tethering | — | Adolescent Idiopathic Scoliosis | Unknown | 2016-07-06 | 2022-10-01 | ClinicalTrials.gov |
| NCT04011488 | Shared Decision Making and How It Impacts the Patient Understanding | Na | Knee Osteoarthritis | Terminated | 2016-06-01 | 2019-06-30 | ClinicalTrials.gov |
| NCT02695329 | Vanguard TKA With KneeAlign 2 and Without KneeAlign 2 | Na | Osteoarthritis, Knee | Completed | 2016-05-24 | 2018-10-26 | ClinicalTrials.gov |
| NCT02504112 | Zimmer CAS PSI X-Ray Knee in TKA (Total Knee Arthroplasty) | — | Total Knee Arthroplasty / Position of Customized X-Ray PSI Guides Using Optical Navigation | Completed | 2016-05-01 | 2018-05-01 | ClinicalTrials.gov |
| NCT02580643 | Prospective Post-Market Data Collection on Patients With Knee OA and Treated Wi… | — | Osteoarthritis, Knee | Completed | 2016-05-01 | 2019-06-30 | ClinicalTrials.gov |
| NCT02588040 | Recover L-PRP in Lateral Epicondylitis (REGP-11-00) | — | Lateral Epicondylitis | Terminated | 2016-05-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT03270982 | Comprehensive Segmental Revision System | — | Degenerative Disease | Active_Not_Recruiting | 2016-04-01 | 2035-12-01 | ClinicalTrials.gov |
| NCT02662881 | Biologically Assisted Core Decompression of the Femoral Head Using the PerFuse … | — | Avascular Necrosis of the Femoral Head | Unknown | 2016-03-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT02610192 | nSTRIDE APS in Females With Primary Patellofemoral Osteoarthritis | Na | Patellofemoral Osteoarthritis | Completed | 2016-03-01 | 2018-06-01 | ClinicalTrials.gov |
| NCT02717546 | Zimmer® MotionLoc® in Distal Tibia Fractures | — | Distal Tibia Fractures | Completed | 2016-02-01 | 2020-01-15 | ClinicalTrials.gov |
| NCT02601430 | BOLD MRI as a Surrogate of Improved Muscle Oxygenation Following Endovascular T… | Na | Peripheral Arterial Disease | Completed | 2016-02-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02656771 | Evaluation of Stability of Two Uncemented Hip Implants Used for Total Hip Arthr… | Na | Osteoarthritis, Hip | Unknown | 2016-01-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT03396224 | Avenir® Cemented Hip Stem - PMCF | — | Primary Osteoarthritis | Active_Not_Recruiting | 2015-11-18 | 2030-11-01 | ClinicalTrials.gov |
| NCT03456622 | BC Study of G7 Cup and Compatible Femoral Stems | — | Non-inflammatory Degenerative Joint Disease | Active_Not_Recruiting | 2015-11-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT02444052 | Evaluation of Zimmer Puros® Allograft vs. Creos™ Allograft for Alveolar Ridge P… | Na | Alveolar Bone Grafting | Completed | 2015-10-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT02686099 | Sternal Closure With SternaLock 360: First in Man Study | Na | Sternal Fracture | Completed | 2015-07-04 | 2018-01-15 | ClinicalTrials.gov |
| NCT02469662 | Clinical Outcomes Study of the Nexel Total Elbow | Na | Elbow Joint Destruction | Recruiting | 2015-06-01 | 2036-12-01 | ClinicalTrials.gov |
| NCT02518269 | A 3-Arm Study on G7 Acetabular Cup With Echo BiMetric Stem in Total Hip Arthrop… | Na | Osteoarthrosis | Active_Not_Recruiting | 2015-05-04 | 2030-11-30 | ClinicalTrials.gov |
| NCT02340390 | G7 Acetabular System vs. Exceed ABT Acetabular System in THA | Na | Osteoarthritis Arthritis | Completed | 2015-05-01 | 2018-11-01 | ClinicalTrials.gov |
| NCT03672370 | PMCF Study on the Safety and Performance of the Alloclassic Variall Cup Ceramic… | — | Avascular Necrosis | Terminated | 2015-03-24 | 2020-05-01 | ClinicalTrials.gov |
| NCT04461626 | Prospective Multi-centre Outcomes Study of Persona Knee System in Total Knee Ar… | — | Knee Osteoarthritis | Completed | 2014-11-19 | 2024-08-21 | ClinicalTrials.gov |
| NCT02220478 | Signature Acetabular Posterior/Lateral Data Collection | Na | Noninflammatory Degenerative Joint Disease | Terminated | 2014-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02350049 | Cementless Oxford Partial Knee Controlled Observational Study | — | Osteoarthritis | Completed | 2014-11-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT02262364 | Safety of NStride Autologous Protein Solution in the Treatment of Knee Osteoart… | Phase1 | Osteoarthritis, Knee | Completed | 2014-11-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02404727 | Evaluation of Cemented and Cementless Fixation of Dual-mobility Hip Prosthesis … | Na | Osteoarthritis, Hip | Completed | 2014-10-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02175576 | Randomized Controlled Clinical Outcomes of the Vanguard XP Bicruciate Knee Syst… | Na | Osteoarthritis | Terminated | 2014-10-01 | 2020-12-01 | ClinicalTrials.gov |
| NCT02269254 | Persona Versus NexGen | Na | Osteoarthritis Arthritis | Completed | 2014-09-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT02255383 | Persona Total Knee Arthroplasty Outcomes Study | Na | Knee Pain Chronic | Active_Not_Recruiting | 2014-07-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT02170558 | Enhanced Metal Reduction Techniques for Definitive CT Scanning to Assess Spinal… | — | Degenerative Disc Disease | Withdrawn | 2014-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02138890 | APSS-33-00: A Multicenter, Pilot Study of Autologous Protein Solution (APS) in … | Na | Osteoarthritis, Knee | Completed | 2014-05-01 | 2020-09-15 | ClinicalTrials.gov |
| NCT06720012 | Does the Use of Patient Specific Instrumentation Improve Outcomes in Knee Arthr… | Na | Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery | Active_Not_Recruiting | 2014-03-03 | 2024-12-01 | ClinicalTrials.gov |
| NCT02038140 | Zimmer Trabecular Metal Total Ankle PMCF | Na | Degenerative Arthritis | Active_Not_Recruiting | 2014-03-01 | 2027-12-01 | ClinicalTrials.gov |
| NCT02182843 | Cellentra Viable Cell Bone Matrix (VCBM) Anterior Cervical Discectomy and Fusio… | Na | Cervical Disc Degenerative Disorder | Completed | 2014-03-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT02307331 | RSA Study of Sirius Stem and Exceed Cup | Na | Osteoarthritis | Completed | 2014-03-01 | 2023-09-02 | ClinicalTrials.gov |
| NCT02429908 | Post-Market Surveillance Study of the TM Ardis Interbody Fusion System | Phase4 | Degenerative Disc Disease | Completed | 2014-03-01 | 2018-09-14 | ClinicalTrials.gov |
| NCT03409640 | Metal-on-metal Hip Replacement MRI Study | — | Hip Athroplasty Using M2a Magnum | Completed | 2014-01-17 | 2017-12-31 | ClinicalTrials.gov |
| NCT02084693 | COMPREHENSIVE® REVERSE SHOULDER Mini BasePlate | — | Rotator Cuff Tear Arthropathy | Completed | 2013-12-01 | 2019-06-01 | ClinicalTrials.gov |
| NCT01966848 | Comparison of Vanguard XP and Vanguard CR Total Knee Arthroplasties. A Trial Ev… | Na | Osteoarthritis | Unknown | 2013-11-01 | 2024-11-01 | ClinicalTrials.gov |
| NCT03423953 | Comprehensive Nano - Post Market Clinical Follow-Up Study | — | Osteoarthritis | Active_Not_Recruiting | 2013-10-30 | 2030-07-31 | ClinicalTrials.gov |
| NCT01859130 | Zimmer POLAR - Total Knee Arthroplasty (TKA) | Na | Osteoarthritis | Completed | 2013-10-21 | 2021-12-31 | ClinicalTrials.gov |
| NCT03226808 | Vivacit-E Post-market Follow-up Study | Na | Osteoarthritis | Active_Not_Recruiting | 2013-10-01 | 2028-06-30 | ClinicalTrials.gov |
| NCT02263209 | Investigation to Determine Safety of Taperloc Stems With BioGuard Coating When … | Na | Osteoarthritis of Hip | Active_Not_Recruiting | 2013-10-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT01934218 | Gel-One Treatment in Knee Osteoarthritis | Na | Osteoarthritis Knee | Completed | 2013-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01936259 | Comprehensive Shoulder System Nano IDE | Na | Joint Disease | Completed | 2013-08-01 | 2019-09-27 | ClinicalTrials.gov |
| NCT04076202 | Clinical Evaluation of Vanguard DD RP | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2013-07-11 | 2026-12-31 | ClinicalTrials.gov |
| NCT01878253 | Sidus Stem-Free Shoulder IDE Study | Na | Osteoarthritis | Completed | 2013-07-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT01410786 | Oxford Partial Knee Comparative Instrument Pilot Study | Na | Osteoarthritis, Knee | Completed | 2013-06-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01904019 | Comparison of ARPE Prosthesis With the Literature | — | Arthritis | Completed | 2013-04-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT01883492 | A Prospective Multi-center Study on Total Hip Arthroplasty With E1 | Na | Hip Osteoarthritis | Terminated | 2013-03-11 | 2019-03-15 | ClinicalTrials.gov |
| NCT01773226 | Evaluation of Intra-articular Injection of Autologous Protein Solution ("APS(TM… | Na | Gonarthrosis | Completed | 2013-03-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT02371382 | Multicentre Prospective Study to Evaluate Long-term Clinical Outcomes of the Si… | — | Arthroplasty, Replacement, Hip | Active_Not_Recruiting | 2013-03-01 | 2025-03-01 | ClinicalTrials.gov |
| NCT02087436 | Taperloc Complete Microplasty vs Taperloc Complete Standard: Randomized Control… | Na | Osteoarthritis | Completed | 2013-03-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02036931 | A Multicentre Observational Study to Evaluate Clinical Outcomes of the G7 Aceta… | — | Noninflammatory Degenerative Joint Disease | Completed | 2013-03-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT02087449 | Evaluate E1 Wear, Clinical Performance of E1 Liner in THA in Korean Patient Pop… | — | Osteoarthritis | Terminated | 2013-02-01 | 2024-12-12 | ClinicalTrials.gov |
| NCT01820611 | Arcos Revision Stem: Evaluation of Clinical Performance | — | Osteoarthritis | Completed | 2013-02-01 | 2021-06-14 | ClinicalTrials.gov |
| NCT02254980 | Migration and Head Penetration of Vitamin-E Diffused Cemented Polyethylene Cup … | Na | Total Hip Arthroplasty | Active_Not_Recruiting | 2013-02-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT01783483 | An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improvin… | Na | Coronary Artery Disease | Completed | 2013-01-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01754155 | A Prospective Radiostereometric Analysis and Clinical Evaluation of the Zimmer®… | Na | Radiostereometric Analysis | Unknown | 2013-01-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03372278 | PMCF Study on the Safety and Performance of the Zimmer® Maxera™ Acetabular Syst… | — | Rheumatoid Arthritis With Adequate Bone Quality | Active_Not_Recruiting | 2013-01-01 | 2028-12-01 | ClinicalTrials.gov |
| NCT02088372 | Prospective Multi-Center Study on Vanguard With E1 Bearing | — | Varus Deformity | Terminated | 2012-11-01 | 2021-02-01 | ClinicalTrials.gov |
| NCT01884077 | Total vs. Reverse Shoulder Replacement: Pain Relief Two Years After Surgery | Na | Arthritis | Terminated | 2012-11-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT01750606 | An MRI Investigation of Soft Tissues in Total Hip Arthroplasty | — | Tissue Reaction | Completed | 2012-10-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01700543 | Sidus(TM) Post Market Clinical Follow-up (PMCF) Study | — | Non-inflammatory Degenerative Joint Disease (NIDJD) | Completed | 2012-10-01 | 2026-03-04 | ClinicalTrials.gov |
| NCT01501955 | The Metaphyseal Hip Prosthesis - Total Hip | Na | Osteoarthritis of the Hip | Completed | 2012-10-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT01750840 | A Clinical Registry to Collect Patient Outcome Date for the BIOMET® Stimulator … | — | Fusion of Spine (Disease) | Terminated | 2012-10-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT03110224 | SCP® Observational Study of the Knee | — | Bone Marrow Edema | Terminated | 2012-09-18 | 2023-05-31 | ClinicalTrials.gov |
| NCT01763684 | Oxford Signature vs. Conventional Global Study | Na | Osteoarthritis | Terminated | 2012-09-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02851992 | A Prospective Study to Evaluate Long-term Clinical Outcomes of the GTS Cementle… | Na | Osteoarthritis, Hip | Terminated | 2012-09-01 | 2025-05-01 | ClinicalTrials.gov |
| NCT04114201 | Clinical Outcome and OR Resource Use of Total Knee Arthroplasty Using Patient-S… | Na | Gonarthrosis | Completed | 2012-08-02 | 2017-02-23 | ClinicalTrials.gov |
| NCT01906177 | A Prospective Munti-center Study on VANGUARD™ PS Total Knee Replacement System | — | Osteoarthritis | Completed | 2012-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01637051 | The Importance of Different Modularity of the Polyethylene Insert for Tibial Co… | Na | Arthrosis of the Knee | Active_Not_Recruiting | 2012-07-01 | 2026-08-01 | ClinicalTrials.gov |
| NCT00757354 | A Clinical Evaluation of Metal Ion Release From Metal-on-Metal Cementless Total… | Na | Osteoarthritis | Completed | 2012-06-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01461785 | The Use of Activated Platelet Rich Plasma (PRP) in Human Autologous Fat Transfer | Phase2 | Lipofilling | Completed | 2012-04-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01621893 | Evaluation of Subchondroplasty™ for Defects Associated With Bone Marrow Lesions | — | Bone Marrow Edema | Completed | 2012-03-26 | 2021-05-26 | ClinicalTrials.gov |
| NCT01528072 | Dynesys Spinal System Post Market 522 Study | Na | Degenerative Spondylolisthesis | Terminated | 2012-03-01 | 2017-04-01 | ClinicalTrials.gov |
| NCT01542580 | A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee | — | Osteoarthritis | Active_Not_Recruiting | 2012-03-01 | 2031-12-01 | ClinicalTrials.gov |
| NCT01549366 | Comparison of the Aspen Device Versus Pedicle Screws for Supplemental Posterior… | Na | Degeneration of Lumbar Intervertebral Disc | Completed | 2012-02-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01560273 | Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylol… | — | Spondylolisthesis | Terminated | 2012-02-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01463566 | Gender Solutions Natural Knee Post-Market Study | — | Osteoarthritis | Withdrawn | 2012-01-01 | 2025-01-01 | ClinicalTrials.gov |
| NCT01473134 | Safety and Efficacy of the Oxford Cementless Partial Knee System | Na | Osteoarthritis, Knee | Completed | 2011-12-01 | 2021-11-30 | ClinicalTrials.gov |
| NCT00760188 | Prospective Data Collection on Cementless Oxford Partial Knee | — | Arthroplasty, Replacement, Knee | Withdrawn | 2011-12-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01469806 | Patello-Femoral Joint Post Market Clinical Follow-up Within the Knee Registry | — | Arthritis | Withdrawn | 2011-11-01 | 2023-10-01 | ClinicalTrials.gov |
| NCT02169297 | Sub-Paraspinal Block in Nuss Patients. A Pilot Project | Phase4 | Pectus Excavatum | Completed | 2011-11-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT03357445 | AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study | Na | Primary Osteoarthritis | Active_Not_Recruiting | 2011-10-14 | 2027-04-27 | ClinicalTrials.gov |
| NCT01326832 | 10 Year Clinical Evaluation of Primoris Hip Component | — | Coxarthrosis | Active_Not_Recruiting | 2011-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT03970460 | Evaluation of Bone Mineral Density Changes Using Two Tibial Base Plate Designs … | Na | Knee Osteoarthritis | Unknown | 2011-08-05 | 2020-12-30 | ClinicalTrials.gov |
| NCT03672929 | Allofit® IT With HXPE in Total Hip Arthroplasty | — | Avascular Necrosis | Completed | 2011-06-05 | 2025-07-03 | ClinicalTrials.gov |
| NCT01343693 | MaxAn Post Market Surveillance Validation | — | DDD | Completed | 2011-06-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03672916 | Allofit® IT Ceramic Bearing System in Total Hip Arthroplasty | — | Avascular Necrosis of Hip | Completed | 2011-05-01 | 2023-04-01 | ClinicalTrials.gov |
| NCT04079114 | Post Market Clinical Follow-Up of the Zimmer Stafit Acetabular System | — | Osteoarthritis, Hip | Terminated | 2011-04-28 | 2019-07-15 | ClinicalTrials.gov |
| NCT01667887 | Plating of Distal Femur Fractures by Far Cortical Locking Using MotionLoc Screws | — | Fracture of Distal Femur | Completed | 2011-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01307384 | Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF… | — | Avascular Necrosis | Active_Not_Recruiting | 2011-03-29 | 2027-12-01 | ClinicalTrials.gov |
| NCT03112785 | Fitmore Versus CLS Stem in Total Hip Arthroplasty. Bilateral One-stage Operatio… | Na | Primary Hip Osteoarthritis | Active_Not_Recruiting | 2011-03-17 | 2026-06-01 | ClinicalTrials.gov |
| NCT01611493 | Osseotite Certain Prevail for the Preservation of Crestal Bone | Phase3 | Jaw, Edentulous, Partially | Unknown | 2011-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT03409718 | Database Retrieval for the Comprehensive Shoulder | — | Osteoarthritis of the Shoulder | Active_Not_Recruiting | 2011-02-24 | 2026-12-01 | ClinicalTrials.gov |
| NCT01064063 | Randomized Controlled Clinical Evaluation to Compare Vanguard Cruciate Retainin… | Na | Osteoarthritis | Completed | 2011-02-15 | 2022-05-10 | ClinicalTrials.gov |
| NCT03382652 | Continuum™ Metal Bearing System in Total Hip Arthroplasty | — | Avascular Necrosis | Completed | 2011-02-09 | 2022-10-22 | ClinicalTrials.gov |
| NCT01180595 | Roentgen Stereophotogrammetric Analysis (RSA) Trial Comparing Trabecular Metal … | Phase4 | Osteoarthritis | Completed | 2011-02-01 | 2019-09-01 | ClinicalTrials.gov |
| NCT03410940 | PMCF Study of the CLS Brevius Stem With Kinectiv Technology | — | Osteoarthritis | Terminated | 2011-01-07 | 2020-12-14 | ClinicalTrials.gov |
| NCT01480453 | Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder A… | — | Osteoarthritis | Terminated | 2011-01-02 | 2018-12-31 | ClinicalTrials.gov |
| NCT01247038 | A Multicentre Trial to Compare Two Articulating Bearing Surfaces as Used in Cem… | Na | Osteoarthritis | Terminated | 2011-01-01 | 2015-07-10 | ClinicalTrials.gov |
| NCT01480440 | Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder System | — | Osteoarthritis | Active_Not_Recruiting | 2011-01-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT01308463 | Discovery Elbow Long-Term Survivorship | — | Survivorship | Terminated | 2011-01-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT03431857 | Multi Centre Study on TESS V2 Shoulder System | — | Osteoarthritis Shoulder | Completed | 2010-10-20 | 2019-12-31 | ClinicalTrials.gov |
| NCT03343171 | Continuum Ceramic on Ceramic Bearing Post Market Clinical Follow-Up Study | — | Osteoarthritis | Active_Not_Recruiting | 2010-09-15 | 2025-09-01 | ClinicalTrials.gov |
| NCT01220505 | Post Market Surveillance to Evaluate the Effectiveness the Polaris Deformity Sp… | — | Spinal Deformity | Completed | 2010-09-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01308515 | Vanguard Knee Anterior Stabilized Versus Posterior Stabilized Bearing Study | Na | Osteoarthritis | Withdrawn | 2010-09-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01256216 | Signature Versus Computer Assisted Surgery Study | Na | Joint Disease | Completed | 2010-09-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01289834 | A Migration and Bone Density Study Comparing Hi-Fatigue Bone Cement and Palacos… | Na | Hip Arthritis | Completed | 2010-08-01 | 2024-01-01 | ClinicalTrials.gov |
| NCT01183260 | Evaluation of the Trabecular Metal™ Revision Hip Cup Using Bone Mineral Density… | Na | Revision, Joint | Completed | 2010-08-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01110070 | ChonDux for Filling Full Thickness Cartilage Defects in the Femoral Condyle of … | Na | Cartilage Defect | Terminated | 2010-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT04255394 | Exceed ABT Acetabular Cup Cementless System | — | Osteoarthritis | Completed | 2010-07-01 | 2022-03-31 | ClinicalTrials.gov |
| NCT01145157 | A Comparison Between Signature Total Knee Arthroplasty (TKA) to Conventional TK… | Na | Joint Disease | Completed | 2010-07-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01123850 | CopiOs Posterolateral Fusion Procedure | Phase2 | Spondylolisthesis | Terminated | 2010-06-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01049919 | Safety and Efficacy Study of Autologous Concentrated Bone Marrow Aspirate (cBMA… | Na | Critical Limb Ischemia | Terminated | 2010-06-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT01936415 | The Importance of Different Implant Surfaces of the Tibial Component for Migrat… | Phase4 | Artrosis of the Knee | Completed | 2010-05-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01103882 | Short-Term Clinical Outcome of Total Hip Arthroplasty Using Larger Diameter of … | — | Arthropathy of Hip | Completed | 2010-05-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT01050894 | Feasibility Study of Anti-inflammatory Cytokines in Whole Blood in Osteoarthrit… | — | Osteoarthritis | Completed | 2010-05-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01194817 | A Prospective, Randomized Study Comparing Cemented and Cementless Total Knee Re… | Na | Knee Osteoarthritis | Active_Not_Recruiting | 2010-04-01 | 2026-12-01 | ClinicalTrials.gov |
| NCT03404778 | Comprehensive Reverse Shoulder Data Collection | — | Arthropathy of Shoulder Region | Enrolling_By_Invitation | 2010-03-07 | 2036-12-01 | ClinicalTrials.gov |
| NCT01072019 | A Randomized Prospective Trial of Total Knee Arthroplasty Options Comparing Sta… | Na | Osteoarthritis of the Knee | Completed | 2010-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01092312 | Signature Personalised Patient Care System With the Vanguard Knee System Study | Na | Arthroplasty, Replacement, Knee | Terminated | 2010-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT04079127 | Avenir Müller Hip Stem Post Market Surveillance Study | — | Osteoarthritis, Hip | Completed | 2010-01-09 | 2019-08-31 | ClinicalTrials.gov |
| NCT03382665 | Post-market Surveillance Study With the HYPERION Hip Endoprosthesis System in D… | — | Osteoarthritis | Terminated | 2010-01-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT00858598 | Pro Osteon Bone Void Filler Study | — | Osteoarthritis | Withdrawn | 2009-12-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00754637 | Microplasty Tibial Tray Data Collection | — | Joint Disease | Withdrawn | 2009-12-01 | 2023-06-01 | ClinicalTrials.gov |
| NCT01016314 | Efficacy of the Aspen Spinous Process System in Anterior Lumbar Interbody Fusio… | Na | Degenerative Disc Disease | Withdrawn | 2009-11-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01010763 | A Study on M2a Magnum Total Hip Arthroplasty | Na | Degenerative Joint Disease | Completed | 2009-11-01 | 2017-04-28 | ClinicalTrials.gov |
| NCT01031732 | Evaluation of Four Surgical Techniques in Primary Total Hip Arthroplasty | Na | Arthroplasty, Replacement, Hip | Unknown | 2009-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT03664791 | Vanguard Rocc Post Market Surveillance | — | Osteoarthritis, Knee | Unknown | 2009-10-23 | 2025-12-31 | ClinicalTrials.gov |
| NCT01006148 | Comparison of a Bone Product to Bone Dust in Ossification of Small Calvarial De… | Phase4 | Metopic Craniosynostosis | Withdrawn | 2009-10-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01010269 | Vanguard Complete Knee Versus Vanguard High Flex Rotating Platform (RP) Knee St… | Na | Osteoarthritis | Completed | 2009-10-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01010828 | Review on Minimally Invasive Skin Incision in Vanguard PS Artificial Knee Joint… | Na | Gonarthrosis Patients Who Need Artificial Knee Joint Total Replacement | Completed | 2009-10-01 | 2012-03-31 | ClinicalTrials.gov |
| NCT00758641 | Platelet Rich Plasma to Treat Plantar Fasciitis | Phase4 | Plantar Fasciitis | Completed | 2009-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02247791 | Uncemented Compared to Cemented Femoral Stems in Total Hip Arthroplasty | Na | Hip Fractures | Unknown | 2009-09-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT03681639 | Metasul Monoblock Component™ Cup in a Hip Resurfacing Application With the Duro… | Na | Avascular Necrosis of Hip | Completed | 2009-08-01 | 2023-05-22 | ClinicalTrials.gov |
| NCT00881959 | Study of Root Coverage With Acellular Dermal Matrix: Puros® Dermis Versus Allod… | Na | Gingival Recession | Completed | 2009-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT02178020 | Outcome Study of Highly-cross Linked Polyethylene vs. Standard Polyethylene for… | — | Arthroplasty, Replacement, Knee | Unknown | 2009-07-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT00889265 | CopiOs® Pericardium Membrane for Localized Alveolar Ridge Augmentation | Na | Alveolar Ridge Defect | Completed | 2009-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00753090 | Vanguard™ Deep Dish Rotating Platform Knee Clinical Evaluation | Na | Osteoarthritis | Completed | 2009-06-01 | 2022-07-15 | ClinicalTrials.gov |
| NCT00983762 | Comparison of Functional Outcomes of Three Surgical Approaches in Knee Arthropl… | — | Knee Osteoarthritis | Terminated | 2009-06-01 | 2020-01-01 | ClinicalTrials.gov |
| NCT00679120 | Oxford Partial Knee Replacement. A Randomized Clinical Trial of Three Implant T… | Na | Osteoarthritis, Knee | Unknown | 2009-05-01 | 2024-08-01 | ClinicalTrials.gov |
| NCT00754520 | A Study Comparing Ceramic-on-metal Articulation to Metal-on-metal Articulation … | Na | Osteoarthritis | Completed | 2009-05-01 | 2021-12-01 | ClinicalTrials.gov |
| NCT00862316 | Oxford Unicompartmental Knee Arthroplasty With and Without Navigational Unit | Na | Knee Arthritis | Completed | 2009-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00715026 | Trilogy AB Acetabular Hip System Post Approval Study | Phase4 | Osteoarthritis | Terminated | 2009-04-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00854295 | Prospective Multicenter Post Approval Study of the LPS-Flex Mobile Bearing Knee | Na | Osteoarthritis | Completed | 2009-04-01 | 2021-06-01 | ClinicalTrials.gov |
| NCT00859976 | Study Comparing BoneMaster Hydroxyapatite Coating With Plasma-sprayed Hydroxyap… | Na | Arthropathy of Hip | Completed | 2009-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00859963 | Regenerex Tibial Tray Multi-Center Data Collection | — | Pain | Completed | 2009-03-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT00858442 | Platelet-Rich Plasma (PRP) in Reconstructive Surgery on Children With Retractab… | Na | Burns | Completed | 2009-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00804388 | Wear Measurements of E-Poly in an Uncemented THA With Either 32 or 36 mm Caput … | Na | Primary Arthrosis | Unknown | 2008-12-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00802477 | Application Of Autologous Blood Products During Modified Radical Mastectomy | Phase3 | Mastectomy | Unknown | 2008-12-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00819286 | Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain | Na | Sternal Wound Infection | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00913679 | A Comparison of Two Different Surgical Techniques in Hip Resurfacing Arthroplas… | Na | Osteonecrosis | Completed | 2008-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT00761046 | Retrospective Study on Cenos Stem With BoneMaster HA | — | Osteoarthritis | Withdrawn | 2008-10-01 | — | ClinicalTrials.gov |
| NCT00758719 | Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion System | — | Degenerative Disc Disease | Completed | 2008-09-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00750984 | A Comparison of Two Different Surgical Techniques for Total Hip Resurfacing | Na | Arthritis | Completed | 2008-09-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT00761423 | The Value of Platelet-Rich Plasma in Chronic Midportion Achilles Tendinopathy: … | Phase4 | Achilles Tendinopathy | Completed | 2008-08-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00708474 | OsseoFit™ Prospective Data Collection | Na | Bone Graft | Withdrawn | 2008-06-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00678236 | A Migration and Bone Density Study Comparing 2 Types of Bone Cement in the Opti… | Na | Osteoarthritis | Completed | 2008-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01462240 | LPS Flex Porous Femoral Components | — | Osteoarthritis | Withdrawn | 2008-05-20 | 2012-03-01 | ClinicalTrials.gov |
| NCT00758355 | Data Collection on ReCap/Magnum in Total Hip Replacement and Resurfacing | — | Total Hip Resurfacing | Completed | 2008-03-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT03411044 | Fitmore Hip Stem PMCF Study: A Multi-centre, Non-comparative, Prospective Post-… | — | Osteoarthritis | Completed | 2008-02-08 | 2023-06-10 | ClinicalTrials.gov |
| NCT00762723 | Clinical Outcomes of the Trinica(R) Anterior Lumbar Plate: Fixed Screws vs. Var… | Na | Degenerative Disc Disease | Terminated | 2008-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00665912 | Platelet-Rich and Concentrated Platelet-Poor Plasma to Reduce Air Leak Post-Lob… | Na | Lung Cancer | Completed | 2008-01-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT00633113 | Minimally Invasive Knee Replacement Outcomes (MIKRO) Study | Na | Knee Osteoarthritis | Completed | 2007-11-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00586170 | A Double-Blind Study on Adjunctive Use of PEMF in the Treatment of 5th Metatars… | Na | Nonunion of Fracture of Fifth Metatarsal | Terminated | 2007-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00545285 | Long-Term Multi-center Evaluation of E-Poly and Regenerex | Na | Osteoarthritis of Hip | Unknown | 2007-11-01 | 2023-05-01 | ClinicalTrials.gov |
| NCT00725894 | Pediatric Locking Nail for the Treatment of Femoral Fractures in Children | — | Femur Fracture | Completed | 2007-11-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT00551967 | Evaluation of the Wear of Vitamin E Treated Polyethylene Components in Primary … | Na | Osteoarthritis of Hip | Unknown | 2007-10-01 | 2022-12-01 | ClinicalTrials.gov |
| NCT00757289 | Platelet-rich-plasma Treating Tennis Elbow | Na | Pain | Completed | 2007-08-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT02465398 | Anatomical Shoulder™ Fracture PMCF Study | Na | Fracture | Completed | 2007-07-05 | 2024-03-11 | ClinicalTrials.gov |
| NCT00493558 | Spine Research With Roentgen Stereophotogrammetric Analysis | Phase4 | Spondylolisthesis | Completed | 2007-07-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00763113 | A Prospective Randomized Study on Vanguard Cruciate Retaining Versus Vanguard H… | Na | Total Knee Arthroplasty | Completed | 2007-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00746616 | Durom(R) Hip Resurfacing System Multicenter Trial | Phase3 | Advanced Hip Disease | Completed | 2007-06-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00474773 | Evaluation of Post Hospital Administration of Celecoxib Following Minimally Inv… | — | Pain Management | Completed | 2007-06-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00517452 | Platelet Rich Plasma Study in Lower Extremity Bypass Surgery | — | Atherosclerosis | Completed | 2007-05-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00755001 | Clinical Study on BiHapro Total Hip System With Different Surface Coatings | — | Osteoarthritis | Terminated | 2007-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00901329 | NexGen Gender Fixed Bearing Knee Versus NexGen Legacy Knee Posterior Stabilized… | Na | Total Knee Arthroplasty | Unknown | 2007-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00755144 | A Randomized Control Trial to Assess Early Clinical and Functional Outcome of t… | Na | Osteoarthritis | Completed | 2007-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00768924 | CopiOs(TM) Bone Void Filler in the Post-Harvest Iliac Crest | — | Spinal Fusions | Completed | 2007-03-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01113762 | Metal-metal Articulations Versus Standard 28 mm Cementless Total Hip Arthroplas… | Phase2 | Osteoarthritis, Hip | Unknown | 2007-02-01 | 2019-11-01 | ClinicalTrials.gov |
| NCT00484458 | Wallis Stabilization System for Low Back Pain | Phase3 | Low Back Pain | Unknown | 2007-01-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT00589485 | Total Knee Replacement Using Simplex® or Cobalt™ Bone Cement | — | Osteoarthritis | Withdrawn | 2006-11-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00492219 | Postoperative Function Following Partial and Total Knee Replacement | Na | Osteoarthritis | Terminated | 2006-10-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00833430 | Avascular Necrosis (AVN) Long-Term Follow-up | — | Avascular Necrosis | Terminated | 2006-06-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00726193 | Study to Analyze the Effects of EBI OsteoGen™ on the Surgical Reconstruction of… | — | Tibia Fracture Non Union Bone | Terminated | 2006-06-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00594893 | Study Comparing Mini-Incision Versus 2-Incision Approach for Total Hip Replacem… | Na | Osteoarthritis | Completed | 2006-06-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00791180 | Posterior Lateral Fusion (PLF) With Dynesys | — | Spondylolisthesis | Completed | 2006-03-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT00698152 | A Clinical Investigation of ArComXL® Polyethylene in Total Hip Replacement | — | Osteoarthritis | Completed | 2006-01-23 | 2016-01-15 | ClinicalTrials.gov |
| NCT00300326 | Computer-assisted Total Knee Arthroplasty (TKA) With Zimmer LPS Flex Knee System | Phase4 | Knee Arthroplasty | Terminated | 2006-01-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00751673 | TESS Shoulder Arthroplasty Data Collection | — | Arthritis | Terminated | 2006-01-01 | 2019-10-01 | ClinicalTrials.gov |
| NCT00514241 | Evaluate Use of Gravitational Platelet Separation System on Leg Wound Healing i… | Phase1 | Coronary Heart Failure | Completed | 2006-01-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01764984 | Bone Mineral Density Changes Under Two Tibial Components in Total Knee Arthropl… | Phase4 | Unilateral Primary Osteoarthritis of Knee | Completed | 2005-11-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT00762944 | Total Temporomandibular Joint Replacement System Post Approval Study | — | Arthroplasty | Completed | 2005-09-21 | 2008-09-21 | ClinicalTrials.gov |
| NCT00160797 | Total Knee Arthroplasty Outcome Study | Phase4 | Total Knee Replacement | Withdrawn | 2005-08-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00758472 | ReCap Total Hip Resurfacing Prospective Data Collection | — | Arthritis | Terminated | 2005-03-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01114646 | Functional Status, Morbidity and Mortality in Cemented Versus Press-Fit Hemiart… | Na | Femoral Neck Fracture | Completed | 2005-03-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00134537 | Wallis Mechanical Normalization System for Low Back Pain | Phase3 | Low Back Pain | Unknown | 2004-11-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00604734 | A Prospective Clinical Study On A Total Hip Resurfacing System | Na | Arthritis | Completed | 2004-10-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00116051 | A Comparison of Two Surface Materials (Tantalum Versus Titanium Fiber Mesh) of … | Na | Osteoarthritis | Completed | 2004-09-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00761956 | A Study to Compare the NexGen CR and CR-Flex Knee Implants | Na | Total Knee Arthroplasty | Completed | 2004-09-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00565786 | ArCom® and ArComXL® Polyethylene Data Collection | — | Osteoarthritis of Hip | Completed | 2004-07-01 | 2020-01-13 | ClinicalTrials.gov |
| NCT00175188 | An RSA and DEXA Study on Migration of Proximal Interphalangeal (PIP) Joint Pros… | Na | Osteoarthritis | Completed | 2004-06-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00726284 | Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc) | — | Degenerative Disc Disease | Completed | 2004-04-01 | 2007-12-06 | ClinicalTrials.gov |
| NCT00758329 | Retrospective Data Review of ReCap Total Hip Resurfacing | — | Osteoarthritis of the Hip | Withdrawn | 2004-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00792129 | MIS MiLIF Versus Open | — | Chronic Low Back Pain | Completed | 2004-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00698854 | A Clinical Investigation of the Vanguard™ Complete Knee System | — | Osteoarthritis | Completed | 2004-03-01 | 2024-03-01 | ClinicalTrials.gov |
| NCT00756431 | Clinical Evaluation on HA Coated Dynamic Hip Screws for Trochanteric Femoral Fr… | Na | Osteoarthritis | Withdrawn | 2004-01-01 | 2010-06-01 | ClinicalTrials.gov |
| NCT00116038 | A Comparison of Two Metal Surface Finishes on Femoral Components in Hip Arthrop… | Na | Osteoarthritis | Completed | 2004-01-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT02321683 | Evaluation of a New Coating in Cement Less Femoral Stems | Phase4 | Hip Osteoarthritis | Completed | 2003-12-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00758901 | ROCC Knee Data Collection | — | Arthritis of Knee | Terminated | 2003-11-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00138853 | A Roentgen Stereophotogrammetric Analysis on Migration of Knee Prostheses. | Na | Osteoarthritis | Completed | 2003-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00152165 | Use of Radiostereometric Analysis (RSA) Following Spinal Fusion Versus the DYNE… | — | Spinal Fusion | Completed | 2003-11-01 | — | ClinicalTrials.gov |
| NCT00757653 | Retrieval Study and Histological Examination Of A Hip Femoral Components With H… | Na | Femoral Neck Fractures | Terminated | 2003-10-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00589147 | A Prospective, Randomized, Controlled Study Comparing Three Tibial Component De… | Na | Total Knee Arthroplasty | Completed | 2003-08-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00261040 | Minimally Invasive Surgery of the Hip Versus Standard Approach | Na | Hip Arthroplasty | Completed | 2003-06-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00179088 | Safety of Non-delayed Weight Bearing After Total Hip Replacement With Non-Cemen… | Na | Osteoarthritis | Completed | 2003-05-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00759616 | Outcome Analysis of the Oxford Partial Knee Arthroplasty | Na | Knee Arthroplasty | Completed | 2003-04-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00754416 | S.E.S Shoulder Arthroplasty Data Collection | — | Arthritis | Terminated | 2003-03-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT00759057 | A Clinical Study of the Dynesys(R) Spinal System | Phase3 | Degenerative Spondylolisthesis or Retrolisthesis | Terminated | 2003-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00158418 | Cemented vs. Non-Cemented TSA for OA of the Shoulder | Phase3 | Osteoarthritis | Completed | 2002-08-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00585923 | Slotted Hole Versus Fixed Hole C-Tek | Na | Herniated Disc | Terminated | 2002-04-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00758758 | Performance of the Hedrocel(R) Cervical Fusion Device | Phase3 | Symptomatic Cervical Disc Disease | Completed | 2001-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00763386 | A Study to Compare the NexGen LPS and LPS-Flex Knee Implants | Na | Total Knee Arthroplasty | Completed | 2001-06-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT01488006 | Columbia Shoulder Study (CSS) | — | Osteoarthritis of Glenohumeral Joint | Completed | 2001-04-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT00726310 | Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolist… | — | Degenerative Disc Disease | Completed | 2000-05-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00591812 | Evaluation of the Compress Distal Femoral Replacement System | Phase1 | Lower Thighbone and Knee Joint Replacement | Completed | 2000-04-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00726128 | Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System | — | Trauma | Completed | 1998-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT03692351 | Osteolysis Development Around Uncemented Cups With or Without Screw Holes | Na | Arthroplasty Complications | Completed | 1994-06-15 | 2016-12-31 | ClinicalTrials.gov |
Total clinical trials: 370
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| Total knee arthroplasty | Other | Preclinical | Rhematoid Arthritis | ENROLLING_BY_INVITATION | NCT07286513 |
| Zimmer Biomet Persona Ti-Nidium Total Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT04817969 |
| GTS cementless stem | Other | Approved | Osteoarthritis, Hip | TERMINATED | NCT02851992 |
| Vivacit-E and Longevity (HXLPE) Liners | Other | Approved | Total Hip Arthroplasty | ACTIVE_NOT_RECRUITING | NCT04754087 |
| Biomet Comprehensive Shoulder System | Other | Preclinical | Osteoarthritis of the Shoulder | ACTIVE_NOT_RECRUITING | NCT03409718 |
| Total Knee Arthroplasty | Other | Preclinical | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT05787821 |
| Persona Revision Knee System | Other | Preclinical | Arthroplasty Complications | RECRUITING | NCT04821154 |
| Biomet Cannulated Screw: 3.0, 4.0, 5.0, 6.5, and 8.0mm screws. | Other | Preclinical | Fractures, Bone | ACTIVE_NOT_RECRUITING | NCT04002518 |
| Comprehensive Primary Revision Stems | Other | Preclinical | Shoulder Pain | ENROLLING_BY_INVITATION | NCT06788717 |
| Comprehensive Mini Humeral Tray | Other | Approved | Arthropathy of Shoulder Region | ACTIVE_NOT_RECRUITING | NCT03726554 |
| Comprehensive Reverse Porous Augmented Glenoid | Other | Approved | Arthropathy of Shoulder Region | ACTIVE_NOT_RECRUITING | NCT03726554 |
| Zimmer Trabecular Metal Total Ankle System | Other | Approved | Degenerative Arthritis | ACTIVE_NOT_RECRUITING | NCT02038140 |
| Nexel Total Elbow | Other | Approved | Elbow Joint Destruction | RECRUITING | NCT02469662 |
| OsseoFit Stemless Onlay | Other | Preclinical | Shoulder Injuries | NOT_YET_RECRUITING | NCT07421245 |
| OsseoFit Stemless Inlay | Other | Preclinical | Shoulder Injuries | NOT_YET_RECRUITING | NCT07421245 |
| Total knee arthroplasty | Other | Preclinical | Rhematoid Arthritis | ENROLLING_BY_INVITATION | NCT07286513 |
| Reverse TESS V3 | Other | Preclinical | Osteoarthritis Shoulder | TERMINATED | NCT05002959 |
| Anatomic TESS V3 | Other | Preclinical | Osteoarthritis Shoulder | TERMINATED | NCT05002959 |
| Comprehensive SRS Replacement | Other | Preclinical | Degenerative Disease | ACTIVE_NOT_RECRUITING | NCT03270982 |
| Shoulder Arthroplasty | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | COMPLETED | NCT01700543 |
| Alliance™ Glenoid | Other | Preclinical | Shoulder Fractures | RECRUITING | NCT06920459 |
| Persona IQ | Other | Preclinical | Osteo Arthritis Knee | ACTIVE_NOT_RECRUITING | NCT06089291 |
| Tapestry Biointegrative Implant | Other | Preclinical | Tendon Injuries- Subscapularis | ACTIVE_NOT_RECRUITING | NCT05735119 |
| Fracture fixation via Intramedullary Nailing | Other | Preclinical | Osteotomy | COMPLETED | NCT05362864 |
| Tapestry Biointegrative Implant | Other | Preclinical | Tendon Injuries- Subscapularis | ACTIVE_NOT_RECRUITING | NCT05735119 |
| Fracture fixation via Intramedullary Nailing | Other | Preclinical | Osteotomy | COMPLETED | NCT05362864 |
| Tapestry Biointegrative Implant | Other | Preclinical | Tendon Injuries- Subscapularis | ACTIVE_NOT_RECRUITING | NCT05735119 |
| Fracture fixation via Intramedullary Nailing | Other | Preclinical | Osteotomy | COMPLETED | NCT05362864 |
| Tapestry Biointegrative Implant | Other | Preclinical | Tendon Injuries- Subscapularis | ACTIVE_NOT_RECRUITING | NCT05735119 |
| Fracture fixation via Intramedullary Nailing | Other | Preclinical | Osteotomy | COMPLETED | NCT05362864 |
| Tapestry Biointegrative Implant | Other | Preclinical | Tendon Injuries- Subscapularis | ACTIVE_NOT_RECRUITING | NCT05735119 |
| Fracture fixation via Intramedullary Nailing | Other | Preclinical | Osteotomy | COMPLETED | NCT05362864 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | ACTIVE_NOT_RECRUITING | NCT05019664 |
| Acetabular implant, Monoblock cup | Other | Approved | Osteoarthritis | COMPLETED | NCT00116051 |
| Acetabular implant, Monoblock cup | Other | Approved | Osteoarthritis | COMPLETED | NCT00116051 |
| Femoral implant (Versys Fiber Metal Taper®) | Other | Approved | Osteoarthritis | COMPLETED | NCT00116038 |
| Femoral implant (Versys Fiber Metal Taper®) | Other | Approved | Osteoarthritis | COMPLETED | NCT00116038 |
| Avanta (PIP joint implant with a titanium porous coating) | Other | Approved | Osteoarthritis | COMPLETED | NCT00175188 |
| Avanta (PIP joint implant with a titanium porous coating) | Other | Approved | Osteoarthritis | COMPLETED | NCT00175188 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Radiostereometric Analysis beads inserted during surgery | Procedure | Preclinical | Spinal Fusion | COMPLETED | NCT00152165 |
| Radiostereometric Analysis beads inserted during surgery | Procedure | Preclinical | Spinal Fusion | COMPLETED | NCT00152165 |
| Uncemented Humeral Stem | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00158418 |
| Cemented Humeral Stem | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00158418 |
| Uncemented Humeral Stem | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00158418 |
| Cemented Humeral Stem | Other | Phase PHASE3 | Osteoarthritis | COMPLETED | NCT00158418 |
| NexGen LPS-Flex Fixed Bearing Knee prosthesis | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT00901329 |
| NexGen Gender Fixed Bearing Knee prosthesis | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT00901329 |
| NexGen LPS-Flex Fixed Bearing Knee prosthesis | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT00901329 |
| NexGen Gender Fixed Bearing Knee prosthesis | Other | Approved | Total Knee Arthroplasty | UNKNOWN | NCT00901329 |
| MIS-PL THA | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| MIS-AL THA | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| MIS-WJ | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| MIS-2 THA | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| MIS-PL THA | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| MIS-AL THA | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| MIS-WJ | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| MIS-2 THA | Other | Approved | Arthroplasty, Replacement, Hip | UNKNOWN | NCT01031732 |
| Total hip arthroplasty | Other | Approved | Primary Arthrosis | UNKNOWN | NCT00804388 |
| Total hip arthroplasty | Other | Approved | Primary Arthrosis | UNKNOWN | NCT00804388 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Standard Modified Radical Mastectomy | Other | Phase PHASE3 | Mastectomy | UNKNOWN | NCT00802477 |
| Application of autologous blood products. | Other | Phase PHASE3 | Mastectomy | UNKNOWN | NCT00802477 |
| Standard Modified Radical Mastectomy | Other | Phase PHASE3 | Mastectomy | UNKNOWN | NCT00802477 |
| Application of autologous blood products. | Other | Phase PHASE3 | Mastectomy | UNKNOWN | NCT00802477 |
| Total Disc Replacement | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00484458 |
| Interspinous process and dynamic stabilization (Wallis System) | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00484458 |
| Conservative Care | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00134537 |
| Interspinous process and dynamic stabilization | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00134537 |
| Conservative Care | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00134537 |
| Interspinous process and dynamic stabilization | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00134537 |
| Conservative Care | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00134537 |
| Interspinous process and dynamic stabilization | Other | Phase PHASE3 | Low Back Pain | UNKNOWN | NCT00134537 |
| Arthroscopy Alone | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| Subchondroplasty with Arthroscopy | Other | Approved | Bone Marrow Edema | COMPLETED | NCT03112200 |
| The Atavi System | Other | Preclinical | Chronic Low Back Pain | COMPLETED | NCT00792129 |
| The Atavi System | Other | Preclinical | Chronic Low Back Pain | COMPLETED | NCT00792129 |
| MIS™ Minimally Invasive Solutions™ TKA System | Other | Phase PHASE4 | Total Knee Replacement | WITHDRAWN | NCT00160797 |
| The Zimmer NexGen Legacy Knee System, non-modular uncemented tibia | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00589147 |
| The Zimmer NexGen Legacy Knee System, non-modular cemented tibia. | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00589147 |
| The Zimmer NexGen Legacy Knee System, modular cemented tibia | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00589147 |
| The Zimmer NexGen Legacy Knee System, non-modular uncemented tibia | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00589147 |
| The Zimmer NexGen Legacy Knee System, non-modular cemented tibia. | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00589147 |
| The Zimmer NexGen Legacy Knee System, modular cemented tibia | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00589147 |
| NexGen Legacy Posterior Stabilized Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763386 |
| NexGen LPS-Flex Fixed Bearing Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763386 |
| NexGen Legacy Posterior Stabilized Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763386 |
| NexGen LPS-Flex Fixed Bearing Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763386 |
| Osseotite Non Prevail Implant | Other | Phase PHASE3 | Jaw, Edentulous, Partially | UNKNOWN | NCT01611493 |
| Osseotite Prevail Implant | Other | Phase PHASE3 | Jaw, Edentulous, Partially | UNKNOWN | NCT01611493 |
| Osseotite Non Prevail Implant | Other | Phase PHASE3 | Jaw, Edentulous, Partially | UNKNOWN | NCT01611493 |
| Osseotite Prevail Implant | Other | Phase PHASE3 | Jaw, Edentulous, Partially | UNKNOWN | NCT01611493 |
| Posterior Pedicle Screw System | Other | Phase PHASE3 | Degenerative Spondylolisthesis or Retrolisthesis | TERMINATED | NCT00759057 |
| Posterior Pedicle Screw System | Other | Phase PHASE3 | Degenerative Spondylolisthesis or Retrolisthesis | TERMINATED | NCT00759057 |
| NexGen CR Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00761956 |
| NexGen CR-Flex Fixed Bearing Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00761956 |
| NexGen CR Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00761956 |
| NexGen CR-Flex Fixed Bearing Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00761956 |
| 2 Incision Approach | Other | Approved | Osteoarthritis | COMPLETED | NCT00594893 |
| Mini Incision Approach | Other | Approved | Osteoarthritis | COMPLETED | NCT00594893 |
| 2 Incision Approach | Other | Approved | Osteoarthritis | COMPLETED | NCT00594893 |
| Mini Incision Approach | Other | Approved | Osteoarthritis | COMPLETED | NCT00594893 |
| Total Knee Replacement | Other | Approved | Osteoarthritis | TERMINATED | NCT00492219 |
| Vanguard M fixed-bearing or Oxford mobile-bearing prostheses | Other | Approved | Osteoarthritis | TERMINATED | NCT00492219 |
| Total Knee Replacement | Other | Approved | Osteoarthritis | TERMINATED | NCT00492219 |
| Vanguard M fixed-bearing or Oxford mobile-bearing prostheses | Other | Approved | Osteoarthritis | TERMINATED | NCT00492219 |
| Trabecular Metal Intervertebral Cage with RSA beads | Other | Phase PHASE4 | Spondylolisthesis | COMPLETED | NCT00493558 |
| Trabecular Metal Intervertebral Cage with RSA beads | Other | Phase PHASE4 | Spondylolisthesis | COMPLETED | NCT00493558 |
| Trabecular Metal Intervertebral Cage with RSA beads | Other | Phase PHASE4 | Spondylolisthesis | COMPLETED | NCT00493558 |
| Durom Hip Resurfacing System | Other | Phase PHASE3 | Advanced Hip Disease | COMPLETED | NCT00746616 |
| Durom Hip Resurfacing System | Other | Phase PHASE3 | Advanced Hip Disease | COMPLETED | NCT00746616 |
| MPPA | Other | Approved | Knee Osteoarthritis | COMPLETED | NCT00633113 |
| MPPA | Other | Approved | Knee Osteoarthritis | COMPLETED | NCT00633113 |
| Refobacin Plus Bone Cement | Other | Approved | Osteoarthritis | COMPLETED | NCT00678236 |
| Refobacin Bone Cement R | Other | Approved | Osteoarthritis | COMPLETED | NCT00678236 |
| Refobacin Plus Bone Cement | Other | Approved | Osteoarthritis | COMPLETED | NCT00678236 |
| Refobacin Bone Cement R | Other | Approved | Osteoarthritis | COMPLETED | NCT00678236 |
| Refobacin Plus Bone Cement | Other | Approved | Osteoarthritis | COMPLETED | NCT00678236 |
| Refobacin Bone Cement R | Other | Approved | Osteoarthritis | COMPLETED | NCT00678236 |
| Anterior Cervical Discectomy and Fusion | Other | Phase PHASE3 | Symptomatic Cervical Disc Disease | COMPLETED | NCT00758758 |
| Anterior Cervical Discectomy and Fusion | Other | Phase PHASE3 | Symptomatic Cervical Disc Disease | COMPLETED | NCT00758758 |
| Regenerex | Other | Phase PHASE4 | Artrosis of the Knee | COMPLETED | NCT01936415 |
| Vanguard | Other | Phase PHASE4 | Artrosis of the Knee | COMPLETED | NCT01936415 |
| Regenerex | Other | Phase PHASE4 | Artrosis of the Knee | COMPLETED | NCT01936415 |
| Vanguard | Other | Phase PHASE4 | Artrosis of the Knee | COMPLETED | NCT01936415 |
| Trinica Anterior Lumbar Plate System | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT00762723 |
| Trinica Anterior Lumbar Plate System | Other | Approved | Degenerative Disc Disease | TERMINATED | NCT00762723 |
| PCA only | Other | Phase PHASE4 | Pectus Excavatum | COMPLETED | NCT02169297 |
| Ultrasound-guided Sub-Paraspinal Block | Other | Phase PHASE4 | Pectus Excavatum | COMPLETED | NCT02169297 |
| PCA only | Other | Phase PHASE4 | Pectus Excavatum | COMPLETED | NCT02169297 |
| Ultrasound-guided Sub-Paraspinal Block | Other | Phase PHASE4 | Pectus Excavatum | COMPLETED | NCT02169297 |
| CopiOs Pericardium Membrane | Other | Approved | Alveolar Ridge Defect | COMPLETED | NCT00889265 |
| Corticosteroid Injection | Other | Phase PHASE4 | Plantar Fasciitis | COMPLETED | NCT00758641 |
| L-PRP Injection | Other | Phase PHASE4 | Plantar Fasciitis | COMPLETED | NCT00758641 |
| Corticosteroid Injection | Other | Phase PHASE4 | Plantar Fasciitis | COMPLETED | NCT00758641 |
| L-PRP Injection | Other | Phase PHASE4 | Plantar Fasciitis | COMPLETED | NCT00758641 |
| The GPS™ II Platelet Concentrate Separation Kit | Other | Phase PHASE1 | Coronary Heart Failure | COMPLETED | NCT00514241 |
| The GPS™ II Platelet Concentrate Separation Kit | Other | Phase PHASE1 | Coronary Heart Failure | COMPLETED | NCT00514241 |
| Hip stem with Interloc Titanium surface + Bonemaster H.A | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with plasma spayed porous Titanium 6Al4V alloy + Bonemaster HA | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with plasma sprayed porous Ti 6Al4V alloy + plasma sprayed HA | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with Interloc Titanium surface + Bonemaster H.A | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with plasma spayed porous Titanium 6Al4V alloy + Bonemaster HA | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with plasma sprayed porous Ti 6Al4V alloy + plasma sprayed HA | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with Interloc Titanium surface + Bonemaster H.A | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with plasma spayed porous Titanium 6Al4V alloy + Bonemaster HA | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| Hip stem with plasma sprayed porous Ti 6Al4V alloy + plasma sprayed HA | Other | Approved | Femoral Neck Fractures | TERMINATED | NCT00757653 |
| ROCC Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00755144 |
| LCS Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00755144 |
| ROCC Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00755144 |
| LCS Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00755144 |
| Vanguard Knee System with PS Bearing | Other | Approved | Osteoarthritis | WITHDRAWN | NCT01308515 |
| Vanguard Knee System with AS Bearing | Other | Approved | Osteoarthritis | WITHDRAWN | NCT01308515 |
| Vanguard Knee System with conventional Instruments | Device | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT01092312 |
| Vanguard Knee System with Signature Knee Guide | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT01092312 |
| Vanguard Knee System with conventional Instruments | Device | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT01092312 |
| Vanguard Knee System with Signature Knee Guide | Other | Approved | Arthroplasty, Replacement, Knee | TERMINATED | NCT01092312 |
| Suture Wire | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01783483 |
| SternaLock Blue closure system | Other | Approved | Coronary Artery Disease | COMPLETED | NCT01783483 |
| Vanguard CR Single Cruciate Retaining Knee System | Other | Approved | Primary Osteoarthritis of Knee Nos | UNKNOWN | NCT03302013 |
| Vanguard XP Bi-cruciate Retaining Knee Replacement System | Other | Approved | Primary Osteoarthritis of Knee Nos | UNKNOWN | NCT03302013 |
| Vanguard CR Single Cruciate Retaining Knee System | Other | Approved | Primary Osteoarthritis of Knee Nos | UNKNOWN | NCT03302013 |
| Vanguard XP Bi-cruciate Retaining Knee Replacement System | Other | Approved | Primary Osteoarthritis of Knee Nos | UNKNOWN | NCT03302013 |
| Autologous Protein Solution "APS(TM)" | Other | Approved | Gonarthrosis | COMPLETED | NCT01773226 |
| Autologous Protein Solution "APS(TM)" | Other | Approved | Gonarthrosis | COMPLETED | NCT01773226 |
| Autologous Protein Solution "APS(TM)" | Other | Approved | Gonarthrosis | COMPLETED | NCT01773226 |
| Pedicle Screws | Other | Approved | Degeneration of Lumbar Intervertebral Disc | COMPLETED | NCT01549366 |
| Aspen Spinous Process Fixation Device | Device | Approved | Degeneration of Lumbar Intervertebral Disc | COMPLETED | NCT01549366 |
| Pedicle Screws | Other | Approved | Degeneration of Lumbar Intervertebral Disc | COMPLETED | NCT01549366 |
| Aspen Spinous Process Fixation Device | Device | Approved | Degeneration of Lumbar Intervertebral Disc | COMPLETED | NCT01549366 |
| Nobel Biocare Creos Cancellous Allograft | Other | Approved | Alveolar Bone Grafting | COMPLETED | NCT02444052 |
| Zimmer Puros Cancellous Allograft | Other | Approved | Alveolar Bone Grafting | COMPLETED | NCT02444052 |
| Uncemented acetabular cup without screw holes | Other | Approved | Arthroplasty Complications | COMPLETED | NCT03692351 |
| Uncemented acetabular cup with screw holes | Other | Approved | Arthroplasty Complications | COMPLETED | NCT03692351 |
| Avantage® Cup | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT02404727 |
| cup fixation | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT02404727 |
| Total Hip Arthroplasty | Other | Approved | Degenerative Joint Disease | COMPLETED | NCT01010763 |
| CLS Brevius stem with Kinectiv technology | Other | Preclinical | Osteoarthritis | TERMINATED | NCT03410940 |
| CLS Brevius stem with Kinectiv technology | Other | Preclinical | Osteoarthritis | TERMINATED | NCT03410940 |
| Synvisc-One | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03182374 |
| nSTRIDE APS | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03182374 |
| Trilogy AB Acetabular Hip Implant System | Other | Phase PHASE4 | Osteoarthritis | TERMINATED | NCT00715026 |
| Trilogy AB Acetabular Hip Implant System | Other | Phase PHASE4 | Osteoarthritis | TERMINATED | NCT00715026 |
| Taperloc | Other | Phase PHASE4 | Hip Osteoarthritis | COMPLETED | NCT02321683 |
| Taperloc | Other | Phase PHASE4 | Hip Osteoarthritis | COMPLETED | NCT02321683 |
| Total knee arthroplasty | Other | Phase PHASE4 | Unilateral Primary Osteoarthritis of Knee | COMPLETED | NCT01764984 |
| Total knee arthroplasty | Other | Phase PHASE4 | Unilateral Primary Osteoarthritis of Knee | COMPLETED | NCT01764984 |
| With PRP | Other | Approved | Burns | COMPLETED | NCT00858442 |
| With PRP | Other | Approved | Burns | COMPLETED | NCT00858442 |
| Copios | Other | Phase PHASE2 | Spondylolisthesis | TERMINATED | NCT01123850 |
| Copios | Other | Phase PHASE2 | Spondylolisthesis | TERMINATED | NCT01123850 |
| Puros® Dermis versus Alloderm® | Other | Approved | Gingival Recession | COMPLETED | NCT00881959 |
| Puros® Dermis versus Alloderm® | Other | Approved | Gingival Recession | COMPLETED | NCT00881959 |
| Bigliani/Flatow Shoulder System | Other | Preclinical | Osteoarthritis of Glenohumeral Joint | COMPLETED | NCT01488006 |
| Bigliani/Flatow Shoulder System | Other | Preclinical | Osteoarthritis of Glenohumeral Joint | COMPLETED | NCT01488006 |
| Wich prosthesis is used | Other | Approved | Osteoarthritis | UNKNOWN | NCT01966848 |
| Cemented femoral stem | Other | Approved | Hip Fractures | UNKNOWN | NCT02247791 |
| Uncemented femoral stem | Other | Approved | Hip Fractures | UNKNOWN | NCT02247791 |
| Cemented femoral stem | Other | Approved | Hip Fractures | UNKNOWN | NCT02247791 |
| Uncemented femoral stem | Other | Approved | Hip Fractures | UNKNOWN | NCT02247791 |
| Zimmer Gender Solutions PFJ Knee Prosthesis | Other | Preclinical | Arthritis | WITHDRAWN | NCT01469806 |
| Computer assist | Other | Phase PHASE4 | Knee Arthroplasty | TERMINATED | NCT00300326 |
| Computer assist | Other | Phase PHASE4 | Knee Arthroplasty | TERMINATED | NCT00300326 |
| Allogenix Plus | Other | Phase PHASE4 | Metopic Craniosynostosis | WITHDRAWN | NCT01006148 |
| knee arthroplasty, XLP polyethylene | Other | Preclinical | Arthroplasty, Replacement, Knee | UNKNOWN | NCT02178020 |
| knee arthroplasty, standard polyethylene | Other | Preclinical | Arthroplasty, Replacement, Knee | UNKNOWN | NCT02178020 |
| knee arthroplasty, XLP polyethylene | Other | Preclinical | Arthroplasty, Replacement, Knee | UNKNOWN | NCT02178020 |
| knee arthroplasty, standard polyethylene | Other | Preclinical | Arthroplasty, Replacement, Knee | UNKNOWN | NCT02178020 |
| Knee Replacement (with ROCC Knee prosthesis) | Other | Preclinical | Arthritis of Knee | TERMINATED | NCT00758901 |
| Knee Replacement (with ROCC Knee prosthesis) | Other | Preclinical | Arthritis of Knee | TERMINATED | NCT00758901 |
| Standard post-lobectomy wound care | Other | Approved | Lung Cancer | COMPLETED | NCT00665912 |
| Standard post-lobectomy wound care plus use of PRP and PPPc prepared by GPS and Plasmax respectively | Other | Approved | Lung Cancer | COMPLETED | NCT00665912 |
| Standard post-lobectomy wound care | Other | Approved | Lung Cancer | COMPLETED | NCT00665912 |
| Standard post-lobectomy wound care plus use of PRP and PPPc prepared by GPS and Plasmax respectively | Other | Approved | Lung Cancer | COMPLETED | NCT00665912 |
| Corticosteroid Injection | Other | Phase PHASE4 | Plantar Fasciitis | COMPLETED | NCT00758641 |
| L-PRP Injection | Other | Phase PHASE4 | Plantar Fasciitis | COMPLETED | NCT00758641 |
| Patient may be able to put weight on the operated leg | Other | Approved | Osteoarthritis | COMPLETED | NCT00179088 |
| Patient may be able to put weight on the operated leg | Other | Approved | Osteoarthritis | COMPLETED | NCT00179088 |
| Total hip arthroplasty (Fitmore or CLS uncemented femoral stem made by Zimmer-Biomet, Warshaw, USA) | Other | Approved | Primary Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03112785 |
| Total hip arthroplasty (Fitmore or CLS uncemented femoral stem made by Zimmer-Biomet, Warshaw, USA) | Other | Approved | Primary Hip Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03112785 |
| Discovery elbow minimally constrained | Other | Preclinical | Survivorship | TERMINATED | NCT01308463 |
| Hip replacement | Other | Approved | Osteoarthritis of Hip | UNKNOWN | NCT00551967 |
| Hip replacement | Other | Approved | Osteoarthritis of Hip | UNKNOWN | NCT00551967 |
| Total Hip Arthroplasty | Other | Approved | Osteoarthritis of Hip | UNKNOWN | NCT00545285 |
| Total Hip Arthroplasty | Other | Approved | Osteoarthritis of Hip | UNKNOWN | NCT00545285 |
| Placebo Injection with eccentric exercises | Other | Phase PHASE4 | Achilles Tendinopathy | COMPLETED | NCT00761423 |
| PRP Injection with eccentric exercises | Other | Phase PHASE4 | Achilles Tendinopathy | COMPLETED | NCT00761423 |
| Placebo Injection with eccentric exercises | Other | Phase PHASE4 | Achilles Tendinopathy | COMPLETED | NCT00761423 |
| PRP Injection with eccentric exercises | Other | Phase PHASE4 | Achilles Tendinopathy | COMPLETED | NCT00761423 |
| Corticosteroid Injection | Other | Approved | Pain | COMPLETED | NCT00757289 |
| PRP Injection | Other | Approved | Pain | COMPLETED | NCT00757289 |
| Corticosteroid Injection | Other | Approved | Pain | COMPLETED | NCT00757289 |
| PRP Injection | Other | Approved | Pain | COMPLETED | NCT00757289 |
| Oxford Unicompartmental Knee | Other | Approved | Knee Arthritis | COMPLETED | NCT00862316 |
| Oxford Unicompartmental Knee | Other | Approved | Knee Arthritis | COMPLETED | NCT00862316 |
| Vanguard CR Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763113 |
| Vanguard PS Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763113 |
| Vanguard CR Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763113 |
| Vanguard PS Knee | Other | Approved | Total Knee Arthroplasty | COMPLETED | NCT00763113 |
| Oxford Partial Knee | Other | Approved | Knee Arthroplasty | COMPLETED | NCT00759616 |
| Oxford Partial Knee | Other | Approved | Knee Arthroplasty | COMPLETED | NCT00759616 |
| Biomet SpinalPak® Non-Invasive Spine Fusion Stimulator | Other | Preclinical | Fusion of Spine (Disease) | TERMINATED | NCT01750840 |
| Biomet Orthopak® Non-Invasive Bone Growth Stimulator System | Other | Preclinical | Fusion of Spine (Disease) | TERMINATED | NCT01750840 |
| Biomet® EBI Bone Healing System | Other | Preclinical | Fusion of Spine (Disease) | TERMINATED | NCT01750840 |
| Biomet SpinalPak® Non-Invasive Spine Fusion Stimulator | Other | Preclinical | Fusion of Spine (Disease) | TERMINATED | NCT01750840 |
| Biomet Orthopak® Non-Invasive Bone Growth Stimulator System | Other | Preclinical | Fusion of Spine (Disease) | TERMINATED | NCT01750840 |
| Biomet® EBI Bone Healing System | Other | Preclinical | Fusion of Spine (Disease) | TERMINATED | NCT01750840 |
| Total Knee Replacement with Vanguard Total Knee | Other | Approved | Joint Disease | COMPLETED | NCT01256216 |
| Total Knee Replacement with Vanguard Total Knee | Other | Approved | Joint Disease | COMPLETED | NCT01256216 |
| ReCap Total Hip Resurfacing | Other | Preclinical | Arthritis | TERMINATED | NCT00758472 |
| ReCap Total Hip Resurfacing | Other | Preclinical | Arthritis | TERMINATED | NCT00758472 |
| ReCap Total Hip Resurfacing | Other | Preclinical | Osteoarthritis of the Hip | WITHDRAWN | NCT00758329 |
| ReCap Total Hip Resurfacing | Other | Preclinical | Osteoarthritis of the Hip | WITHDRAWN | NCT00758329 |
| Metal on Metal cementless hip | Other | Approved | Osteoarthritis | COMPLETED | NCT00757354 |
| Metal on Metal cementless hip | Other | Approved | Osteoarthritis | COMPLETED | NCT00757354 |
| Hip Fracture reduction Screw with HA Coating (Hiploc) | Other | Approved | Osteoarthritis | WITHDRAWN | NCT00756431 |
| Hip Fracture reduction Screw without HA Coating (Hiploc) | Other | Approved | Osteoarthritis | WITHDRAWN | NCT00756431 |
| Hip Fracture reduction Screw with HA Coating (Hiploc) | Other | Approved | Osteoarthritis | WITHDRAWN | NCT00756431 |
| Hip Fracture reduction Screw without HA Coating (Hiploc) | Other | Approved | Osteoarthritis | WITHDRAWN | NCT00756431 |
| Vanguard Knee System with PS Bearing | Other | Approved | Osteoarthritis | WITHDRAWN | NCT01308515 |
| Vanguard Knee System with AS Bearing | Other | Approved | Osteoarthritis | WITHDRAWN | NCT01308515 |
| Metal-on-Metal | Other | Approved | Osteoarthritis | TERMINATED | NCT01247038 |
| Metal on ceramic articulation | Other | Approved | Osteoarthritis | TERMINATED | NCT01247038 |
| Metal-on-Metal | Other | Approved | Osteoarthritis | TERMINATED | NCT01247038 |
| Metal on ceramic articulation | Other | Approved | Osteoarthritis | TERMINATED | NCT01247038 |
| Pediatric Locking Nail | Other | Preclinical | Femur Fracture | COMPLETED | NCT00725894 |
| Pediatric Locking Nail | Other | Preclinical | Femur Fracture | COMPLETED | NCT00725894 |
| Cobalt™ Bone Cement | Other | Preclinical | Osteoarthritis | WITHDRAWN | NCT00589485 |
| Simplex® Bone Cement | Other | Preclinical | Osteoarthritis | WITHDRAWN | NCT00589485 |
| Surgery | Procedure | Approved | Nonunion of Fracture of Fifth Metatarsal | TERMINATED | NCT00586170 |
| Placebo Device | Device | Approved | Nonunion of Fracture of Fifth Metatarsal | TERMINATED | NCT00586170 |
| EBI Bone Healing System | Other | Approved | Nonunion of Fracture of Fifth Metatarsal | TERMINATED | NCT00586170 |
| Surgery | Procedure | Approved | Nonunion of Fracture of Fifth Metatarsal | TERMINATED | NCT00586170 |
| Placebo Device | Device | Approved | Nonunion of Fracture of Fifth Metatarsal | TERMINATED | NCT00586170 |
| EBI Bone Healing System | Other | Approved | Nonunion of Fracture of Fifth Metatarsal | TERMINATED | NCT00586170 |
| ChonDux | Other | Approved | Cartilage Defect | TERMINATED | NCT01110070 |
| ChonDux | Other | Approved | Cartilage Defect | TERMINATED | NCT01110070 |
| BiHapro hip stem with PPS Ti+BoneMaster HA | Other | Preclinical | Osteoarthritis | TERMINATED | NCT00755001 |
| BiHapro hip stem with PPS Ti+Plasma HA | Other | Preclinical | Osteoarthritis | TERMINATED | NCT00755001 |
| BiHapro hip stem with PPS Ti+BoneMaster HA | Other | Preclinical | Osteoarthritis | TERMINATED | NCT00755001 |
| BiHapro hip stem with PPS Ti+Plasma HA | Other | Preclinical | Osteoarthritis | TERMINATED | NCT00755001 |
| Signature Custom Guides | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT01410786 |
| Conventional Instrumentation | Device | Approved | Osteoarthritis, Knee | COMPLETED | NCT01410786 |
| Signature Custom Guides | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT01410786 |
| Conventional Instrumentation | Device | Approved | Osteoarthritis, Knee | COMPLETED | NCT01410786 |
| Computer Assisted Navigation | Other | Approved | Joint Disease | COMPLETED | NCT01145157 |
| Conventional Instrumentation | Device | Approved | Joint Disease | COMPLETED | NCT01145157 |
| Signature Knee Guide | Other | Approved | Joint Disease | COMPLETED | NCT01145157 |
| Computer Assisted Navigation | Other | Approved | Joint Disease | COMPLETED | NCT01145157 |
| Conventional Instrumentation | Device | Approved | Joint Disease | COMPLETED | NCT01145157 |
| Signature Knee Guide | Other | Approved | Joint Disease | COMPLETED | NCT01145157 |
| RSA images | Other | Approved | Radiostereometric Analysis | UNKNOWN | NCT01754155 |
| RSA images | Other | Approved | Radiostereometric Analysis | UNKNOWN | NCT01754155 |
| Cementless Oxford Partial Knee | Other | Preclinical | Arthroplasty, Replacement, Knee | WITHDRAWN | NCT00760188 |
| Cementless Oxford Partial Knee | Other | Preclinical | Arthroplasty, Replacement, Knee | WITHDRAWN | NCT00760188 |
| Cementless Oxford Partial Knee | Other | Preclinical | Arthroplasty, Replacement, Knee | WITHDRAWN | NCT00760188 |
| BOLD-MRI | Other | Approved | Peripheral Arterial Disease | COMPLETED | NCT02601430 |
| Lipofilling of the midface | Other | Phase PHASE2 | Lipofilling | COMPLETED | NCT01461785 |
| Addition of PRP ( platelet rich plasma) to the lipograft | Other | Phase PHASE2 | Lipofilling | COMPLETED | NCT01461785 |
| Lipofilling of the midface | Other | Phase PHASE2 | Lipofilling | COMPLETED | NCT01461785 |
| Addition of PRP ( platelet rich plasma) to the lipograft | Other | Phase PHASE2 | Lipofilling | COMPLETED | NCT01461785 |
| Trabecular Metal Modular Cup | Other | Approved | Revision, Joint | COMPLETED | NCT01183260 |
| Trabecular Metal Revision Cup | Other | Approved | Revision, Joint | COMPLETED | NCT01183260 |
| 28 mm CrCo head, Trilogy CH cup, VerSys Fiber stem,Zimmer) | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| Bimetric stem, mallory/head cup, 28 mm ceramic head, Biomet | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| ReCap/Magnum modular head, Biomet | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| articular surface replacement ASR, DePuy | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| 28 mm CrCo head, Trilogy CH cup, VerSys Fiber stem,Zimmer) | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| Bimetric stem, mallory/head cup, 28 mm ceramic head, Biomet | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| ReCap/Magnum modular head, Biomet | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| articular surface replacement ASR, DePuy | Other | Phase PHASE2 | Osteoarthritis, Hip | UNKNOWN | NCT01113762 |
| Leukocyte- and Platelet-Rich Plasma (L-PRP) | Other | Preclinical | Lateral Epicondylitis | TERMINATED | NCT02588040 |
| Leukocyte- and Platelet-Rich Plasma (L-PRP) | Other | Preclinical | Lateral Epicondylitis | TERMINATED | NCT02588040 |
| ReCap Total Hip Resurfacing | Other | Approved | Arthritis | COMPLETED | NCT00750984 |
| Posterior approach | Other | Approved | Arthritis | COMPLETED | NCT00750984 |
| Anterolateral approach | Other | Approved | Arthritis | COMPLETED | NCT00750984 |
| ReCap Total Hip Resurfacing | Other | Approved | Arthritis | COMPLETED | NCT00750984 |
| Posterior approach | Other | Approved | Arthritis | COMPLETED | NCT00750984 |
| Anterolateral approach | Other | Approved | Arthritis | COMPLETED | NCT00750984 |
| Wire Cerclage | Other | Approved | Sternal Fracture | COMPLETED | NCT02686099 |
| SternaLock 360 | Other | Approved | Sternal Fracture | COMPLETED | NCT02686099 |
| Wire Cerclage | Other | Approved | Sternal Fracture | COMPLETED | NCT02686099 |
| SternaLock 360 | Other | Approved | Sternal Fracture | COMPLETED | NCT02686099 |
| wire (control) | Other | Approved | Sternal Wound Infection | COMPLETED | NCT00819286 |
| SternaLock Rigid Fixation Plates | Other | Approved | Sternal Wound Infection | COMPLETED | NCT00819286 |
| wire (control) | Other | Approved | Sternal Wound Infection | COMPLETED | NCT00819286 |
| SternaLock Rigid Fixation Plates | Other | Approved | Sternal Wound Infection | COMPLETED | NCT00819286 |
| Nobel Biocare Creos Cancellous Allograft | Other | Approved | Alveolar Bone Grafting | COMPLETED | NCT02444052 |
| Zimmer Puros Cancellous Allograft | Other | Approved | Alveolar Bone Grafting | COMPLETED | NCT02444052 |
| there is no intervention | Other | Preclinical | Total Knee Arthroplasty / Position of Customized X-Ray PSI Guides Using Optical Navigation | COMPLETED | NCT02504112 |
| there is no intervention | Other | Preclinical | Total Knee Arthroplasty / Position of Customized X-Ray PSI Guides Using Optical Navigation | COMPLETED | NCT02504112 |
| Vanguard High Flex RP | Other | Approved | Osteoarthritis | COMPLETED | NCT01010269 |
| Vanguard Complete Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT01010269 |
| Instrument | Device | Approved | Osteoarthritis of the Knee | COMPLETED | NCT01072019 |
| Instrument | Device | Approved | Osteoarthritis of the Knee | COMPLETED | NCT01072019 |
| VerSys Beaded FullCoat, Zimmer | Other | Approved | Femoral Neck Fracture | COMPLETED | NCT01114646 |
| Cemented Hip Hemiarthroplasty | Other | Approved | Femoral Neck Fracture | COMPLETED | NCT01114646 |
| VerSys Beaded FullCoat, Zimmer | Other | Approved | Femoral Neck Fracture | COMPLETED | NCT01114646 |
| Cemented Hip Hemiarthroplasty | Other | Approved | Femoral Neck Fracture | COMPLETED | NCT01114646 |
| Avantage® Cup | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT02404727 |
| cup fixation | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT02404727 |
| Avantage® Cup | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT02404727 |
| cup fixation | Other | Approved | Osteoarthritis, Hip | COMPLETED | NCT02404727 |
| Total Shoulder Arthroplasty | Other | Approved | Arthritis | TERMINATED | NCT01884077 |
| Reverse Shoulder Arthroplasty | Other | Approved | Arthritis | TERMINATED | NCT01884077 |
| Total Shoulder Arthroplasty | Other | Approved | Arthritis | TERMINATED | NCT01884077 |
| Reverse Shoulder Arthroplasty | Other | Approved | Arthritis | TERMINATED | NCT01884077 |
| Aspen Spinous Process Fixation Device | Device | Preclinical | Spondylolisthesis | TERMINATED | NCT01560273 |
| Zimmer Gender(R) Solutions(TM) Natural-Knee(R) Flex System | Other | Preclinical | Osteoarthritis | WITHDRAWN | NCT01463566 |
| Zimmer Gender(R) Solutions(TM) Natural-Knee(R) Flex System | Other | Preclinical | Osteoarthritis | WITHDRAWN | NCT01463566 |
| OsseoFit™ Porous Tissue Matrix™ | Other | Approved | Bone Graft | WITHDRAWN | NCT00708474 |
| OsseoFit™ Porous Tissue Matrix™ | Other | Approved | Bone Graft | WITHDRAWN | NCT00708474 |
| OsseoFit™ Porous Tissue Matrix™ | Other | Approved | Bone Graft | WITHDRAWN | NCT00708474 |
| Pedicle Screw Fixation | Other | Approved | Degenerative Disc Disease | WITHDRAWN | NCT01016314 |
| Aspen Spinous Process System | Other | Approved | Degenerative Disc Disease | WITHDRAWN | NCT01016314 |
| Pedicle Screw Fixation | Other | Approved | Degenerative Disc Disease | WITHDRAWN | NCT01016314 |
| Aspen Spinous Process System | Other | Approved | Degenerative Disc Disease | WITHDRAWN | NCT01016314 |
| TM- Ardis implant and Metal Reduction CT software | Other | Preclinical | Degenerative Disc Disease | WITHDRAWN | NCT02170558 |
| TM- Ardis implant and Metal Reduction CT software | Other | Preclinical | Degenerative Disc Disease | WITHDRAWN | NCT02170558 |
| OsteoGen | Other | Preclinical | Tibia Fracture Non Union Bone | TERMINATED | NCT00726193 |
| OsteoGen | Other | Preclinical | Tibia Fracture Non Union Bone | TERMINATED | NCT00726193 |
| OsteoGen | Other | Preclinical | Tibia Fracture Non Union Bone | TERMINATED | NCT00726193 |
| Standard polyethylene acetabular component | Other | Approved | Total Hip Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02254980 |
| Vitamin-E diffused polyethylene acetabular component | Other | Approved | Total Hip Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02254980 |
| Standard polyethylene acetabular component | Other | Approved | Total Hip Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02254980 |
| Vitamin-E diffused polyethylene acetabular component | Other | Approved | Total Hip Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02254980 |
| Standard polyethylene acetabular component | Other | Approved | Total Hip Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02254980 |
| Vitamin-E diffused polyethylene acetabular component | Other | Approved | Total Hip Arthroplasty | ACTIVE_NOT_RECRUITING | NCT02254980 |
| ReCap Total Hip Resurfacing System | Other | Approved | Arthritis | COMPLETED | NCT00604734 |
| ReCap Total Hip Resurfacing System | Other | Approved | Arthritis | COMPLETED | NCT00604734 |
| APS | Other | Phase PHASE1 | Osteoarthritis, Knee | COMPLETED | NCT02262364 |
| APS | Other | Phase PHASE1 | Osteoarthritis, Knee | COMPLETED | NCT02262364 |
| Plasma Coated Acetabular Shell | Other | Approved | Arthropathy of Hip | COMPLETED | NCT00859976 |
| BoneMaster coated acetabular shell. | Other | Approved | Arthropathy of Hip | COMPLETED | NCT00859976 |
| Plasma Coated Acetabular Shell | Other | Approved | Arthropathy of Hip | COMPLETED | NCT00859976 |
| BoneMaster coated acetabular shell. | Other | Approved | Arthropathy of Hip | COMPLETED | NCT00859976 |
| Slotted hole C-Tek™ Plate | Other | Approved | Herniated Disc | TERMINATED | NCT00585923 |
| Fixed hole C-Tek™ Plate | Other | Approved | Herniated Disc | TERMINATED | NCT00585923 |
| Slotted hole C-Tek™ Plate | Other | Approved | Herniated Disc | TERMINATED | NCT00585923 |
| Fixed hole C-Tek™ Plate | Other | Approved | Herniated Disc | TERMINATED | NCT00585923 |
| TM-Ardis Interbody | Other | Phase PHASE4 | Degenerative Disc Disease | COMPLETED | NCT02429908 |
| TM-Ardis Interbody | Other | Phase PHASE4 | Degenerative Disc Disease | COMPLETED | NCT02429908 |
| Cellentra VCBM | Other | Approved | Cervical Disc Degenerative Disorder | COMPLETED | NCT02182843 |
| Cellentra VCBM | Other | Approved | Cervical Disc Degenerative Disorder | COMPLETED | NCT02182843 |
| Cellentra VCBM | Other | Approved | Cervical Disc Degenerative Disorder | COMPLETED | NCT02182843 |
| Exceed ABT | Other | Approved | Osteoarthritis Arthritis | COMPLETED | NCT02340390 |
| Exceed ABT | Other | Approved | Osteoarthritis Arthritis | COMPLETED | NCT02340390 |
| Trabecular Metal Humeral Stem | Other | Preclinical | Osteoarthritis | TERMINATED | NCT01480453 |
| Trabecular Metal Humeral Stem | Other | Preclinical | Osteoarthritis | TERMINATED | NCT01480453 |
| Trabecular Metal Humeral Stem | Other | Preclinical | Osteoarthritis | TERMINATED | NCT01480453 |
| Trabecular Metal Humeral Stem | Other | Preclinical | Osteoarthritis | TERMINATED | NCT01480453 |
| Incision technique | Other | Approved | Gonarthrosis Patients Who Need Artificial Knee Joint Total Replacement | COMPLETED | NCT01010828 |
| Incision technique | Other | Approved | Gonarthrosis Patients Who Need Artificial Knee Joint Total Replacement | COMPLETED | NCT01010828 |
| Incision technique | Other | Approved | Gonarthrosis Patients Who Need Artificial Knee Joint Total Replacement | COMPLETED | NCT01010828 |
| Sternal Wires | Other | Approved | Cardiac Surgery | COMPLETED | NCT03282578 |
| Sternalock 360 sternal plating system | Other | Approved | Cardiac Surgery | COMPLETED | NCT03282578 |
| Sternal Wires | Other | Approved | Cardiac Surgery | COMPLETED | NCT03282578 |
| Sternalock 360 sternal plating system | Other | Approved | Cardiac Surgery | COMPLETED | NCT03282578 |
| Sternal Wires | Other | Approved | Cardiac Surgery | COMPLETED | NCT03282578 |
| Sternalock 360 sternal plating system | Other | Approved | Cardiac Surgery | COMPLETED | NCT03282578 |
| COMPREHENSIVE | Other | Preclinical | Rotator Cuff Tear Arthropathy | COMPLETED | NCT02084693 |
| COMPREHENSIVE | Other | Preclinical | Rotator Cuff Tear Arthropathy | COMPLETED | NCT02084693 |
| Shared Decision Making Tool | Other | Approved | Knee Osteoarthritis | TERMINATED | NCT04011488 |
| Sidus Stem-Free Total Shoulder Arthroplasty System | Other | Approved | Osteoarthritis | COMPLETED | NCT01878253 |
| Sidus Stem-Free Total Shoulder Arthroplasty System | Other | Approved | Osteoarthritis | COMPLETED | NCT01878253 |
| shoulder x-ray | Other | Preclinical | Shoulder Arthritis | COMPLETED | NCT03148184 |
| Conventional | Other | Approved | Gonarthrosis | COMPLETED | NCT04114201 |
| PSI | Other | Approved | Gonarthrosis | COMPLETED | NCT04114201 |
| Conventional | Other | Approved | Gonarthrosis | COMPLETED | NCT04114201 |
| PSI | Other | Approved | Gonarthrosis | COMPLETED | NCT04114201 |
| Stated-Preferences Evaluation Instrument | Device | Preclinical | Arthritis | COMPLETED | NCT03058380 |
| Surgery | Procedure | Preclinical | Spinal Deformity | COMPLETED | NCT01220505 |
| Surgery | Procedure | Preclinical | Spinal Deformity | COMPLETED | NCT01220505 |
| Taperloc Complete Standard | Other | Approved | Osteoarthritis | COMPLETED | NCT02087436 |
| Taperloc Complete Microplasty | Other | Approved | Osteoarthritis | COMPLETED | NCT02087436 |
| Taperloc Complete Standard | Other | Approved | Osteoarthritis | COMPLETED | NCT02087436 |
| Taperloc Complete Microplasty | Other | Approved | Osteoarthritis | COMPLETED | NCT02087436 |
| Nano | Other | Approved | Joint Disease | COMPLETED | NCT01936259 |
| Mini Stem | Other | Approved | Joint Disease | COMPLETED | NCT01936259 |
| Nano | Other | Approved | Joint Disease | COMPLETED | NCT01936259 |
| Mini Stem | Other | Approved | Joint Disease | COMPLETED | NCT01936259 |
| Bactisure | Other | Preclinical | Infection of Total Knee Joint Prosthesis | COMPLETED | NCT03192124 |
| Bactisure | Other | Preclinical | Infection of Total Knee Joint Prosthesis | COMPLETED | NCT03192124 |
| Dynesys Spinal System | Other | Approved | Degenerative Spondylolisthesis | TERMINATED | NCT01528072 |
| NexGen PS Knee Prosthesis by Zimmer | Other | Approved | Osteoarthritis Arthritis | COMPLETED | NCT02269254 |
| Persona PS Knee Prosthesis by Zimmer | Other | Approved | Osteoarthritis Arthritis | COMPLETED | NCT02269254 |
| NexGen PS Knee Prosthesis by Zimmer | Other | Approved | Osteoarthritis Arthritis | COMPLETED | NCT02269254 |
| Persona PS Knee Prosthesis by Zimmer | Other | Approved | Osteoarthritis Arthritis | COMPLETED | NCT02269254 |
| KneeAlign 2 | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02695329 |
| KneeAlign 2 | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02695329 |
| KneeAlign 2 | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02695329 |
| KneeAlign 2 | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02695329 |
| SpineLink® , SpineLink® II | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT00726310 |
| SpineLink® , SpineLink® II | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT00726310 |
| SpineLink® , SpineLink® II | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT00726310 |
| Acetabular Liner | Other | Approved | Hip Osteoarthritis | TERMINATED | NCT01883492 |
| Acetabular Cup | Other | Approved | Hip Osteoarthritis | TERMINATED | NCT01883492 |
| Femoral Stem | Other | Approved | Hip Osteoarthritis | TERMINATED | NCT01883492 |
| Primary TKA with uncemented trabecular metal | Other | Approved | Knee Osteoarthritis | UNKNOWN | NCT03970460 |
| Primary TKA with cemented modular metal-backed tibial implant | Other | Approved | Knee Osteoarthritis | UNKNOWN | NCT03970460 |
| Primary TKA with uncemented trabecular metal | Other | Approved | Knee Osteoarthritis | UNKNOWN | NCT03970460 |
| Primary TKA with cemented modular metal-backed tibial implant | Other | Approved | Knee Osteoarthritis | UNKNOWN | NCT03970460 |
| VueLock™ Anterior Cervical Plate | Other | Preclinical | Trauma | COMPLETED | NCT00726128 |
| VueLock™ Anterior Cervical Plate | Other | Preclinical | Trauma | COMPLETED | NCT00726128 |
| Echo Bi-Metric | Other | Approved | Osteoarthritis, Hip | UNKNOWN | NCT02656771 |
| Echo Bi-Metric | Other | Approved | Osteoarthritis, Hip | UNKNOWN | NCT02656771 |
| Bone marrow concentration device | Device | Preclinical | Peripheral Arterial Disease | NO_LONGER_AVAILABLE | NCT02474121 |
| Standard Surgery | Procedure | Approved | Hip Arthroplasty | COMPLETED | NCT00261040 |
| Minimally Invasive Surgery | Procedure | Approved | Hip Arthroplasty | COMPLETED | NCT00261040 |
| Standard Surgery | Procedure | Approved | Hip Arthroplasty | COMPLETED | NCT00261040 |
| Minimally Invasive Surgery | Procedure | Approved | Hip Arthroplasty | COMPLETED | NCT00261040 |
| APS | Other | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT02580643 |
| APS | Other | Preclinical | Osteoarthritis, Knee | COMPLETED | NCT02580643 |
| nSTRIDE Autologous Protein Solution (APS) Kit | Other | Approved | Patellofemoral Osteoarthritis | COMPLETED | NCT02610192 |
| nSTRIDE Autologous Protein Solution (APS) Kit | Other | Approved | Patellofemoral Osteoarthritis | COMPLETED | NCT02610192 |
| Patients who received the Stafit Acetabular System | Other | Preclinical | Osteoarthritis, Hip | TERMINATED | NCT04079114 |
| Patients who received the Stafit Acetabular System | Other | Preclinical | Osteoarthritis, Hip | TERMINATED | NCT04079114 |
| iAssist Knee | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03227692 |
| Total Knee Arthroplasty | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03227692 |
| Persona Knee System | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03227692 |
| iAssist Knee | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03227692 |
| Total Knee Arthroplasty | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03227692 |
| Persona Knee System | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03227692 |
| The Spinal Tethering System | Other | Preclinical | Adolescent Idiopathic Scoliosis | UNKNOWN | NCT02897453 |
| RibFix Advantage | Other | Preclinical | Rib Fracture Multiple | WITHDRAWN | NCT04163224 |
| RibFix Advantage | Other | Preclinical | Rib Fracture Multiple | WITHDRAWN | NCT04163224 |
| Anterior Support Screw | Other | Approved | Trochanteric Fracture of Femur | COMPLETED | NCT03196193 |
| ZNN CM Asia | Other | Approved | Trochanteric Fracture of Femur | COMPLETED | NCT03196193 |
| Open Reduction and Internal Fixation | Other | Approved | Trochanteric Fracture of Femur | COMPLETED | NCT03196193 |
| Anterior Support Screw | Other | Approved | Trochanteric Fracture of Femur | COMPLETED | NCT03196193 |
| ZNN CM Asia | Other | Approved | Trochanteric Fracture of Femur | COMPLETED | NCT03196193 |
| Open Reduction and Internal Fixation | Other | Approved | Trochanteric Fracture of Femur | COMPLETED | NCT03196193 |
| Transfusion of washed autolgous RBCs | Other | Phase PHASE4 | Erythrocyte Transfusion | TERMINATED | NCT03089047 |
| Transfusion of rejuvenated and washed autolgous RBCs | Other | Phase PHASE4 | Erythrocyte Transfusion | TERMINATED | NCT03089047 |
| Saline | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02138890 |
| APS | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02138890 |
| Saline | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02138890 |
| APS | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT02138890 |
| Total hip arthroplasty | Other | Preclinical | Degenerative Joint Disease of Hip | TERMINATED | NCT04348968 |
| Total hip arthroplasty | Other | Preclinical | Degenerative Joint Disease of Hip | TERMINATED | NCT04348968 |
| Total hip arthroplasty | Other | Preclinical | Degenerative Joint Disease of Hip | TERMINATED | NCT04348968 |
| Conventional Instrumentation | Device | Approved | Osteoarthritis | TERMINATED | NCT01763684 |
| Signature Custom Guides | Other | Approved | Osteoarthritis | TERMINATED | NCT01763684 |
| Conventional Instrumentation | Device | Approved | Osteoarthritis | TERMINATED | NCT01763684 |
| Signature Custom Guides | Other | Approved | Osteoarthritis | TERMINATED | NCT01763684 |
| Sidus Stem-Free Shoulder | Other | Approved | Osteoarthritis | WITHDRAWN | NCT04063943 |
| Sidus Stem-Free Shoulder | Other | Approved | Osteoarthritis | WITHDRAWN | NCT04063943 |
| Patients who met the inclusion/exclusion criteria to receive the Avenir Müller stem. | Other | Preclinical | Osteoarthritis, Hip | COMPLETED | NCT04079127 |
| Patients who met the inclusion/exclusion criteria to receive the Avenir Müller stem. | Other | Preclinical | Osteoarthritis, Hip | COMPLETED | NCT04079127 |
| Placebo procedure (sham) | Procedure | Approved | Critical Limb Ischemia | TERMINATED | NCT01049919 |
| Bone marrow concentration device | Device | Approved | Critical Limb Ischemia | TERMINATED | NCT01049919 |
| Placebo procedure (sham) | Procedure | Approved | Critical Limb Ischemia | TERMINATED | NCT01049919 |
| Bone marrow concentration device | Device | Approved | Critical Limb Ischemia | TERMINATED | NCT01049919 |
| Placebo procedure (sham) | Procedure | Approved | Critical Limb Ischemia | TERMINATED | NCT01049919 |
| Bone marrow concentration device | Device | Approved | Critical Limb Ischemia | TERMINATED | NCT01049919 |
| Magnetic Resonance Imaging (MRI) | Other | Preclinical | Developmental Dysplasia of the Hip | UNKNOWN | NCT02185365 |
| OmniMax MMF system | Other | Preclinical | Mandibular Fractures | COMPLETED | NCT03075865 |
| OmniMax MMF system | Other | Preclinical | Mandibular Fractures | COMPLETED | NCT03075865 |
| SternaLock Blu | Other | Preclinical | Cardiac Surgical Procedures | TERMINATED | NCT03709693 |
| SternaLock Blu | Other | Preclinical | Cardiac Surgical Procedures | TERMINATED | NCT03709693 |
| SternaLock Blu | Other | Preclinical | Cardiac Surgical Procedures | TERMINATED | NCT03709693 |
| Robot-assisted intracerebral catheter | Other | Approved | Intracerebral Hematoma | WITHDRAWN | NCT03414307 |
| Intracerebral catheter placement | Other | Approved | Intracerebral Hematoma | WITHDRAWN | NCT03414307 |
| Zimmer MotionLoc Screw | Other | Preclinical | Distal Tibia Fractures | COMPLETED | NCT02717546 |
| Zimmer MotionLoc Screw | Other | Preclinical | Distal Tibia Fractures | COMPLETED | NCT02717546 |
| Zimmer MotionLoc Screw | Other | Preclinical | Distal Tibia Fractures | COMPLETED | NCT02717546 |
| MUVR | Other | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT05006274 |
| Verasense technology | Other | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT05006274 |
| Persona Trabecular Metal Tibia | Other | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT05006274 |
| MUVR | Other | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT05006274 |
| Verasense technology | Other | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT05006274 |
| Persona Trabecular Metal Tibia | Other | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT05006274 |
| Trabecular Metal Monoblock Tibial Total Knee Component | Other | Phase PHASE4 | Osteoarthritis | COMPLETED | NCT01180595 |
| Trabecular Metal Modular Tibial Total Knee Component | Other | Phase PHASE4 | Osteoarthritis | COMPLETED | NCT01180595 |
| LPS Flex Porous Femoral Components | Other | Preclinical | Osteoarthritis | WITHDRAWN | NCT01462240 |
| LPS Flex Porous Femoral Components | Other | Preclinical | Osteoarthritis | WITHDRAWN | NCT01462240 |
| Subchondroplasty | Other | Preclinical | Bone Marrow Edema | COMPLETED | NCT01621893 |
| Subchondroplasty | Other | Preclinical | Bone Marrow Edema | COMPLETED | NCT01621893 |
| Zimmer-Biomet Posterior Stabilizing total knee arthroplasty | Other | Preclinical | Arthroplasty, Replacement, Knee | COMPLETED | NCT04103515 |
| Zimmer-Biomet Posterior Cruciate Retaining total knee arthroplasty | Other | Preclinical | Arthroplasty, Replacement, Knee | COMPLETED | NCT04103515 |
| Zimmer-Biomet Posterior Stabilizing total knee arthroplasty | Other | Preclinical | Arthroplasty, Replacement, Knee | COMPLETED | NCT04103515 |
| Zimmer-Biomet Posterior Cruciate Retaining total knee arthroplasty | Other | Preclinical | Arthroplasty, Replacement, Knee | COMPLETED | NCT04103515 |
| Zimmer-Biomet Posterior Stabilizing total knee arthroplasty | Other | Preclinical | Arthroplasty, Replacement, Knee | COMPLETED | NCT04103515 |
| Zimmer-Biomet Posterior Cruciate Retaining total knee arthroplasty | Other | Preclinical | Arthroplasty, Replacement, Knee | COMPLETED | NCT04103515 |
| TESS V2 | Other | Preclinical | Osteoarthritis Shoulder | COMPLETED | NCT03431857 |
| TESS V2 | Other | Preclinical | Osteoarthritis Shoulder | COMPLETED | NCT03431857 |
| TESS V2 | Other | Preclinical | Osteoarthritis Shoulder | COMPLETED | NCT03431857 |
| BioCUE Platelet Concentration System | Other | Preclinical | Avascular Necrosis of the Femoral Head | UNKNOWN | NCT02662881 |
| PerFuse Percutaneous Decompression System | Other | Preclinical | Avascular Necrosis of the Femoral Head | UNKNOWN | NCT02662881 |
| BioCUE Platelet Concentration System | Other | Preclinical | Avascular Necrosis of the Femoral Head | UNKNOWN | NCT02662881 |
| PerFuse Percutaneous Decompression System | Other | Preclinical | Avascular Necrosis of the Femoral Head | UNKNOWN | NCT02662881 |
| HealthLoop mobile application | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT03481595 |
| HealthLoop mobile application | Other | Approved | Arthroplasty, Replacement, Knee | COMPLETED | NCT03481595 |
| JuggerKnot Mini Soft Anchor | Other | Preclinical | TMJ Disc Disorder | WITHDRAWN | NCT04033692 |
| G7 PPS Acetabular Component | Other | Approved | Osteoarthritis | COMPLETED | NCT02447653 |
| G7 HA Acetabular Component | Other | Approved | Osteoarthritis | COMPLETED | NCT02447653 |
| G7 PPS Acetabular Component | Other | Approved | Osteoarthritis | COMPLETED | NCT02447653 |
| G7 HA Acetabular Component | Other | Approved | Osteoarthritis | COMPLETED | NCT02447653 |
| CT Scan | Other | Preclinical | Osteo Arthritis Shoulders | COMPLETED | NCT03151109 |
| CT Scan | Other | Preclinical | Osteo Arthritis Shoulders | COMPLETED | NCT03151109 |
| CR polyethylene bearing | Other | Approved | Knee Osteoarthritis | COMPLETED | NCT03568123 |
| MC polyethylene bearing | Other | Approved | Knee Osteoarthritis | COMPLETED | NCT03568123 |
| CR polyethylene bearing | Other | Approved | Knee Osteoarthritis | COMPLETED | NCT03568123 |
| MC polyethylene bearing | Other | Approved | Knee Osteoarthritis | COMPLETED | NCT03568123 |
| Zimmer NexGen® Trabecular Metal Technology (TMT), Modular | Other | Approved | Arthrosis of the Knee | ACTIVE_NOT_RECRUITING | NCT01637051 |
| Zimmer NexGen® Trabecular Metal Technology (TMT), Monoblock | Other | Approved | Arthrosis of the Knee | ACTIVE_NOT_RECRUITING | NCT01637051 |
| Zimmer NexGen® Trabecular Metal Technology (TMT), Modular | Other | Approved | Arthrosis of the Knee | ACTIVE_NOT_RECRUITING | NCT01637051 |
| Zimmer NexGen® Trabecular Metal Technology (TMT), Monoblock | Other | Approved | Arthrosis of the Knee | ACTIVE_NOT_RECRUITING | NCT01637051 |
| Tourniquet | Other | Approved | Osteoarthritis, Knee | UNKNOWN | NCT03666598 |
| THP Hip Fracture Plating System with telescoping lag screws | Other | Approved | Femur Fracture | TERMINATED | NCT03870477 |
| THP Hip Fracture Plating System with telescoping lag screws | Other | Approved | Femur Fracture | TERMINATED | NCT03870477 |
| PERSONA Total Knee | Other | Approved | Knee Pain | TERMINATED | NCT03970629 |
| N-Force Screws Augmented with N-Force Blue | Other | Approved | Intracapsular Proximal Femur Fracture | TERMINATED | NCT03807349 |
| BioWick SureLock Implant | Other | Approved | Rotator Cuff Tear | COMPLETED | NCT03199391 |
| BioWick SureLock Implant | Other | Approved | Rotator Cuff Tear | COMPLETED | NCT03199391 |
| BioWick SureLock Implant | Other | Approved | Rotator Cuff Tear | COMPLETED | NCT03199391 |
| Taperloc Complete Reduced Distal stem | Other | Approved | Hip Osteoarthritis | COMPLETED | NCT03409666 |
| Taperloc Complete Microplasty stem | Other | Approved | Hip Osteoarthritis | COMPLETED | NCT03409666 |
| Taperloc Complete Reduced Distal stem | Other | Approved | Hip Osteoarthritis | COMPLETED | NCT03409666 |
| Taperloc Complete Microplasty stem | Other | Approved | Hip Osteoarthritis | COMPLETED | NCT03409666 |
| Vanguard with E1 PS Bearing | Other | Preclinical | Varus Deformity | TERMINATED | NCT02088372 |
| Vanguard with E1 PS Bearing | Other | Preclinical | Varus Deformity | TERMINATED | NCT02088372 |
| Posterior Lateral Approach Total Hip Arthroplasty | Other | Approved | Noninflammatory Degenerative Joint Disease | TERMINATED | NCT02220478 |
| Posterior Lateral Approach Total Hip Arthroplasty | Other | Approved | Noninflammatory Degenerative Joint Disease | TERMINATED | NCT02220478 |
| Medial Congruent Polyethylene (MC) | Other | Approved | Osteoarthritis, Knee | UNKNOWN | NCT03494348 |
| Medial Congruent Polyethylene (MC) | Other | Approved | Osteoarthritis, Knee | UNKNOWN | NCT03494348 |
| Surgical approach (ReCap Hip Resurfacing System) | Other | Approved | Osteonecrosis | COMPLETED | NCT00913679 |
| Surgical approach (ReCap Hip Resurfacing System) | Other | Approved | Osteonecrosis | COMPLETED | NCT00913679 |
| Osteopal G vs. Refobacin-Palacos R bone cement | Other | Approved | Osteoarthritis | WITHDRAWN | NCT00175162 |
| Tibial component | Other | Approved | Osteoarthritis | COMPLETED | NCT00138853 |
| Crown lengthening/gingivectomy | Other | Approved | Gummy Smile | UNKNOWN | NCT05616715 |
| Peek device | Device | Approved | Gummy Smile | UNKNOWN | NCT05616715 |
| Crown lengthening/gingivectomy | Other | Approved | Gummy Smile | UNKNOWN | NCT05616715 |
| Peek device | Device | Approved | Gummy Smile | UNKNOWN | NCT05616715 |
| NexGen LPS-Flex Mobile Bearing Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00854295 |
| NexGen LPS-Flex Mobile Bearing Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00854295 |
| Vanguard CR Knee System | Other | Approved | Osteoarthritis | TERMINATED | NCT02175576 |
| Vanguard XP Bicruciate Knee System | Other | Approved | Osteoarthritis | TERMINATED | NCT02175576 |
| Microbial ID test | Other | Preclinical | Periprosthetic Joint Infection | UNKNOWN | NCT05320354 |
| Microbial ID test | Other | Preclinical | Periprosthetic Joint Infection | ENROLLING_BY_INVITATION | NCT05320354 |
| PBS | Other | Approved | Osteoarthritis Knee | COMPLETED | NCT01934218 |
| Gel-One | Other | Approved | Osteoarthritis Knee | COMPLETED | NCT01934218 |
| PBS | Other | Approved | Osteoarthritis Knee | COMPLETED | NCT01934218 |
| Gel-One | Other | Approved | Osteoarthritis Knee | COMPLETED | NCT01934218 |
| PBS | Other | Approved | Osteoarthritis Knee | COMPLETED | NCT01934218 |
| Gel-One | Other | Approved | Osteoarthritis Knee | COMPLETED | NCT01934218 |
| Persona Partial Knee System | Other | Approved | Degenerative Joint Disease of Knee | WITHDRAWN | NCT05037734 |
| Subchondroplasty Procedure | Procedure | Preclinical | Bone Marrow Lesions | COMPLETED | NCT03430219 |
| Subchondroplasty Procedure | Procedure | Preclinical | Bone Marrow Lesions | COMPLETED | NCT03430219 |
| ComPreSs Distal Femoral Replacement System. | Other | Phase PHASE1 | Lower Thighbone and Knee Joint Replacement | COMPLETED | NCT00591812 |
| ComPreSs Distal Femoral Replacement System. | Other | Phase PHASE1 | Lower Thighbone and Knee Joint Replacement | COMPLETED | NCT00591812 |
| ROSA assisted TKA | Other | Approved | Total Knee Arthoplasty | COMPLETED | NCT04982198 |
| ROSA assisted TKA | Other | Approved | Total Knee Arthoplasty | COMPLETED | NCT04982198 |
| High-Flexion Knee Replacement System using Cementless Fixation | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01194817 |
| High-Flexion Knee Replacement System using Cemented Fixation | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01194817 |
| High-Flexion Knee Replacement System using Cementless Fixation | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01194817 |
| High-Flexion Knee Replacement System using Cemented Fixation | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01194817 |
| SureLock All-Suture Anchor | Other | Preclinical | Shoulder Pain | TERMINATED | NCT04093700 |
| SureLock All-Suture Anchor | Other | Preclinical | Shoulder Pain | TERMINATED | NCT04093700 |
| Sirius stem | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| E1 (Exceed cup) | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Arcom (Exceed cup) | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Optipac | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Optivac | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Sirius stem | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| E1 (Exceed cup) | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Arcom (Exceed cup) | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Optipac | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Optivac | Other | Approved | Osteoarthritis | COMPLETED | NCT02307331 |
| Attune TKR | Other | Preclinical | Knee Osteoarthritis | TERMINATED | NCT03580772 |
| Persona TKR | Other | Preclinical | Knee Osteoarthritis | TERMINATED | NCT03580772 |
| Attune TKR | Other | Preclinical | Knee Osteoarthritis | TERMINATED | NCT03580772 |
| Persona TKR | Other | Preclinical | Knee Osteoarthritis | TERMINATED | NCT03580772 |
| Zimmer Persona Total Knee System | Other | Approved | Osteoarthritis | COMPLETED | NCT01859130 |
| Saline | Other | Approved | Osteoarthritis | COMPLETED | NCT02905240 |
| nSTRIDE APS | Other | Approved | Osteoarthritis | COMPLETED | NCT02905240 |
| Oxford Uni Knee | Other | Approved | Osteoarthritis, Knee | UNKNOWN | NCT00679120 |
| Oxford Uni Knee | Other | Approved | Osteoarthritis, Knee | UNKNOWN | NCT00679120 |
| Oxford Uni Knee | Other | Approved | Osteoarthritis, Knee | UNKNOWN | NCT00679120 |
| GTS cementless stem | Other | Approved | Osteoarthritis, Hip | ACTIVE_NOT_RECRUITING | NCT02851992 |
| GTS cementless stem | Other | Approved | Osteoarthritis, Hip | ACTIVE_NOT_RECRUITING | NCT02851992 |
| G7 Freedom Constrained Liners | Other | Preclinical | Hip Osteoarthritis | WITHDRAWN | NCT04093739 |
| G7 Freedom Constrained Liners | Other | Preclinical | Hip Osteoarthritis | WITHDRAWN | NCT04093739 |
| G7 Freedom Constrained Liners | Other | Preclinical | Hip Osteoarthritis | WITHDRAWN | NCT04093739 |
| RibFix Advantage | Other | Preclinical | Rib Fractures | TERMINATED | NCT05179005 |
| RibFix Advantage | Other | Preclinical | Rib Fractures | TERMINATED | NCT05179005 |
| HTR-PEKK | Other | Preclinical | Tumor | COMPLETED | NCT04931056 |
| Add-on Condyle | Other | Preclinical | Tumor | COMPLETED | NCT04931056 |
| Titanium Mandibular Plates | Other | Preclinical | Tumor | COMPLETED | NCT04931056 |
| Titanium Facial Plates | Other | Preclinical | Tumor | COMPLETED | NCT04931056 |
| Non surgical and Surgical | Other | Preclinical | Rib; Fracture | RECRUITING | NCT05146986 |
| Non surgical and Surgical | Other | Preclinical | Rib; Fracture | RECRUITING | NCT05146986 |
| Non surgical and Surgical | Other | Preclinical | Rib; Fracture | RECRUITING | NCT05146986 |
| Vanguard Rocc | Other | Preclinical | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03664791 |
| Vanguard Rocc | Other | Preclinical | Osteoarthritis, Knee | UNKNOWN | NCT03664791 |
| Palacos Bone Cement | Other | Approved | Hip Arthritis | COMPLETED | NCT01289834 |
| Hi-Fatigue Bone Cement | Other | Approved | Hip Arthritis | COMPLETED | NCT01289834 |
| Palacos Bone Cement | Other | Approved | Hip Arthritis | COMPLETED | NCT01289834 |
| Hi-Fatigue Bone Cement | Other | Approved | Hip Arthritis | COMPLETED | NCT01289834 |
| NexGen Total Knee | Other | Approved | Knee Pain | COMPLETED | NCT03969654 |
| Vanguard Total Knee | Other | Approved | Knee Pain | COMPLETED | NCT03969654 |
| PERSONA Total Knee | Other | Approved | Knee Pain | COMPLETED | NCT03969654 |
| NexGen Total Knee | Other | Approved | Knee Pain | COMPLETED | NCT03969654 |
| Vanguard Total Knee | Other | Approved | Knee Pain | COMPLETED | NCT03969654 |
| PERSONA Total Knee | Other | Approved | Knee Pain | COMPLETED | NCT03969654 |
| Cementless Vanguard DD RP | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT04076202 |
| Cementless Vanguard DD RP | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT04076202 |
| Biomet TMJ Replacement System | Other | Preclinical | Arthroplasty | COMPLETED | NCT00762944 |
| Biomet TMJ Replacement System | Other | Preclinical | Arthroplasty | COMPLETED | NCT00762944 |
| Biomet TMJ Replacement System | Other | Preclinical | Arthroplasty | COMPLETED | NCT00762944 |
| Arthroplasty hip | Other | Preclinical | Arthroplasty, Replacement, Hip | ACTIVE_NOT_RECRUITING | NCT02371382 |
| Primoris | Other | Preclinical | Coxarthrosis | ACTIVE_NOT_RECRUITING | NCT01326832 |
| Primoris | Other | Preclinical | Coxarthrosis | ACTIVE_NOT_RECRUITING | NCT01326832 |
| Zimmer Persona Knee-PS | Other | Approved | Osteoarthritis, Knee | ENROLLING_BY_INVITATION | NCT03681977 |
| Zimmer MP Persona | Other | Approved | Osteoarthritis, Knee | ENROLLING_BY_INVITATION | NCT03681977 |
| Zimmer Persona Knee-PS | Other | Approved | Osteoarthritis, Knee | ENROLLING_BY_INVITATION | NCT03681977 |
| Zimmer MP Persona | Other | Approved | Osteoarthritis, Knee | ENROLLING_BY_INVITATION | NCT03681977 |
| Persona TM Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03589300 |
| Persona TM Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03589300 |
| conventional total knee arthroplasty | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05685693 |
| Robotic-assisted total knee arthroplasty (raTKA) | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05685693 |
| conventional total knee arthroplasty | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05685693 |
| Robotic-assisted total knee arthroplasty (raTKA) | Other | Approved | Knee Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT05685693 |
| MPS-Flex Total Knee Joint Prostheses | Other | Preclinical | Total Knee Arthroplasty | SUSPENDED | NCT04427722 |
| MPS-Flex Total Knee Joint Prostheses | Other | Preclinical | Total Knee Arthroplasty | SUSPENDED | NCT04427722 |
| Total Hip Arthroplasty using MOTIVATION HIP Total Hip System | Other | Preclinical | Total Hip Arthroplasty | SUSPENDED | NCT03892005 |
| Total Hip Arthroplasty using MOTIVATION HIP Total Hip System | Other | Preclinical | Total Hip Arthroplasty | SUSPENDED | NCT03892005 |
| Dental Implant Placement | Other | Approved | Edentulous Alveolar Ridge | ACTIVE_NOT_RECRUITING | NCT05219305 |
| Dental Implant Placement | Other | Approved | Edentulous Alveolar Ridge | ACTIVE_NOT_RECRUITING | NCT05219305 |
| Control Group | Other | Approved | Osteoarthritis of Hip | ACTIVE_NOT_RECRUITING | NCT02263209 |
| Bioguard Group | Other | Approved | Osteoarthritis of Hip | ACTIVE_NOT_RECRUITING | NCT02263209 |
| Persona fixed bearing knee system (All patients will receive Persona fixed bearing knee system) | Other | Preclinical | Knee Osteoarthritis | COMPLETED | NCT04461626 |
| Persona fixed bearing knee system (All patients will receive Persona fixed bearing knee system) | Other | Preclinical | Knee Osteoarthritis | COMPLETED | NCT04461626 |
| Persona fixed bearing knee system (All patients will receive Persona fixed bearing knee system) | Other | Preclinical | Knee Osteoarthritis | COMPLETED | NCT04461626 |
| Subchondroplasty Procedure with AccuFill | Procedure | Preclinical | Subchondral Cysts | ACTIVE_NOT_RECRUITING | NCT03494660 |
| Treatment of insufficiency fractures | Drug | Preclinical | Insufficiency Fractures | COMPLETED | NCT03087396 |
| Vanguard™ Patient-Specific Femur | Other | Preclinical | Osteoarthritis | COMPLETED | NCT00698854 |
| Vanguard™ Complete Knee System | Other | Preclinical | Osteoarthritis | COMPLETED | NCT00698854 |
| Vanguard™ Patient-Specific Femur | Other | Preclinical | Osteoarthritis | COMPLETED | NCT00698854 |
| Vanguard™ Complete Knee System | Other | Preclinical | Osteoarthritis | COMPLETED | NCT00698854 |
| Metal on Metal | Other | Approved | Osteoarthritis | COMPLETED | NCT00754520 |
| Ceramic On Metal | Other | Approved | Osteoarthritis | COMPLETED | NCT00754520 |
| Metal on Metal | Other | Approved | Osteoarthritis | COMPLETED | NCT00754520 |
| Ceramic On Metal | Other | Approved | Osteoarthritis | COMPLETED | NCT00754520 |
| Metal on Metal | Other | Approved | Osteoarthritis | COMPLETED | NCT00754520 |
| Ceramic On Metal | Other | Approved | Osteoarthritis | COMPLETED | NCT00754520 |
| Fitmore Hip Stem | Other | Preclinical | Osteoarthritis | COMPLETED | NCT03411044 |
| Fitmore Hip Stem | Other | Preclinical | Osteoarthritis | COMPLETED | NCT03411044 |
| Fitmore Hip Stem | Other | Preclinical | Osteoarthritis | COMPLETED | NCT03411044 |
| Avantage Reload cup | Other | Approved | Primary Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03357445 |
| Avantage Reload cup | Other | Approved | Primary Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03357445 |
| Serum Metal ion levels determined to monitor changes in chromium and cobalt levels | Other | Approved | Avascular Necrosis of Hip | COMPLETED | NCT03681639 |
| Serum Metal ion levels determined to monitor changes in chromium and cobalt levels | Other | Approved | Avascular Necrosis of Hip | COMPLETED | NCT03681639 |
| Injection of cBMA aspirate into the index leg | Other | Phase PHASE1 | Peripheral Artery Disease | COMPLETED | NCT02863926 |
| Injection of cBMA aspirate into the index leg | Other | Phase PHASE1 | Peripheral Artery Disease | COMPLETED | NCT02863926 |
| Cemented Total Knee Arthroplasty | Other | Approved | Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery | ACTIVE_NOT_RECRUITING | NCT06720012 |
| Conventional instruments | Device | Approved | Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery | ACTIVE_NOT_RECRUITING | NCT06720012 |
| Patient specific instrumentation (PSI) | Device | Approved | Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery | ACTIVE_NOT_RECRUITING | NCT06720012 |
| Cemented Total Knee Arthroplasty | Other | Approved | Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery | ACTIVE_NOT_RECRUITING | NCT06720012 |
| Conventional instruments | Device | Approved | Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery | ACTIVE_NOT_RECRUITING | NCT06720012 |
| Patient specific instrumentation (PSI) | Device | Approved | Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery | ACTIVE_NOT_RECRUITING | NCT06720012 |
| G7 Acetabular System | Other | Preclinical | Hip Fractures | ACTIVE_NOT_RECRUITING | NCT04031209 |
| G7 Acetabular System | Other | Preclinical | Hip Fractures | ACTIVE_NOT_RECRUITING | NCT04031209 |
| Stanmore | Other | Approved | Osteoarthritis of the Hip | COMPLETED | NCT01501955 |
| Metaphyseal Hip Prosthesis | Other | Approved | Osteoarthritis of the Hip | COMPLETED | NCT01501955 |
| Stanmore | Other | Approved | Osteoarthritis of the Hip | COMPLETED | NCT01501955 |
| Metaphyseal Hip Prosthesis | Other | Approved | Osteoarthritis of the Hip | COMPLETED | NCT01501955 |
| TAPESTRY Biointegrative Implant | Other | Preclinical | Insertional Achilles Tendinopathy | TERMINATED | NCT05998785 |
| TAPESTRY Biointegrative Implant | Other | Preclinical | Insertional Achilles Tendinopathy | TERMINATED | NCT05998785 |
| Total Hip Arthroplasty with Longevity IT Offset Liners | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | TERMINATED | NCT05980234 |
| Total Hip Arthroplasty with Longevity IT Oblique Liners | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | TERMINATED | NCT05980234 |
| Total Hip Arthroplasty with Longevity IT Offset Liners | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | TERMINATED | NCT05980234 |
| Total Hip Arthroplasty with Longevity IT Oblique Liners | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | TERMINATED | NCT05980234 |
| NexGen TM Modular Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03272373 |
| NexGen TM Monoblock Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03272373 |
| NexGen TM Modular Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03272373 |
| NexGen TM Monoblock Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03272373 |
| NexGen TM Modular Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03272373 |
| NexGen TM Monoblock Tibia | Other | Approved | Osteoarthritis | COMPLETED | NCT03272373 |
| M/L Taper with Kinectiv Technology Stems and Necks | Other | Preclinical | Hip Disease | TERMINATED | NCT04027140 |
| M/L Taper with Kinectiv Technology Stems and Necks | Other | Preclinical | Hip Disease | TERMINATED | NCT04027140 |
| Vivacit-E Liner | Other | Approved | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03226808 |
| Vivacit-E Liner | Other | Approved | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03226808 |
| Metal-on-Metal Articulation | Other | Preclinical | Avascular Necrosis | COMPLETED | NCT03382652 |
| Metal-on-Metal Articulation | Other | Preclinical | Avascular Necrosis | COMPLETED | NCT03382652 |
| SternaLock XP | Other | Preclinical | Rigid Plate Fixation | WITHDRAWN | NCT05578651 |
| SternaLock XP | Other | Preclinical | Rigid Plate Fixation | WITHDRAWN | NCT05578651 |
| Nexgen total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Persona total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Nexgen total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Persona total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Arcos Revision Stem System | Other | Preclinical | Osteoarthritis | COMPLETED | NCT01820611 |
| Arcos Revision Stem System | Other | Preclinical | Osteoarthritis | COMPLETED | NCT01820611 |
| ToggleLoc 2.9 mm Soft Tissue System | Other | Preclinical | Epicondylitis of the Elbow | COMPLETED | NCT05519228 |
| Vanguard™ Cruciate Retaining Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00753090 |
| Vanguard™ Deep Dish Rotating Platform Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00753090 |
| Vanguard™ Cruciate Retaining Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00753090 |
| Vanguard™ Deep Dish Rotating Platform Knee | Other | Approved | Osteoarthritis | COMPLETED | NCT00753090 |
| One of the following hip implants may be used within this arm of the study: G7 Acetabular System, Taperloc Complete System, Avenir and Avenir Complete Systems, and Echo Bi-Metric System | Other | Approved | Osteoarthritis, Hip | TERMINATED | NCT05497206 |
| Surgery | Procedure | Preclinical | Hip Osteoarthritis | TERMINATED | NCT04326010 |
| Preoperative CT Scan | Other | Approved | Osteoarthritis Shoulder | NOT_YET_RECRUITING | NCT06032416 |
| Preoperative CT Scan | Other | Approved | Osteoarthritis Shoulder | NOT_YET_RECRUITING | NCT06032416 |
| FastFrame External Fixation System - Knee Spanning or Damage Control Kit | Other | Approved | Fracture | TERMINATED | NCT04730739 |
| FastFrame External Fixation System - Knee Spanning or Damage Control Kit | Other | Approved | Fracture | TERMINATED | NCT04730739 |
| FastFrame External Fixation System - Knee Spanning or Damage Control Kit | Other | Approved | Fracture | TERMINATED | NCT04730739 |
| Comprehensive Nano | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03423953 |
| Persona (Zimmer) posterior stabilised cemented Trabecular Metal™ (Tibia and Femur) prosthesis | Other | Approved | Total Knee Replacement | RECRUITING | NCT04677907 |
| Persona (Zimmer) posterior stabilised uncemented Trabecular Metal™ (Tibia and Femur) prosthesis | Other | Approved | Total Knee Replacement | RECRUITING | NCT04677907 |
| Device: Vanguard Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: NexGen Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: Persona Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Nexgen total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Persona total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Persona Partial Knee system | Other | Approved | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03034811 |
| Taperloc Complete Stem | Other | Preclinical | Hip Arthritis | RECRUITING | NCT04028687 |
| Taperloc Complete Stem | Other | Preclinical | Hip Arthritis | RECRUITING | NCT04028687 |
| Fast-Fix 360 Meniscal Repair System | Other | Approved | Meniscal Tears | COMPLETED | NCT06899659 |
| JuggerStitch™ Meniscal Repair Device | Device | Approved | Meniscal Tears | COMPLETED | NCT06899659 |
| Fast-Fix 360 Meniscal Repair System | Other | Approved | Meniscal Tears | COMPLETED | NCT06899659 |
| JuggerStitch™ Meniscal Repair Device | Device | Approved | Meniscal Tears | COMPLETED | NCT06899659 |
| E1-Hip Bearing | Other | Preclinical | Osteoarthritis | TERMINATED | NCT02087449 |
| E1-Hip Bearing | Other | Preclinical | Osteoarthritis | TERMINATED | NCT02087449 |
| E1-Hip Bearing | Other | Preclinical | Osteoarthritis | TERMINATED | NCT02087449 |
| ASHCOM Shoulder System | Other | Preclinical | Rotator Cuff Injuries | TERMINATED | NCT04258605 |
| ASHCOM Shoulder System | Other | Preclinical | Rotator Cuff Injuries | TERMINATED | NCT04258605 |
| Anaverse Shoulder System | Other | Preclinical | Rotator Cuff Injuries | TERMINATED | NCT05215600 |
| Anaverse Shoulder System | Other | Preclinical | Rotator Cuff Injuries | TERMINATED | NCT05215600 |
| ROSA PSA Subvastus Approach | Other | Phase PHASE4 | Knee Osteoarthritis | RECRUITING | NCT06267482 |
| ROSA PSA Parapatellar Approach | Other | Phase PHASE4 | Knee Osteoarthritis | RECRUITING | NCT06267482 |
| ROSA PSA Subvastus Approach | Other | Phase PHASE4 | Knee Osteoarthritis | RECRUITING | NCT06267482 |
| ROSA PSA Parapatellar Approach | Other | Phase PHASE4 | Knee Osteoarthritis | RECRUITING | NCT06267482 |
| No tourniquet | Other | Approved | Arthritis Knee | COMPLETED | NCT04923724 |
| tourniquet | Other | Approved | Arthritis Knee | COMPLETED | NCT04923724 |
| No tourniquet | Other | Approved | Arthritis Knee | COMPLETED | NCT04923724 |
| tourniquet | Other | Approved | Arthritis Knee | COMPLETED | NCT04923724 |
| No tourniquet | Other | Approved | Arthritis Knee | COMPLETED | NCT04923724 |
| tourniquet | Other | Approved | Arthritis Knee | COMPLETED | NCT04923724 |
| ArComXL® Polyethylene | Other | Preclinical | Osteoarthritis of Hip | COMPLETED | NCT00565786 |
| ArCom® Polyethylene | Other | Preclinical | Osteoarthritis of Hip | COMPLETED | NCT00565786 |
| ArComXL® Polyethylene | Other | Preclinical | Osteoarthritis of Hip | COMPLETED | NCT00565786 |
| ArCom® Polyethylene | Other | Preclinical | Osteoarthritis of Hip | COMPLETED | NCT00565786 |
| Fracture Shoulder Arthroplasty | Other | Approved | Fracture | COMPLETED | NCT02465398 |
| Fracture Shoulder Arthroplasty | Other | Approved | Fracture | COMPLETED | NCT02465398 |
| G7 Dual Mobility Longevity bearing | Other | Approved | Hip Osteoarthritis | ENROLLING_BY_INVITATION | NCT05548972 |
| G7 Dual Mobility with Vivacit-E bearing | Other | Approved | Hip Osteoarthritis | ENROLLING_BY_INVITATION | NCT05548972 |
| G7 Dual Mobility Longevity bearing | Other | Approved | Hip Osteoarthritis | ENROLLING_BY_INVITATION | NCT05548972 |
| G7 Dual Mobility with Vivacit-E bearing | Other | Approved | Hip Osteoarthritis | ENROLLING_BY_INVITATION | NCT05548972 |
| G7 Dual Mobility hip | Other | Preclinical | Clinical Outcomes | ACTIVE_NOT_RECRUITING | NCT03308929 |
| G7 Dual Mobility hip | Other | Preclinical | Clinical Outcomes | ACTIVE_NOT_RECRUITING | NCT03308929 |
| Vivacit-E and Longevity (HXLPE) Liners | Other | Approved | Total Hip Arthroplasty | RECRUITING | NCT04754087 |
| Vivacit-E and Longevity (HXLPE) Liners | Other | Approved | Total Hip Arthroplasty | RECRUITING | NCT04754087 |
| Avenir Complete Femoral Stem | Other | Approved | Osteoarthritis, Hip | ACTIVE_NOT_RECRUITING | NCT04731077 |
| Total hip arthoplasty (THA) | Other | Preclinical | Osteoarthritis, Hip | ACTIVE_NOT_RECRUITING | NCT04349046 |
| Total hip arthoplasty (THA) | Other | Preclinical | Osteoarthritis, Hip | ACTIVE_NOT_RECRUITING | NCT04349046 |
| Continuum Metal on Polyethylene Acetabular System | Other | Preclinical | Avascular Necrosis | ACTIVE_NOT_RECRUITING | NCT01307384 |
| Continuum Metal on Polyethylene Acetabular System | Other | Preclinical | Avascular Necrosis | ACTIVE_NOT_RECRUITING | NCT01307384 |
| Persona (Zimmer) posterior stabilised cemented Trabecular Metal™ (Tibia and Femur) prosthesis | Other | Approved | Total Knee Replacement | RECRUITING | NCT04677907 |
| Persona (Zimmer) posterior stabilised uncemented Trabecular Metal™ (Tibia and Femur) prosthesis | Other | Approved | Total Knee Replacement | RECRUITING | NCT04677907 |
| EZ Pass Suture Passer | Other | Preclinical | Anterior Cruciate Ligament Injury | COMPLETED | NCT03914703 |
| EZ Pass Suture Passer | Other | Preclinical | Anterior Cruciate Ligament Injury | COMPLETED | NCT03914703 |
| EZ Pass Suture Passer | Other | Preclinical | Anterior Cruciate Ligament Injury | COMPLETED | NCT03914703 |
| Comprehensive Primary Revision Stems | Other | Preclinical | Shoulder Pain | RECRUITING | NCT06788717 |
| Comprehensive Primary Revision Stems | Other | Preclinical | Shoulder Pain | RECRUITING | NCT06788717 |
| Oxford Cemented Partial Knee | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT01473134 |
| Oxford Cementless Partial Knee | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT01473134 |
| Oxford Cemented Partial Knee | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT01473134 |
| Oxford Cementless Partial Knee | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT01473134 |
| ActivBraid™Collagen Co-Braid suture (Zimmer Biomet) | Other | Preclinical | Rotator Cuff Repair of the Shoulder | RECRUITING | NCT06971497 |
| ActivBraid™Collagen Co-Braid suture (Zimmer Biomet) | Other | Preclinical | Rotator Cuff Repair of the Shoulder | RECRUITING | NCT06971497 |
| Fracture fixation via Intramedullary Nailing | Other | Preclinical | Osteotomy | ACTIVE_NOT_RECRUITING | NCT05362864 |
| Fracture fixation via Intramedullary Nailing | Other | Preclinical | Osteotomy | ACTIVE_NOT_RECRUITING | NCT05362864 |
| Reverse TESS V3 | Other | Preclinical | Osteoarthritis Shoulder | ACTIVE_NOT_RECRUITING | NCT05002959 |
| Anatomic TESS V3 | Other | Preclinical | Osteoarthritis Shoulder | ACTIVE_NOT_RECRUITING | NCT05002959 |
| Surgical stabilization | Other | Approved | Chronic Ankle Instability | COMPLETED | NCT02998333 |
| Total Hip Arthroplasty with G7 Freedom Constrained Vivacit-E Liners | Other | Approved | Osteoarthritis, Hip | ENROLLING_BY_INVITATION | NCT05587244 |
| Total Hip Arthroplasty with G7 Freedom Constrained Vivacit-E Liners | Other | Approved | Osteoarthritis, Hip | ENROLLING_BY_INVITATION | NCT05587244 |
| Synovasure® RISC™ Panel | Other | Preclinical | Arthritis, Inflammatory | COMPLETED | NCT05778162 |
| Persona Revision Knee System | Other | Preclinical | Arthroplasty Complications | RECRUITING | NCT04821154 |
| Persona Revision Knee System | Other | Preclinical | Arthroplasty Complications | RECRUITING | NCT04821154 |
| Zimmer Biomet Persona Ti-Nidium Total Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT04817969 |
| Zimmer Biomet Persona Ti-Nidium Total Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT04817969 |
| Zimmer Biomet Persona Ti-Nidium Total Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT04817969 |
| Synovasure® Comprehensive Infection Panel | Other | Preclinical | PJI | COMPLETED | NCT06153446 |
| Synovasure® Comprehensive Infection Panel | Other | Preclinical | PJI | COMPLETED | NCT06153446 |
| Synovasure® Comprehensive Infection Panel | Other | Preclinical | PJI | COMPLETED | NCT06153446 |
| Subchondroplasty Procedure with AccuFill | Procedure | Preclinical | Bone Marrow Edema | TERMINATED | NCT03110224 |
| Subchondroplasty Procedure with AccuFill | Procedure | Preclinical | Bone Marrow Edema | TERMINATED | NCT03110224 |
| Regenerex Tissue Attachment Augments | Other | Preclinical | Arthroplasty Complications | ACTIVE_NOT_RECRUITING | NCT06615739 |
| Identity Stem | Other | Approved | Shoulder Fractures | RECRUITING | NCT04984291 |
| Alliance Glenoid | Other | Approved | Shoulder Fractures | RECRUITING | NCT04984291 |
| Identity Stem | Other | Approved | Shoulder Fractures | RECRUITING | NCT04984291 |
| Alliance Glenoid | Other | Approved | Shoulder Fractures | RECRUITING | NCT04984291 |
| Identity Stem | Other | Approved | Shoulder Fractures | RECRUITING | NCT04984291 |
| Alliance Glenoid | Other | Approved | Shoulder Fractures | RECRUITING | NCT04984291 |
| Comprehensive Mini Humeral Tray | Other | Approved | Arthropathy of Shoulder Region | ACTIVE_NOT_RECRUITING | NCT03726554 |
| Comprehensive Reverse Porous Augmented Glenoid | Other | Approved | Arthropathy of Shoulder Region | ACTIVE_NOT_RECRUITING | NCT03726554 |
| Comprehensive Mini Humeral Tray | Other | Approved | Arthropathy of Shoulder Region | ACTIVE_NOT_RECRUITING | NCT03726554 |
| Comprehensive Reverse Porous Augmented Glenoid | Other | Approved | Arthropathy of Shoulder Region | ACTIVE_NOT_RECRUITING | NCT03726554 |
| Nexel Total Elbow | Other | Approved | Elbow Joint Destruction | RECRUITING | NCT02469662 |
| Nexel Total Elbow | Other | Approved | Elbow Joint Destruction | RECRUITING | NCT02469662 |
| Zimmer Trabecular Metal Total Ankle System | Other | Approved | Degenerative Arthritis | ACTIVE_NOT_RECRUITING | NCT02038140 |
| Trabecular Metal Reverse Shoulder System | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01480440 |
| Trabecular Metal Reverse Shoulder System | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01480440 |
| Comprehensive Anatomic Versa-Dial Titanium Humeral Head | Other | Preclinical | Shoulder Pain | ENROLLING_BY_INVITATION | NCT04003311 |
| Comprehensive Primary Micro Stem | Other | Preclinical | Shoulder Pain | ENROLLING_BY_INVITATION | NCT04003311 |
| Comprehensive Anatomic Versa-Dial Titanium Humeral Head | Other | Preclinical | Shoulder Pain | ENROLLING_BY_INVITATION | NCT04003311 |
| Comprehensive Primary Micro Stem | Other | Preclinical | Shoulder Pain | ENROLLING_BY_INVITATION | NCT04003311 |
| Biomet Cannulated Screw: 3.0, 4.0, 5.0, 6.5, and 8.0mm screws. | Other | Preclinical | Fractures, Bone | ACTIVE_NOT_RECRUITING | NCT04002518 |
| Biomet Cannulated Screw: 3.0, 4.0, 5.0, 6.5, and 8.0mm screws. | Other | Preclinical | Fractures, Bone | ACTIVE_NOT_RECRUITING | NCT04002518 |
| Biomet Cannulated Screw: 3.0, 4.0, 5.0, 6.5, and 8.0mm screws. | Other | Preclinical | Fractures, Bone | ACTIVE_NOT_RECRUITING | NCT04002518 |
| Biomet Comprehensive Shoulder System | Other | Preclinical | Osteoarthritis of the Shoulder | ACTIVE_NOT_RECRUITING | NCT03409718 |
| Biomet Comprehensive Shoulder System | Other | Preclinical | Osteoarthritis of the Shoulder | ACTIVE_NOT_RECRUITING | NCT03409718 |
| Biomet Comprehensive Reverse Shoulder | Other | Preclinical | Arthropathy of Shoulder Region | ENROLLING_BY_INVITATION | NCT03404778 |
| Z1 Femoral Hip System | Other | Preclinical | Hip Osteoarthritis | RECRUITING | NCT07104279 |
| Z1 Femoral Hip System | Other | Preclinical | Hip Osteoarthritis | RECRUITING | NCT07104279 |
| humeral fracture | Other | Preclinical | Humeral Fractures, Proximal | RECRUITING | NCT05019664 |
| JuggerStitch Meniscal Repair Device | Device | Approved | Meniscus Tear, Tibial | RECRUITING | NCT04228367 |
| Tapestry Biointegrative Implant | Other | Preclinical | Rotator Cuff Tears | SUSPENDED | NCT06287853 |
| Tapestry Biointegrative Implant | Other | Preclinical | Rotator Cuff Tears | SUSPENDED | NCT06287853 |
| Tapestry Biointegrative Implant | Other | Preclinical | Rotator Cuff Tears | SUSPENDED | NCT06287853 |
| Revision arthroplasty | Other | Preclinical | Revision Arthroplasty | WITHDRAWN | NCT06699160 |
| Revision arthroplasty | Other | Preclinical | Revision Arthroplasty | WITHDRAWN | NCT06699160 |
| Femoral fixation with intramedullary nails | Other | Preclinical | Femur Fracture | RECRUITING | NCT05339360 |
| Femoral fixation with intramedullary nails | Other | Preclinical | Femur Fracture | RECRUITING | NCT05339360 |
| ZNN Bactiguard tibia | Other | Preclinical | Tibial Fractures | RECRUITING | NCT05022485 |
| ZNN Bactiguard tibia | Other | Preclinical | Tibial Fractures | RECRUITING | NCT05022485 |
| Hip Arthroplasty | Other | Approved | Osteoarthrosis | ACTIVE_NOT_RECRUITING | NCT02518269 |
| Hip Arthroplasty | Other | Approved | Osteoarthrosis | ACTIVE_NOT_RECRUITING | NCT02518269 |
| Shoulder Arthroplasty | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | ACTIVE_NOT_RECRUITING | NCT01700543 |
| Shoulder Arthroplasty | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | ACTIVE_NOT_RECRUITING | NCT01700543 |
| Shoulder Arthroplasty | Other | Preclinical | Non-inflammatory Degenerative Joint Disease (NIDJD) | ACTIVE_NOT_RECRUITING | NCT01700543 |
| Vanguard 360 TiNbN Femur with PSC bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard 360 TiNbN Femur with PS bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard DA 360 | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard SSK 360 with PSC bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard SSK 360 with PS Bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard 360 TiNbN Femur with PSC bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard 360 TiNbN Femur with PS bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard DA 360 | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard SSK 360 with PSC bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| Vanguard SSK 360 with PS Bearing | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT01542580 |
| AGC knee | Other | Approved | Osteoarthritis | COMPLETED | NCT01064063 |
| Vanguard CR | Other | Approved | Osteoarthritis | COMPLETED | NCT01064063 |
| AGC knee | Other | Approved | Osteoarthritis | COMPLETED | NCT01064063 |
| Vanguard CR | Other | Approved | Osteoarthritis | COMPLETED | NCT01064063 |
| AGC knee | Other | Approved | Osteoarthritis | COMPLETED | NCT01064063 |
| Vanguard CR | Other | Approved | Osteoarthritis | COMPLETED | NCT01064063 |
| JuggerLoc soft tissue device | Device | Preclinical | Bankart Lesions | COMPLETED | NCT05584553 |
| ToggleLoc 2.9 mm soft tissue device | Device | Preclinical | Bankart Lesions | COMPLETED | NCT05584553 |
| JuggerLoc soft tissue device | Device | Preclinical | Bankart Lesions | COMPLETED | NCT05584553 |
| ToggleLoc 2.9 mm soft tissue device | Device | Preclinical | Bankart Lesions | COMPLETED | NCT05584553 |
| Total Hip arthroplasty | Other | Preclinical | Total Hip and Knee Arthroplasties | RECRUITING | NCT06699134 |
| Total knee arthroplasty | Other | Preclinical | Total Hip and Knee Arthroplasties | RECRUITING | NCT06699134 |
| Total Hip arthroplasty | Other | Preclinical | Total Hip and Knee Arthroplasties | RECRUITING | NCT06699134 |
| Total knee arthroplasty | Other | Preclinical | Total Hip and Knee Arthroplasties | RECRUITING | NCT06699134 |
| Alliance™ Glenoid | Other | Preclinical | Shoulder Fractures | RECRUITING | NCT06920459 |
| Alliance™ Glenoid | Other | Preclinical | Shoulder Fractures | RECRUITING | NCT06920459 |
| Alliance™ Glenoid | Other | Preclinical | Shoulder Fractures | RECRUITING | NCT06920459 |
| Cemented Persona Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT05630053 |
| Cementless Persona Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT05630053 |
| Zimmer Biomet Persona total knee system | Other | Preclinical | Knee Arthropathy | ACTIVE_NOT_RECRUITING | NCT03495232 |
| Zimmer Biomet Persona total knee system | Other | Preclinical | Knee Arthropathy | ACTIVE_NOT_RECRUITING | NCT03495232 |
| Ceramic on Ceramic articulation | Other | Preclinical | Noninflammatory Degenerative Joint Disease | COMPLETED | NCT02036931 |
| Ceramic on Polyethylene articulation | Other | Preclinical | Noninflammatory Degenerative Joint Disease | COMPLETED | NCT02036931 |
| Metal on Polyethylene articulation | Other | Preclinical | Noninflammatory Degenerative Joint Disease | COMPLETED | NCT02036931 |
| Ceramic on Ceramic articulation | Other | Preclinical | Noninflammatory Degenerative Joint Disease | COMPLETED | NCT02036931 |
| Ceramic on Polyethylene articulation | Other | Preclinical | Noninflammatory Degenerative Joint Disease | COMPLETED | NCT02036931 |
| Metal on Polyethylene articulation | Other | Preclinical | Noninflammatory Degenerative Joint Disease | COMPLETED | NCT02036931 |
| Comprehensive SRS Replacement | Other | Preclinical | Degenerative Disease | ACTIVE_NOT_RECRUITING | NCT03270982 |
| Comprehensive SRS Replacement | Other | Preclinical | Degenerative Disease | ACTIVE_NOT_RECRUITING | NCT03270982 |
| Conventional cohort | Other | Phase PHASE4 | Serum Metal Levels, Specifically Cobalt, Chromium, and Titanium | ACTIVE_NOT_RECRUITING | NCT03371212 |
| Dual mobility cohort | Other | Phase PHASE4 | Serum Metal Levels, Specifically Cobalt, Chromium, and Titanium | ACTIVE_NOT_RECRUITING | NCT03371212 |
| Conventional cohort | Other | Phase PHASE4 | Serum Metal Levels, Specifically Cobalt, Chromium, and Titanium | ACTIVE_NOT_RECRUITING | NCT03371212 |
| Dual mobility cohort | Other | Phase PHASE4 | Serum Metal Levels, Specifically Cobalt, Chromium, and Titanium | ACTIVE_NOT_RECRUITING | NCT03371212 |
| Total Knee Arthroplasty | Other | Preclinical | Knee Pain Chronic | RECRUITING | NCT05787821 |
| Total Knee Arthroplasty | Other | Preclinical | Knee Pain Chronic | RECRUITING | NCT05787821 |
| Device: Vanguard Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: NexGen Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: Persona Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: Vanguard Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: NexGen Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: Persona Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| ZNN Bactiguard Retrograde Femoral Nail | Other | Preclinical | Femoral Fracture | RECRUITING | NCT05276674 |
| ZNN Bactiguard Retrograde Femoral Nail | Other | Preclinical | Femoral Fracture | RECRUITING | NCT05276674 |
| ExploR Radial Head | Other | Preclinical | Elbow Injury | ENROLLING_BY_INVITATION | NCT05583448 |
| ExploR Radial Head | Other | Preclinical | Elbow Injury | ENROLLING_BY_INVITATION | NCT05583448 |
| Comprehensive Reverse Versa-Dial Titanium Glenosphere | Other | Preclinical | Shoulder Pain | ENROLLING_BY_INVITATION | NCT04003272 |
| Tapestry Biointegrative Implant | Other | Preclinical | Tendon Injuries- Subscapularis | ENROLLING_BY_INVITATION | NCT05735119 |
| Tapestry Biointegrative Implant | Other | Preclinical | Tendon Injuries- Subscapularis | ENROLLING_BY_INVITATION | NCT05735119 |
| Clavicle open reduction and internal fixation | Other | Approved | Clavicle Fracture | ACTIVE_NOT_RECRUITING | NCT05327959 |
| A.L.P.S. Proximal Humerus Plating System | Other | Approved | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03626038 |
| A.L.P.S. Proximal Humerus Plating System | Other | Approved | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03626038 |
| OsseoFit Stemless Onlay | Other | Preclinical | Shoulder Injuries | NOT_YET_RECRUITING | NCT07421245 |
| OsseoFit Stemless Inlay | Other | Preclinical | Shoulder Injuries | NOT_YET_RECRUITING | NCT07421245 |
| Avitus Bone Harvester | Other | Approved | Bone Graft | RECRUITING | NCT07434505 |
| Total knee arthroplasty | Other | Preclinical | Rhematoid Arthritis | NOT_YET_RECRUITING | NCT07286513 |
| Total Knee Arthroplasty | Other | Approved | Knee Arthroplasty, Total | COMPLETED | NCT07009912 |
| Total Knee Arthroplasty | Other | Approved | Knee Arthroplasty, Total | COMPLETED | NCT07009912 |
| Persona IQ | Other | Preclinical | Osteo Arthritis Knee | ENROLLING_BY_INVITATION | NCT06089291 |
| Persona IQ | Other | Preclinical | Osteo Arthritis Knee | ENROLLING_BY_INVITATION | NCT06089291 |
| Zimmer Persona Total Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT02255383 |
| Zimmer Persona Total Knee System | Other | Approved | Knee Pain Chronic | ACTIVE_NOT_RECRUITING | NCT02255383 |
| Endo II Femoral Head | Other | Preclinical | Hip Arthritis | ENROLLING_BY_INVITATION | NCT05199870 |
| RingLoc Bipolar Acetabular Cup | Other | Preclinical | Hip Arthritis | ENROLLING_BY_INVITATION | NCT05199870 |
| Endo II Femoral Head | Other | Preclinical | Hip Arthritis | ENROLLING_BY_INVITATION | NCT05199870 |
| RingLoc Bipolar Acetabular Cup | Other | Preclinical | Hip Arthritis | ENROLLING_BY_INVITATION | NCT05199870 |
| mymobility with Apple Watch | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03737149 |
| mymobility with Apple Watch | Other | Approved | Osteoarthritis, Knee | COMPLETED | NCT03737149 |
| The RibFix Titan™ device should be used within this arm of the study. | Device | Preclinical | Rib Fracture | RECRUITING | NCT07485829 |
| AS Domelock System | Other | Preclinical | Avascular Necrosis | ACTIVE_NOT_RECRUITING | NCT03312465 |
| Vivacit-E Elevated Liners | Other | Preclinical | Osteoarthritis (OA) of the Hip | ENROLLING_BY_INVITATION | NCT07150221 |
| Vivacit-E Elevated Liners | Other | Preclinical | Osteoarthritis (OA) of the Hip | ENROLLING_BY_INVITATION | NCT07150221 |
| Vivacit-E Elevated Liners | Other | Preclinical | Osteoarthritis (OA) of the Hip | ENROLLING_BY_INVITATION | NCT07150221 |
| Total Knee Replacement (TKR) | Other | Preclinical | Osteo Arthritis Knee | RECRUITING | NCT05966519 |
| Total Knee Replacement (TKR) | Other | Preclinical | Osteo Arthritis Knee | RECRUITING | NCT05966519 |
| Total Knee Replacement (TKR) | Other | Preclinical | Osteo Arthritis Knee | RECRUITING | NCT05966519 |
| Treatment of insufficiency fractures | Drug | Preclinical | Insufficiency Fractures | COMPLETED | NCT03087396 |
| The RibFix Titan™ device should be used within this arm of the study. | Device | Preclinical | Rib Fracture | RECRUITING | NCT07485829 |
| Total knee arthroplasty | Other | Preclinical | Rhematoid Arthritis | ENROLLING_BY_INVITATION | NCT07286513 |
| Total knee arthroplasty | Other | Preclinical | Rhematoid Arthritis | ENROLLING_BY_INVITATION | NCT07286513 |
| Subchondroplasty Procedure with AccuFill | Procedure | Preclinical | Subchondral Cysts | COMPLETED | NCT03494660 |
| Subchondroplasty Procedure with AccuFill | Procedure | Preclinical | Subchondral Cysts | COMPLETED | NCT03494660 |
| Comprehensive Nano | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03423953 |
| Comprehensive Nano | Other | Preclinical | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03423953 |
| Persona Partial Knee system | Other | Approved | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03034811 |
| Persona Partial Knee system | Other | Approved | Osteoarthritis | ACTIVE_NOT_RECRUITING | NCT03034811 |
| OsseoFit Stemless Onlay | Other | Preclinical | Shoulder Injuries | NOT_YET_RECRUITING | NCT07421245 |
| OsseoFit Stemless Inlay | Other | Preclinical | Shoulder Injuries | NOT_YET_RECRUITING | NCT07421245 |
| Nexgen total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Persona total knee system | Other | Approved | Osteoarthritis, Knee | ACTIVE_NOT_RECRUITING | NCT03073941 |
| Device: Vanguard Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: NexGen Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
| Device: Persona Total Knee | Device | Approved | Knee Pain | COMPLETED | NCT04338893 |
Total products: 996