| Recruiting | A Prospective, Post-Market, Clinical Follow-up Study of the Incompass™ Total Ankle System NCT07118501 | Stryker Trauma and Extremities | — |
| Not Yet Recruiting | A Multi-Center Study Assessing the Safety and Efficacy of the LEGION Medial Stabilized (MS) Insert in Patients NCT07199738 | Smith & Nephew, Inc. | — |
| Active Not Recruiting | A Multi-Centre Study in Patients Undergoing Total Hip Arthroplasty With the Smith+Nephew CATALYSTEM™ Primary H NCT06564636 | Smith & Nephew, Inc. | — |
| Active Not Recruiting | A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew's Porous Knee System in NCT05197036 | Smith & Nephew, Inc. | — |
| Recruiting | The KinematX Midcarpal Total Wrist Arthroplasty Registry NCT05719935 | Extremity Medical | — |
| Terminated | Anterior Advantage With KINCISE NCT04191733 | DePuy Orthopaedics | N/A |
| Active Not Recruiting | Post-Market Study of Comprehensive Reverse Augmented Glenoid and Mini Humeral Tray in Total Shoulder Arthropla NCT03726554 | Zimmer Biomet | N/A |
| Active Not Recruiting | Post Market Clinical Follow-up (PMCF) Study of the A.L.P.S. Proximal Humerus Plating System NCT03626038 | Zimmer Biomet | N/A |
| Completed | China ATTUNE® Study NCT03542045 | DePuy Orthopaedics | — |
| Terminated | GLOBAL ICON Stemless Shoulder System Post Market Clinical Follow Up Study NCT03168672 | DePuy Orthopaedics | N/A |
| Suspended | Clinical Evaluation of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement (CADENCE) NCT03142958 | Smith & Nephew, Inc. | — |
| Completed | ATTUNE Single-Use Instrumentation vs. ATTUNE Reusable Instrumentation in Primary Total Knee Arthroplasty NCT02574312 | DePuy Orthopaedics | N/A |
| Recruiting | Clinical Outcomes Study of the Nexel Total Elbow NCT02469662 | Zimmer Biomet | N/A |
| Completed | Project JAY THA Registration Study NCT02347384 | Smith & Nephew Orthopaedics (Beijing) Limited | N/A |
| Completed | TC-A Registration Study NCT02139345 | Smith & Nephew Medical (Shanghai) Ltd | N/A |
| Active Not Recruiting | Zimmer Trabecular Metal Total Ankle PMCF NCT02038140 | Zimmer Biomet | N/A |
| Completed | Robotic Arm Assisted Total Knee Arthroplasty NCT02058069 | MAKO Surgical Corp. | N/A |
| Terminated | Multi-centre Study to Assess the Long-term Performance of the Deltamotion Cup System in Primary Hip Replacemen NCT01635166 | DePuy International | Phase 4 |
| Terminated | 28mm Ceramic-on-Ceramic Total Hip Replacement Study NCT01657435 | DePuy Orthopaedics | — |
| Terminated | CoMplete™ Acetabular Hip System NCT01543230 | DePuy Orthopaedics | N/A |
| Withdrawn | Gender Solutions Natural Knee Post-Market Study NCT01463566 | Zimmer Biomet | — |
| Active Not Recruiting | AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study NCT03357445 | Zimmer Biomet | N/A |
| Active Not Recruiting | Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF) Study NCT01307384 | Zimmer Biomet | — |
| Terminated | Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder Arthroplasty NCT01480453 | Zimmer Biomet | — |
| Active Not Recruiting | Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder System NCT01480440 | Zimmer Biomet | — |
| Active Not Recruiting | Continuum Ceramic on Ceramic Bearing Post Market Clinical Follow-Up Study NCT03343171 | Zimmer Biomet | — |
| Terminated | An Electronic Data Capture Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Tota NCT01134445 | DePuy International | Phase 4 |
| Completed | 2-Year Post-Approval Study to Investigate the Scandinavian Total Ankle Replacement System (STAR) Ankle Under A NCT01284283 | Encore Medical, L.P. | N/A |
| Completed | Postmarketing Study to Determine Performance of the SIGMA HP® PARTIAL KNEE SYSTEM NCT01529099 | DePuy International | Phase 4 |
| Terminated | Minimally Invasive Versus Conventional Approaches in Navigated Total Knee Arthroplasty (TKA) NCT00839020 | Aesculap AG | Phase 4 |
| Completed | Ankle Joint Replacement Outcomes Study NCT00503438 | Smith & Nephew, Inc. | — |
| Terminated | Foundation Knee Study - Retrospective NCT00764894 | Encore Medical, L.P. | — |
| Terminated | A Single Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-ceramic Beari NCT00872222 | DePuy International | Phase 4 |
| Completed | The 3DKnee™ System: A Post-Market Study NCT00764673 | Encore Medical, L.P. | Phase 4 |
| Terminated | Postoperative Function Following Partial and Total Knee Replacement NCT00492219 | New Lexington Clinic | N/A |
| Terminated | Multi-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and Primary Tot NCT00872547 | DePuy International | Phase 4 |
| Completed | Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System NCT00487565 | DePuy Orthopaedics | N/A |
| Terminated | A Randomised Study to Compare Metal Ion Release and Long-term Performance of the Pinnacle™ Cup With a Ceramic- NCT00873444 | DePuy International | Phase 4 |
| Terminated | A Two Centre Study to Assess the Stability and Long-term Performance of the C-Stem™ AMT in a Total Primary Hip NCT00872573 | DePuy International | Phase 4 |
| Completed | A Study to Assess the Long-term Performance of SmartSet® HV and SmartSet® GHV Bone Cements in Primary Total Hi NCT00872066 | DePuy International | Phase 4 |
| Terminated | Post-approval Study of the DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System NCT00546598 | DePuy Orthopaedics | Phase 4 |
| Terminated | A Multi-centre Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip Replac NCT00208455 | DePuy International | Phase 4 |
| Withdrawn | A Multi-centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Polyethylene-on-metal Bea NCT00208429 | DePuy International | Phase 4 |
| Terminated | A Two Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Metal-on-Metal Bearing in P NCT00208364 | DePuy International | Phase 4 |
| Terminated | A Single Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing NCT00872794 | DePuy International | Phase 4 |
| Completed | Cementless Alumina-Alumina Total Hip and Hybrid NCT00764530 | Encore Medical, L.P. | N/A |
| Terminated | A Multi-centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing S NCT00208377 | DePuy International | Phase 4 |
| Terminated | A Multi-centre Study to Assess the Long-term Performance of the Summit™ Hip in Primary Total Hip Replacement NCT00208390 | DePuy International | Phase 4 |
| Terminated | Clinical Study Comparing Two Implant Surface Finishes in Patients Undergoing Cementless Total Hip Replacement NCT00306917 | DePuy Orthopaedics | N/A |
| Terminated | A Randomised Single Centre Study to Compare the Long-term Performance of Acryloc™ and Palacos® R Bone Cements NCT00208403 | DePuy International | Phase 4 |
| Terminated | Ascension® Post- Approval Study; PyroCarbon Metacarpophalangeal Total Joint Prosthesis NCT02408471 | Smith & Nephew, Inc. | N/A |
| Completed | Study of the Scandinavian Total Ankle Replacement (STAR) for the Treatment of Bilateral Degenerative Ankle Dis NCT00586781 | Link America, Inc. | Phase 3 |
| Completed | A Randomised Single Centre Study to Compare the Long-term Wear Characteristics of Marathon™ and Enduron™ Polye NCT00208442 | DePuy International | Phase 4 |
| Completed | Randomized Fixed Bearing vs Mobile Bearing Cruciate Substituting TKA NCT00289107 | DePuy Orthopaedics | N/A |
| Completed | Randomized Fixed Bearing vs Mobile Bearing Cruciate Retaining TKA NCT00289094 | DePuy Orthopaedics | N/A |
| Terminated | Primary TKA Cruciate Retaining vs Cruciate Substituting With Rotating Platform Knee Prostheses NCT00289081 | DePuy Orthopaedics | N/A |
| Terminated | A Randomised Multi-centre Study to Compare the Long-term Performance of the Future Hip to 3 Other Implants in NCT00208468 | DePuy International | Phase 3 |
| Completed | Mobile - Bearing Knee Study NCT00765362 | Encore Medical, L.P. | Phase 3 |
| Terminated | A Randomised Single Centre Study to Compare the Long-term Performance of 4 Designs of the DePuy Ultima LX Stem NCT00208351 | DePuy International | Phase 3 |