| Recruiting | EMPHASYS Cup Positioning in THA With Non-Invasive Navigation (Velys Hip Navigation (VHN)) NCT06631638 | DePuy Orthopaedics | N/A |
| Recruiting | Post Market Clinical Follow-Up KeriFlex® NCT06546345 | Keri Medical SA | — |
| Active Not Recruiting | Perform® Humeral System - Fracture Study (PFX) NCT05773352 | Stryker Trauma and Extremities | — |
| Terminated | MDR - Longevity IT Oblique and Offset Liners NCT05980234 | Zimmer Biomet | — |
| Active Not Recruiting | Cemented vs Cementless Persona Keel RCT NCT05630053 | Zimmer Biomet | N/A |
| Recruiting | Persona OsseoTi Keel Compatibility Study (Total Knee Arthroplasty) NCT05787821 | Zimmer Biomet | — |
| Withdrawn | A Randomized Controlled Trial for Partial Knee Arthroplasty NCT05037734 | Zimmer Biomet | N/A |
| Enrolling By Invitation | Tornier HRS (Humeral Reconstruction System) Study (REVIVE) NCT05500066 | Stryker Trauma and Extremities | — |
| Recruiting | Hydrogel Coating to Reduce Post-surgical Infection After Joint Arthroplasty NCT05679232 | Medacta International SA | N/A |
| Active Not Recruiting | Pyrocarbon Clinical Follow-up Study NCT05049993 | Stryker Trauma and Extremities | — |
| Active Not Recruiting | The Medacta Quadra-P Anteverted Study NCT05460715 | Medacta International SA | — |
| Not Yet Recruiting | Prospective Post-market Study Examining the Effectiveness of the EcoFit® NCT04918680 | Implantcast North America, LLC | — |
| Active Not Recruiting | Persona Ti-Nidium Post-Market Clinical Follow-up NCT04817969 | Zimmer Biomet | N/A |
| Active Not Recruiting | The Medacta International GMK Sphere Cementless Post-Marketing Surveillance Study NCT05003414 | Medacta International SA | — |
| Active Not Recruiting | The Medacta International AMIStem-P Post-Marketing Surveillance Study NCT04997005 | Medacta International SA | — |
| Active Not Recruiting | Prospective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -Launay NCT06012656 | Medacta International SA | — |
| Completed | Persona TM Tibia Clinical Outcomes Study NCT03589300 | Zimmer Biomet | N/A |
| Completed | NexGen TM Tibia Clinical Outcomes Study NCT03272373 | Zimmer Biomet | N/A |
| Terminated | Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement NCT03247023 | Smith & Nephew, Inc. | — |
| Terminated | Clinical Evaluation of the Integra® Titan™ Modular Shoulder System Generation 2.5 for Primary Shoulder Joint R NCT03250767 | Smith & Nephew, Inc. | — |
| Recruiting | Physica System Total Knee Replacement Registry Study NCT03048201 | Limacorporate S.p.a | N/A |
| Active Not Recruiting | Persona Partial Knee Clinical Outcomes Study NCT03034811 | Zimmer Biomet | N/A |
| Terminated | Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting NCT02820766 | Smith & Nephew, Inc. | — |
| Completed | Actis Total Hip System 2 Year Follow-up NCT02783274 | DePuy Orthopaedics | N/A |
| Completed | Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty NCT02525783 | Stryker Trauma and Extremities | — |
| Recruiting | The Medacta International SMS Post-Marketing Surveillance Study NCT02748408 | Medacta International SA | — |
| Terminated | Randomized Controlled Clinical Outcomes of the Vanguard XP Bicruciate Knee System NCT02175576 | Zimmer Biomet | N/A |
| Active Not Recruiting | Persona Total Knee Arthroplasty Outcomes Study NCT02255383 | Zimmer Biomet | N/A |
| Completed | Efficacy of Intra-articular Collagen Injection in Patients With Knee Joint Pain Compared to Normal Saline Inje NCT02539095 | Cellontech Co., Ltd. | Phase 4 |
| Active Not Recruiting | Zimmer POLAR Persona - TKA (EMEA Study) NCT02337244 | Zimmer, GmbH | — |
| Completed | Zimmer POLAR - Total Knee Arthroplasty (TKA) NCT01859130 | Zimmer Biomet | N/A |
| Completed | Taperloc Complete Microplasty vs Taperloc Complete Standard: Randomized Controlled Study on Bone Mineral Densi NCT02087436 | Zimmer Biomet | N/A |
| Terminated | Evaluate E1 Wear, Clinical Performance of E1 Liner in THA in Korean Patient Population NCT02087449 | Zimmer Biomet | — |
| Unknown | Comparison of Efficacy and Safety of Microfracture and Modified Microfracture NCT02539030 | Cellontech Co., Ltd. | Phase 4 |
| Completed | The Post-marketing Surveillance to Evaluate the Efficacy of CHONDRON (Autologous Cultured Chondrocyte) by Arth NCT02539069 | Cellontech Co., Ltd. | N/A |
| Completed | The Post-marketing Surveillance to Evaluate the Efficacy and Safety of a CHONDRON (Autologous Cultured Chondro NCT02539056 | Cellontech Co., Ltd. | N/A |
| Active Not Recruiting | The Medacta International GMK Sphere Post-Marketing Surveillance Study NCT02199600 | Medacta International SA | N/A |
| Completed | A Prospective Munti-center Study on VANGUARD™ PS Total Knee Replacement System NCT01906177 | Zimmer Biomet | — |
| Completed | A Clinical Evaluation of Metal Ion Release From Metal-on-Metal Cementless Total Hip Arthroplasty NCT00757354 | Zimmer Biomet | N/A |
| Terminated | Post Market Study of the 3DKnee™ With E-plus Insert NCT01551472 | Encore Medical, L.P. | — |
| Active Not Recruiting | A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee NCT01542580 | Zimmer Biomet | — |
| Completed | Randomized Controlled Clinical Evaluation to Compare Vanguard Cruciate Retaining and AGC Total Condylar Knee I NCT01064063 | Zimmer Biomet | N/A |
| Unknown | Vanguard Rocc Post Market Surveillance NCT03664791 | Zimmer Biomet | — |
| Completed | Vanguard Complete Knee Versus Vanguard High Flex Rotating Platform (RP) Knee Study NCT01010269 | Zimmer Biomet | N/A |
| Completed | Prospective Multicenter Post Approval Study of the LPS-Flex Mobile Bearing Knee NCT00854295 | Zimmer Biomet | N/A |
| Terminated | Trilogy AB Acetabular Hip System Post Approval Study NCT00715026 | Zimmer Biomet | Phase 4 |
| Completed | Post-Market Study of the 3DKnee™ System NCT00819481 | Encore Medical, L.P. | — |
| Withdrawn | LPS Flex Porous Femoral Components NCT01462240 | Zimmer Biomet | — |
| Terminated | 3DKnee™ System vs. the MJS Knee System NCT00764803 | Encore Medical, L.P. | — |
| Withdrawn | A Clinical Investigation of Recovery Following Hip Resurfacing or Total Hip Arthroplasty NCT00585988 | Biomet Orthopedics, LLC | N/A |
| Withdrawn | Total Knee Replacement Using Simplex® or Cobalt™ Bone Cement NCT00589485 | Zimmer Biomet | — |
| Completed | A Clinical Investigation of the C2a-Taper™ Acetabular System NCT00578851 | Biomet Orthopedics, LLC | — |
| Terminated | Maxim® Knee Pop-Top® Tibia vs. Regular Maxim® Knee Tibia NCT00579059 | Biomet Orthopedics, LLC | N/A |
| Completed | A Clinical Investigation of the Vanguard™ Complete Knee System NCT00698854 | Zimmer Biomet | — |