A Study of Participants Undergoing Radial Head Replacement Using the DePuy Synthes Radial Head Replacement System for Partial Replacement of the Elbow Joint
NCT05415592 · Status: WITHDRAWN · Type: OBSERVATIONAL
Last updated 2023-02-16
Summary
The purpose of this study is to establish survivorship defined by the cumulative incidence of revision over the first 6 months post-implantation.
Conditions
- Radial Head Fractures
Interventions
- DEVICE
-
DePuy Synthes Radial Head Replacement System
DePuy Synthes Radial Head Replacement System will be used for radial head replacement or partial replacement of the elbow joint.
Sponsors & Collaborators
-
DePuy Synthes Products, Inc.
lead INDUSTRY
Principal Investigators
-
DePuy Synthes Products, Inc. Clinical Trial · DePuy Synthes Products, Inc.
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-03-31
- Primary Completion
- 2026-03-31
- Completion
- 2030-03-31
- FDA Device
- Yes
Countries
- United States
- United Kingdom
Study Locations
More Related Trials
-
The Press Fit Condylar (P.F.C.) Sigma Rotating Platform (RP) TC3 Revision Knee in Revision Knee Arthroplasty
NCT00733681 ·Status: TERMINATED ·Phase: PHASE4
-
Study on Autologous Osteoblastic Cells Implantation to Early Stage Osteonecrosis of the Femoral Head
NCT01529008 ·Status: TERMINATED ·Phase: PHASE3
-
Continuation of Patient Follow-up to 2 Years for the Pinnacle RSA and Pinnacle DM RSA Clinical Trials
NCT05930067 ·Status: COMPLETED ·Phase: NA
-
MDR ExploR Radial Head System PMCF
NCT05583448 ·Status: ENROLLING_BY_INVITATION
-
Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement
NCT03247023 ·Status: TERMINATED
-
A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) System
NCT04089371 ·Status: TERMINATED
-
Roadmap for Succeeding in Bundled Payment for Orthopedic Joint Replacements
NCT02734043 ·Status: WITHDRAWN
-
LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study
NCT00510458 ·Status: COMPLETED ·Phase: NA
-
Assessment of HydroxyColl Bone Graft Substitute in High Tibial Osteotomy Wedge Grafting.
NCT03601130 ·Status: UNKNOWN ·Phase: NA
-
Long Term Sidus PMCF
NCT04063943 ·Status: WITHDRAWN ·Phase: NA
-
Thumb Hemi-Arthroplasty With Natural Kinematics; a Prospective Multicenter Study to Confirm the Safety and Efficacy of the InDx Implant
NCT06467760 ·Status: RECRUITING ·Phase: NA
-
Discovery Elbow Long-Term Survivorship
NCT01308463 ·Status: TERMINATED
-
Arthrex Eclipse™ Shoulder Prosthesis
NCT01790113 ·Status: TERMINATED ·Phase: NA
-
Proof-of-concept Study With NVDX3 for Treatment of Distal Radius Fractures.
NCT05987033 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study
NCT03357445 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Prospective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -Launay
NCT06012656 ·Status: ACTIVE_NOT_RECRUITING
-
Study of Patient Outcomes 5 Years After Partial Knee Replacement
NCT01620892 ·Status: COMPLETED
-
Autologous Osteoblastic Cells Implantation to Early Stage Osteonecrosis of the Femoral Head
NCT02890537 ·Status: COMPLETED ·Phase: PHASE2
-
Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - Europe
NCT03566082 ·Status: COMPLETED
-
Birmingham Hip Resurfacing (BHR) Study: Implantation of a Hip Resurfacing Endoprosthesis
NCT00180206 ·Status: UNKNOWN ·Phase: PHASE4
-
A Multicenter Study to Evaluate Functional Outcome After Knee Replacement
NCT02494544 ·Status: TERMINATED ·Phase: NA
-
Evaluate the Safety and Effectiveness of the Polymotion Hip Resurfacing (PHR) System Compared to Total Hip Arthroplasty
NCT06792539 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Oxford Partial Knee Replacement. A Randomized Clinical Trial of Three Implant Types
NCT00679120 ·Status: UNKNOWN ·Phase: NA
-
PMCF Study of the CLS Brevius Stem With Kinectiv Technology
NCT03410940 ·Status: TERMINATED
-
INHANCE Stemless Reverse Shoulder IDE
NCT06323980 ·Status: RECRUITING ·Phase: NA