Trials / Enrolling By Invitation
Enrolling By InvitationNCT07226388
Pyrocarbon Hemiarthroplasty Versus Total Shoulder Arthroplasty for the Treatment of Glenohumeral Osteoarthritis
Hemiarthroplasty Versus Total Shoulder Arthroplasty for the Treatment of Glenohumeral Osteoarthritis: The Impact of Modern Implant Options
- Status
- Enrolling By Invitation
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 74 (estimated)
- Sponsor
- Washington University School of Medicine · Academic / Other
- Sex
- All
- Age
- 40 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This is a multi-center study assessing postoperative outcomes associated with hemiarthroplasty with pyrocarbon (hPYC) versus anatomic total shoulder arthroplasty (aTSA). Once eligibility criteria is met, the subject will be randomized to one of the two study arms. Subjects will be followed for ten years. Clinical and patient-reported outcome measures (PROMs) will be assessed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Hemiarthroplasty with pyrocarbon | Hemiarthroplasty with pyrocarbon |
| DEVICE | Anatomic total shoulder arthroplasty | Anatomic total shoulder arthroplasty |
Timeline
- Start date
- 2026-02-03
- Primary completion
- 2039-02-01
- Completion
- 2040-02-01
- First posted
- 2025-11-10
- Last updated
- 2026-02-19
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07226388. Inclusion in this directory is not an endorsement.