- Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears — Recruiting • Non-phase study • NCT05444465.
- REGENETEN implant may help patients return to daily activities faster than standard repair for partial rotator cuff tears.
Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
The purpose of the study is to assess whether the REGENETEN™ Bioinductive Implant allows patients to get back to their everyday activities quicker than if the tendon is repaired by the standard repair technique 'Completion and Repair' for surgically treating partial-thickness rotator cuff tears. Conditions: Rotator Cuff Injuries Interventions: Isolated Bioinductive Repair, Completion and Repair Lead Sponsor: Smith & Nephew, Inc. Planned Enrollment: 234 participants