Evaluation Of Outcomes Following Rotator Cuff Repair Using the REGENETEN Bioinductive Implant

This prospective, single-arm, multicenter registry is being conducted to collect real world post-market data from patients who are undergoing rotator cuff repair using the REGENETEN◊ Bioinductive Implant System. The Registry will include up to 50 centers in the United Kingdom (UK), Europe, Australia, and up to 400 patients for the initial evaluation. Patients will be treated and evaluated according to standard medical care. Outcome data is collected up to 2 years post-surgery.

NCT Number	NCT06857084
Lead Sponsor	Smith & Nephew, Inc.
Conditions	Rotator Cuff Injuries
Enrollment	400 participants
Start Date	2020-10-01
Primary Completion	2029-12-31 (estimated)
Study Completion	2029-12-31 (estimated)
Updated on ClinicalTrials.gov	2026-06-01