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Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears

Exploring REGENETEN™ for partial shoulder tears in a clinical study.

Recruiting
18 years and older
All
Phase N/A

This study looks at a new way to help people heal from a shoulder injury called a "partial-thickness rotator cuff tear." The rotator cuff is a group of muscles and tendons that help your shoulder move. The study tests the REGENETEN™ Bioinductive Implant, a small device put in the shoulder, to see if it helps people get back to normal faster than usual surgery. This is compared to the usual method called "Completion and Repair." The study checks how well patients recover after 3 months. To join, you must be over 18, have a specific shoulder tear, and have tried other treatments for 3 months without success. You can't join if you have other shoulder problems, certain medical conditions, or have had recent shoulder surgery. You must also be able to attend all study visits and follow instructions.

  • Study Length: 3 months of follow-up.
  • Visits Needed: All required study visits must be attended.
  • Risks: May include standard surgery risks and implant-related issues.
Study details
    Rotator Cuff Injuries

NCT05444465

Smith & Nephew, Inc.

17 May 2025

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