BioBrace® Implant for Arthroscopic Repair of Full Thickness Rotator Cuff Tears
NCT05997381
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
This study aims to evaluate the safety and effectiveness of arthroscopic rotator cuff repair augmented with the BioBrace® Implant vs. arthroscopic rotator cuff repair alone in subjects requiring surgical intervention for a full-thickness rotator cuff tear.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Rotator Cuff Tears
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 40 to 70 years
- Sex
- All
- Healthy volunteers
- Accepted
- Sponsor
- CONMED Corporation
- Last updated on ClinicalTrials.gov
- April 23, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Connecticut · 1
- ConMed · New Haven, CT
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.