Clinical Trial

Cold and Compression After Rotator Cuff Repair (RCR)

Recruiting
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Summary
The purpose of this study is to compare pain score (Patient-Reported Outcomes Measurement Information System: PROMIS NRS Pain Subscale) between the control and cold/compression groups pre-surgically, daily after surgery for 14 days, then weekly after surgery for 3 months, and at 6 months post-surgery.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-01.
Trial Details
NCT Number NCT07516327
Lead Sponsor Ochsner Health System
Collaborators: BREG, Inc
Conditions High-grade Partial or Full Thickness Rotator Cuff Tears
Enrollment 90 participants
Start Date 2026-03-01
Primary Completion 2027-09-01 (estimated)
Study Completion 2029-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-04-14