Clinical Trial

Postoperative USG Control and Clinical Follow-up of Massive Rotator Cuff Tendon Ruptures

Enrolling by Invitation
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Record status
This record was last updated June 4, 2025 (before its estimated May 30, 2026 completion). Its status may not reflect the trial's current state.
Summary
This prospective observational study aims to investigate the tendon integrity and clinical outcomes following surgical repair of massive rotator cuff tears. Patients with preoperatively diagnosed massive tears, confirmed by MRI and scheduled for surgery, will be included. Tendon healing will be assessed using ultrasonography at postoperative 2 weeks, 3 months, 6 months, and 12 months. Clinical evaluation will be conducted using standardized scoring systems including ASES, UCLA Shoulder Score, VAS, and thresholds for MCID, SCB, and PASS. The primary outcome is the rate and timing of retears at 12 months and their correlation with functional recovery. The study also aims to identify prognostic factors affecting tendon survivability, such as age, tear size, and muscle quality. By combining imaging and clinical parameters, this study seeks to contribute to the optimization of postoperative follow-up and rehabilitation strategies in the treatment of massive rotator cuff tears.
Trial Details
NCT Number NCT07004218
Lead Sponsor Gazi University
Conditions Early Retears and Clinical Outcomes Following Surgical Repair of Massive Rotator Cuff Tears
Enrollment 40 participants
Start Date 2025-02-01
Primary Completion 2026-05-30 (estimated)
Study Completion 2026-07-30 (estimated)
Updated on ClinicalTrials.gov 2025-06-04