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Clinical Trial Summary

The overall goal of the study is to determine if repairing the subscapularis tendon during primary reverse shoulder arthroplasty effects short-term patient outcomes. The study is a patient blinded randomized controlled trial that is currently enrolling.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03727490
Study type Interventional
Source Washington University School of Medicine
Contact
Status Active, not recruiting
Phase N/A
Start date January 2017
Completion date January 2025

See also
  Status Clinical Trial Phase
Completed NCT03663283 - Liposomal Bupivacaine Interscalene Nerve Block in Shoulder Arthroplasty Phase 4
Not yet recruiting NCT04449146 - Scapular Positioning in Standing Position Using Sonography N/A
Terminated NCT04650698 - TXA in Revision Total Shoulder Arthroplasty Phase 4
Withdrawn NCT05341518 - Subscapularis Repair During Reverse Total Shoulder Arthroplasty N/A
Completed NCT03735173 - Comparing the Outcome of Cemented All-Polyethylene Pegged vs. Keeled Components Through a Subscapularis Tenotomy or a Subscapularis Peel N/A
Active, not recruiting NCT05499728 - Telerehabilitation After Shoulder Arthroplasty N/A
Terminated NCT03599336 - RSA vs. Nonop for 3 & 4-Part Proximal Humerus Fractures N/A