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Clinical Trial Summary

This study will evaluate the subscapularis repair versus non-repair during a reverse shoulder arthroplasty (RSA).


Clinical Trial Description

The primary objective of this study is to evaluate pain and function in patients undergoing RSA with or without subscapularis repair. This primary outcome will be measured by analysis of Constant scores at two years post-operative. Secondary objectives are to evaluate pain, function and imaging, between the two groups at each applicable time point. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05438914
Study type Interventional
Source Arthrex, Inc.
Contact Kelly A Ganz
Phone 1 (800) 933-7001
Email kelly.ganz@arthrex.com
Status Recruiting
Phase N/A
Start date November 14, 2022
Completion date September 14, 2025

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