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Clinical Trial Summary

Rotator cuff tears are one of the most common reasons to seek musculoskeletal care in the United States and one of the fastest growing ambulatory surgery procedures. However, data on comparison of operative versus non-operative treatment is lacking and urgently needed.


Clinical Trial Description

This is non-blinded, randomized controlled trial. Patients will be randomly assigned to either an operative or non-operative course of treatment and will be followed for 12 months from baseline. Aim 1: To compare pain and function in patients undergoing operative versus non-operative treatment of atraumatic rotator cuff tears at 12 months of follow-up Aim 2: To assess effects of rotator cuff tear size and age on comparative outcomes of operative versus non-operative treatments for atraumatic rotator cuff tears ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03295994
Study type Interventional
Source University of Texas Southwestern Medical Center
Contact Hemangi Dhole, MPH
Phone 2146450059
Email hemangi.dhole@utsouthwestern.edu
Status Recruiting
Phase N/A
Start date March 19, 2018
Completion date June 30, 2025

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