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.
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 5U34AR069201-02 NIH grant funded the preparatory work for the trial but not the trial itself.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
189
Arthroscopic rotator cuff surgery followed by physical therapy.
Physical therapy (without surgery).
University of California - San Francisco (UCSF)
San Francisco, California, United States
Western Orthopaedics
Denver, Colorado, United States
Shoulder Pain & Disability Index (SPADI)
SPADI is a composite pain and function measure. The scale range is from 0 to 100, with 0 being best, and 100 being worst.
Time frame: Study participants will be followed for 12 months
American Shoulder and Elbow Surgeons (ASES)
ASES is a pain and activity of daily living questionnaire. The range is from 0 to 100, with 0 being worst, and 100 being best.
Time frame: Study participants will be followed for 12 months
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University of Colorado - Denver
Denver, Colorado, United States
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Iowa City, Iowa, United States
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Lexington, Kentucky, United States
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Baltimore, Maryland, United States
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Boston, Massachusetts, United States
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Boston, Massachusetts, United States
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Ann Arbor, Michigan, United States
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St Louis, Missouri, United States
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