Actively Recruiting
Subscap Reverse Shoulder Arthroplasty
Led by University of Maryland, Baltimore · Updated on 2025-06-25
118
Participants Needed
1
Research Sites
234 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The subscapularis is part of the rotator cuff and is release as part of a reverse shoulder replacement. The decision to repair this tendon is controversial. This research is being done to help determine if rotator cuff repair improves or hinders shoulder replacement. A worrisome but rare complication after shoulder replacement is dislocation. Rotator cuff repair may help reduce this risk. The repair may hinder some of the range of motion afterwards or could help with internal rotation strength. There is a chance that the repair doesn't matter at all. The goal of this study is to delineate outcomes after reverse shoulder arthroplasty with the respect to management of the subscapularis tendon. Further information about rotator cuff repair after reverse shoulder replacement can help define complications, potentially decrease OR time, and improve functional outcomes. A total of 148 patients will be enrolled and the duration of the study will be 5 years. All patients will be required to follow-up at 2¬-week, 6-week, 3-month, 6-month, 1-year, and 2-year post-operative marks. Any time information is collected for a study there is a small risk of breach of confidentiality. There are no monetary costs or payments associated with this study. You may or may not benefit by taking part in this study. There is no guarantee that you will receive direct benefit from your participation in this study. To be clear, participation in this study is completely voluntary.
CONDITIONS
Official Title
Subscap Reverse Shoulder Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 95 years
- Undergoing reverse shoulder arthroplasty for any reason, including revision surgery
You will not qualify if you...
- Irreparable subscapularis tendon as shown by MRI or CT scan with more than Grade I or II fatty infiltration
- Any history of fracture in the upper arm bone near the shoulder
- Any revision surgery involving bone loss in the upper arm near the shoulder
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Maryland School of Medicine
Baltimore, Maryland, United States, 21201
Actively Recruiting
Research Team
M
Mohit Gilotra, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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