Actively Recruiting

Phase Not Applicable
Age: 18Years - 95Years
All Genders
Healthy Volunteers
NCT05344898

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

Age: 18Years - 95Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 95 years
  • Undergoing reverse shoulder arthroplasty for any reason, including revision surgery
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Maryland School of Medicine

Baltimore, Maryland, United States, 21201

Actively Recruiting

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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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