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Shoulder surgery showdown: to repair or not to repair the subscapularis?
NCT ID NCT03727490
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether repairing the subscapularis tendon during reverse shoulder replacement surgery leads to better short-term outcomes. A total of 102 adults having primary reverse shoulder arthroplasty took part. Half had the tendon repaired, half did not. The goal was to see if the repair made a difference in how patients felt and functioned after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- subscapularis tendon repair (surgical procedure)
- What this could lead to
- If repairing the tendon proves beneficial, it could become a standard part of reverse shoulder replacement to improve recovery.
- What could go wrong
- This is a small, completed trial focused only on short-term outcomes. The results may not apply to all patients or show long-term benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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102 people
The number who actually took part.
- Started
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Dec 2018
- Finished
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May 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults undergoing primary reverse shoulder arthroplasty Exclusion Criteria: * Adults without an intact subscapularis * Inflammatory arthritis * Revision surgery
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Washington University Department of Orthopaedic Surgery
St Louis, Missouri, 63110, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.