20-Year shoulder surgery study tracks 1,733 patients for better recovery
NCT ID NCT02075775
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study follows over 1,700 people who had shoulder instability surgery to understand why some have ongoing pain, repeat dislocations, or need more surgery. Participants complete surveys about their recovery for up to 20 years. The goal is to find factors that lead to better or worse long-term results.
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.
- Participants
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1,733 people
The number who actually took part.
- Started
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Aug 2012
- Expected to finish
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Dec 2042
An estimate. End dates often move.
- 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.
Who is studied
Potential subjects are patients who are undergoing surgery of the labrum and/or capsule for shoulder instability
- Ages
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12 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: This is a prospective cohort study; there is no control group. Subjects that are included are all patients undergoing surgery for shoulder instability. Inclusion criteria: * Anterior, posterior, and inferior instability * Ages 12-99 * Open and arthroscopic repair * Revision of a previous shoulder instability repair * Latarjet/bone augmentation Exclusion Criteria: * Workers compensation patients * Prisoners * Non-English speaker * Not mentally competent * Unable/unwilling to return for clinical follow-up * Arthroplasty patients * Rotator cuff tears * Fractures
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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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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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Hospital for Special Surgery
New York, New York, 10021, United States
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Ohio State University
Columbus, Ohio, 43221, United States
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Orthopedic Institute
Sioux Falls, South Dakota, 57105, United States
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UCSF Orthopedic Institute
San Francisco, California, 94158, United States
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University of Colorado
Boulder, Colorado, 80304, United States
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University of Iowa
Iowa City, Iowa, 52242, United States
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University of Kentucky
Lexington, Kentucky, 40536, United States
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University of Michigan
Ann Arbor, Michigan, 48109-0328, United States
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Vanderbilt University
Nashville, Tennessee, 37232-8774, United States
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Washington University
St Louis, Missouri, 63110, United States