MOON Shoulder Instability-Cohort of Patients Undergoing Operative Treatment.

NCT02075775 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1733

Last updated 2026-04-08

No results posted yet for this study

Summary

This project will be a multi-center, prospective longitudinal cohort for all patients undergoing primary shoulder instability surgery, excluding isolated SLAP repairs. We will be looking for risk factors for recurrent instability, revision surgery, and poor outcomes. Patients will be asked to complete the RAND-36, ASES, Shoulder Activity, EQ-5D and WOSI outcome measures, as well as demographic and socioeconomic information. Surgeons will complete a form after surgery with information on radiographic findings, physical exam, surgical findings, and the repair. Patients will wear a sling post-operatively, and follow standardized rehabilitation protocols, including physical therapy.

Patients will be sent outcome questionnaires at 2, 6, 10, and 20 years after surgery.

Conditions

  • Other Instability, Shoulder
  • Dislocations
  • Subluxations
  • Recurrent Dislocation of Shoulder Region

Sponsors & Collaborators

  • University of Michigan

    collaborator OTHER
  • University of California, San Francisco

    collaborator OTHER
  • University of Kentucky

    collaborator OTHER
  • Hospital for Special Surgery, New York

    collaborator OTHER
  • University of Colorado, Denver

    collaborator OTHER
  • Ohio State University

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • Orthopedic Institute, Sioux Falls, SD

    collaborator OTHER
  • Vanderbilt University

    collaborator OTHER
  • Brigham and Women's Hospital

    collaborator OTHER
  • Carolyn M Hettrich

    lead OTHER

Principal Investigators

  • Carolyn M Hettrich, MD, MPH · Brigham and Women's Hospital

  • Brian Wolf, MD, MS · University of Iowa

Eligibility

Min Age
12 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2032-12-31
Completion
2042-12-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02075775 on ClinicalTrials.gov