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Rotator Cuff Surgical Outcomes in Women

NCT02725320 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 192

Last updated 2019-04-26

No results posted yet for this study

Summary

The overall purpose of this work is to use a prospective cohort study to examine patient-specific but shoulder-extrinsic factors and how they influence the results of rotator cuff surgery. There are undoubtedly many factors that play a role in patient outcome, however, this project will focus on three: the effect of gender on outcome, the effect of mood disorders and coping style on outcome, and the effect of patient height and reach on outcome after rotator cuff surgery. It is hypothesized that these factors will have a significant influence over outcomes.

Conditions

  • Injury of Shoulder Region
  • Rotator Cuff Syndrome

Sponsors & Collaborators

  • University of Calgary

    lead OTHER

Principal Investigators

  • Marlis Sabo, MD, FRCSC · University of Calgary

Eligibility

Min Age
35 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2020-12-31
Completion
2020-12-31

Countries

  • Canada

Study Locations

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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 NCT02725320 on ClinicalTrials.gov