Assessment of Weber Humeral Derotational Osteotomy Using CT Scan

This study has been completed.
Sponsor:
Information provided by:
University of British Columbia
ClinicalTrials.gov Identifier:
NCT00358904
First received: July 28, 2006
Last updated: April 26, 2011
Last verified: April 2011
  Purpose

Subjects who have had the Weber osteotomy for Hill-Sachs lesions will have CT of Both shoulders. Amount of rotation in operative shoulder will be compared to contralateral. QOL will be assessed


Condition
Hill Sachs

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Assessment of Weber Humeral Derotational Osteotomy Using CT Scan

Resource links provided by NLM:


Further study details as provided by University of British Columbia:

Estimated Enrollment: 20
Study Start Date: May 2006
Study Completion Date: April 2011
Primary Completion Date: April 2011 (Final data collection date for primary outcome measure)
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Subjects who have had the Weber osteotomy for Hill-Sachs lesions.

Criteria

Inclusion Criteria:

  • Subjects who have had the Weber osteotomy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00358904

Locations
Canada, British Columbia
Vancouver General Hospital, Orthopaedics Dept.
Vancouver, British Columbia, Canada
Sponsors and Collaborators
University of British Columbia
Investigators
Principal Investigator: William Regan, MD The University of British Columbia
  More Information

No publications provided

Responsible Party: Dr. William Regan, University of British Columbia
ClinicalTrials.gov Identifier: NCT00358904     History of Changes
Other Study ID Numbers: C05-0678
Study First Received: July 28, 2006
Last Updated: April 26, 2011
Health Authority: Canada: Health Canada

Keywords provided by University of British Columbia:
Hill Sachs
Weber osteotomy
shoulder dislocation

ClinicalTrials.gov processed this record on April 15, 2014