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Assessment of Weber Humeral Derotational Osteotomy Using CT Scan

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00358904
First Posted: August 1, 2006
Last Update Posted: April 27, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of British Columbia
  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

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

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: Dr. William Regan, University of British Columbia
ClinicalTrials.gov Identifier: NCT00358904     History of Changes
Other Study ID Numbers: C05-0678
First Submitted: July 28, 2006
First Posted: August 1, 2006
Last Update Posted: April 27, 2011
Last Verified: April 2011

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