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Sponsored by: |
University of British Columbia |
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Information provided by: | University of British Columbia |
ClinicalTrials.gov Identifier: | NCT00358904 |
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 |
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Hill Sachs |
Study Type: | Observational |
Study Design: | Cohort, Prospective |
Official Title: | Assessment of Weber Humeral Derotational Osteotomy Using CT Scan |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Probability Sample |
Subjects who have had the Weber osteotomy for Hill-Sachs lesions.
Inclusion Criteria:
Contact: Cheryl Davies | 604.875.5886 | cheryl.davies@vch.ca |
Canada, British Columbia | |
Vancouver General Hospital, Orthopaedics Dept. | Recruiting |
Vancouver, British Columbia, Canada | |
Contact: Cheryl Davies 604.875.5886 cheryl.davies@vch.ca | |
Principal Investigator: William Regan, MD |
Principal Investigator: | William Regan, MD | The University of British Columbia |
Responsible Party: | University of British Columbia ( Dr. William Regan ) |
Study ID Numbers: | C05-0678 |
Study First Received: | July 28, 2006 |
Last Updated: | September 24, 2008 |
ClinicalTrials.gov Identifier: | NCT00358904 |
Health Authority: | Canada: Health Canada |
Hill Sachs Weber osteotomy shoulder dislocation |
Dislocations Shoulder Dislocation |