Establishing the Genetic Profile of Multiple Hereditary Exostoses (HME) in Families of BC
NCT ID: NCT00473850
Last Updated: 2011-04-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
2000 participants
OBSERVATIONAL
1998-12-31
2023-03-31
Brief Summary
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Detailed Description
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To complete the genetic work up DNA analysis will be done on all available family members. This will entail obtaining a blood sample from each family member willing to partake in the study. These blood samples will be used only for the purpose of identifying abnormalities in the genes related to osteochondromas. The blood samples will be taken at British Columbia's Children's Hospital and processed there. DNA samples will be kept confidential.
Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
ALL
No
Sponsors
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Circle of Care
UNKNOWN
Vancouver Foundation
OTHER
Children's & Women's Health Centre of British Columbia
OTHER
University of British Columbia
OTHER
Responsible Party
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University of British Columbia
Principal Investigators
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Christine Alvarez, MD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Locations
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BC Children's Hospital
Vancouver, British Columbia, Canada
Countries
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Other Identifiers
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H98-70441
Identifier Type: -
Identifier Source: org_study_id
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