Status:
COMPLETED
Clubfoot DNA Repository
Lead Sponsor:
Texas Scottish Rite Hospital for Children
Conditions:
Clubfoot
Eligibility:
All Genders
1-75 years
Brief Summary
To build a DNA repository to enable participation in ongoing and future Clubfoot genetic linkage studies.
Detailed Description
Clubfoot is a birth defect that can occur alone (in isolation) or as a part of a disease like cerebral palsy (CP). Genetic linkage is a research tool in which DNA samples are tested for genetic landma...
Eligibility Criteria
Inclusion
- For a family to be included in this study there should be at least one person in the family affected with Idiopathic Talipes Equinovarus (or clubfoot). If the person satisfies this criterion, then the affected person and his/her parents are included in the study. If there are other individuals in the family who are also affected (e.g. a cousin), then these individuals are also invited to participate in the study along with their parents, siblings and all other family members that link the two affected individuals (e.g. grandparents).
Exclusion
- Inability to speak and read English or Spanish
- Should not have any other major birth defect (e.g. Heart defects, Downs Syndrome or cerebral palsy).
Key Trial Info
Start Date :
January 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 4 2017
Estimated Enrollment :
379 Patients enrolled
Trial Details
Trial ID
NCT00607191
Start Date
January 1 2008
End Date
May 4 2017
Last Update
May 9 2017
Active Locations (1)
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1
Texas Scottish Rite Hospital for Children
Dallas, Texas, United States, 75219