Spina Bifida Clinical Trial
— SBRROfficial title:
The Spina Bifida Research Resource
Verified date | May 2009 |
Source | Office of Rare Diseases (ORD) |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Observational |
The purpose of this study is to describe the genetic contribution to the neural tube defects spina bifida (SB) and anencephaly (A), which includes identifying patients, defining the roles of certain genes, and studying gene-environment interactions.
Status | Active, not recruiting |
Enrollment | 1100 |
Est. completion date | September 2012 |
Est. primary completion date | September 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Families that include at least 1 member who has SB or who had a fetus affected with SB or anencephaly Exclusion Criteria: - Have an NTD (SB or anencephaly) as a component of an identified syndrome - Families of individuals who have diagnoses other than SB or anencephaly |
Observational Model: Family-Based, Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
United States | The Texas A & M University Health Science Center | Houston | Texas |
United States | The University of Pennsylvania School of Medicine | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Genetic loci identification and comparisons | After DNA sampling | No |
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