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Study of Genetic Risk Factors for Spina Bifida and Anencephaly

NCT00031122 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1100

Last updated 2010-10-05

No results posted yet for this study

Summary

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.

Conditions

  • Spina Bifida
  • Anencephaly

Interventions

OTHER

No Intervention

There is no intervention in this study

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    lead NIH

Principal Investigators

  • Laura E. Mitchell, Ph.D. · The Texas A & M University Health Science Center

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2000-09-30
Primary Completion
2011-09-30
Completion
2012-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00031122 on ClinicalTrials.gov