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Racial Distribution of Heterotaxy Syndrome

NCT00485654 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2012-03-16

No results posted yet for this study

Summary

Heterotaxy syndrome is a heterogeneous disease that is the result of a failure of normal right-left lateralization of the abdominal and thoracic organs during development. The major clinical manifestations include intestinal malrotation, functional asplenia and complex cyanotic heart disease.

Hypothesis: There exists a yet, un-recognized, racial distribution in heterotaxy syndrome.

Conditions

  • Congenital Disorders

Sponsors & Collaborators

  • Children's Healthcare of Atlanta

    lead OTHER

Principal Investigators

  • Rose M Cummings, DO · Sibley Heart Center Cardiology at Children's Healthcare of Atlanta

Eligibility

Max Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1990-01-31
Primary Completion
2005-01-31
Completion
2008-02-29

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 NCT00485654 on ClinicalTrials.gov