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Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease

NCT00005322 · Status: COMPLETED · Type: OBSERVATIONAL

Last updated 2016-09-28

No results posted yet for this study

Summary

To identify genes involved in the pathogenesis of congenital heart disease, including atrial septal defects (ASDs), paramembranous ventricular septal defects (VSDs), and atrioventricular canal defects (AVCDs).

Conditions

  • Cardiovascular Diseases
  • Heart Diseases
  • Defect, Congenital Heart
  • Heart Septal Defects, Atrial
  • Heart Septal Defects, Ventricular
  • Endocardial Cushion Defects

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    lead NIH

Principal Investigators

  • Ronald Lauer · University of Iowa

Eligibility

Max Age
100 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
1990-01-31
Completion
1998-12-31

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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 NCT00005322 on ClinicalTrials.gov