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Molecular Genetics of Heterotaxy and Related Congenital Heart Defects

NCT02432079 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2025-06-26

No results posted yet for this study

Summary

The goal of this study is to obtain specimens and data from individuals and their families with heterotaxy and related congenital heart defects in order to clarify the molecular genetics of this disorder. The knowledge gained from the analysis of this information will provide the basis for future genetic counseling as well as contribute to knowledge about the biology of normal and abnormal development of left-right anatomic asymmetry.

Conditions

  • Heterotaxy Syndrome
  • Congenital Heart Defects

Sponsors & Collaborators

  • Indiana University

    lead OTHER

Principal Investigators

  • Stephanie M. Ware, MD, PhD · Indiana University School of Medicine

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2030-12-31
Completion
2030-12-31

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 NCT02432079 on ClinicalTrials.gov