Molecular Genetics of Heterotaxy and Related Congenital Heart Defects

Recruiting now

Conditions studied: Heterotaxy Syndrome, Congenital Heart Defects

In brief

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.

Key facts

Study ID

NCT02432079

Run by

Indiana University

People needed

2000

Starts

2009-07-01

Expected to finish

2030-12-01

Last updated by the study team

2026-06-22

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects with heterotaxy and related congenital heart defects
• Family members of subjects with heterotaxy and related congenital heart defects

You may not qualify if…

• Subjects without heterotaxy and related congenital heart defects
• Family members of subjects without heterotaxy and related congenital heart defects

Where it is running

• Indiana University School of Medicine — Indianapolis, Indiana, United States (enrolling)

Full record on ClinicalTrials.gov

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