What this study is
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.
Study details
- Sponsor
- Indiana University
- Conditions
- Heterotaxy Syndrome · Congenital Heart Defects
- Enrolling
- 2,000 people
- Starts
- 2009-07
- Est. completion
- 2030-12
- Record
- View on ClinicalTrials.gov ↗
Who can join
Sex ALLHealthy volunteers Not acceptedYou may qualify if
- Subjects with heterotaxy and related congenital heart defects
- Family members of subjects with heterotaxy and related congenital heart defects
You can't join if
- Subjects without heterotaxy and related congenital heart defects
- Family members of subjects without heterotaxy and related congenital heart defects
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openIndiana University School of Medicine
Indianapolis, Indiana, United States
- Lindsey R Helvaty, BA, BS · Contact317-278-3020lhelvaty@iu.edu
- Stephanie M Ware, MD, PhD · Contact317-278-2807stware@iu.edu
Recruiting
Study team
Sponsor
Indiana University
Study ID 1403871897
Principal investigator
Stephanie M. Ware, MD, PhD
Indiana University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.