Clinical Trial - Genetics of Congenital Heart Disease - Congenital Heart Disease

Nationwide Children’s Hospital is now utilizing whole exome sequencing (WES), with the addition of more traditional genetic techniques such as chromosomal microarray or traditional linkage analysis, to identify genetic causes of familial and isolated CHD.

 

Study Type: Observational
Estimated Enrollment: 1000 participants
Observational Model: Family-Based
Time Perspective: Prospective
Official Title: Genetics Testing of Individuals and Families With Congenital Heart Disease
Actual Study Start Date: December 2009
Estimated Primary Completion Date: December 2025
Estimated Study Completion Date: December 2025

 

Contact

Contact: Vidu Garg, MD 614-355-5710   vidu.garg@nationwidechildrens.org

 

ClinicalTrials.gov Identifier: NCT01192048

 

For enrollment please visit www.clinicaltrials.gov.

* The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.