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Congenital Heart Disease Research Registry

NCT00757510 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 861

Last updated 2014-12-09

No results posted yet for this study

Summary

The Congenital Heart Disease Research Registry (CHDRR) is a program dedicated to understanding the etiology and improving the treatment of Congenital Heart Disease (CHD). This Registry will act as a central coordinating center for recruiting subjects with CHD and will provide infrastructure and guidelines for researchers studying the causes and treatment of CHD. Investigators working directly with the Registry will have access to biological, demographic and phenotype data from a significant pool of participants with CHD.

Conditions

  • Congenital Heart Disease

Sponsors & Collaborators

  • Emory University

    lead OTHER

Principal Investigators

  • Paul M Kirshbom, MD · Emory University

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2010-02-28
Completion
2010-02-28

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 NCT00757510 on ClinicalTrials.gov