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Clinical trial

Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases

NCT00221832 is registered in ClinicalTrials.gov with Heidelberg University as lead sponsor.

NCT NCT00221832
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Registry record

As filed in ClinicalTrials.gov.

Title
Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases
Lead sponsor
Heidelberg University
Phase
Observational
Overall status
Unknown status
Start date
October 31, 2003
Completion date
December 31, 2011
Enrollment
300 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

arrhythmogenic right ventricular dysplasia, hypertrophic cardiomyopathy, long qt syndrome