Viewing StudyNCT00221832



Ignite Creation Date: 2024-05-05 @ 12:03 PM
Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00221832
Status: UNKNOWN
Last Update Posted: 2010-01-13
First Post: 2005-09-14

Brief Title: Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases
Sponsor: Heidelberg University
Organization: Heidelberg University

Conditions & Keywords Data

Conditions:
Name
Arrhythmogenic Right Ventricular Dysplasia
Long QT Syndrome
Hypertrophic Cardiomyopathy
Keywords:
Name View
Brugada Syndrome View
Long QT Syndrome View
Hypertrophic cardiomyopathy View
arrhythmogenic right ventricular dysplasia View
Short QT Syndrome View