Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases

  • STATUS
    Recruiting
  • participants needed
    300
  • sponsor
    Heidelberg University
Updated on 7 November 2020
cardiomyopathy
syncope
hypertrophy
arrhythmogenic right ventricular dysplasia
brugada syndrome
short qt syndrome

Summary

The aim of this study is the identification of familial congenital arrhythmogenic disorders and their clinical follow-up.

Description

Molecular genetic screening in patients with: - supraventricular - ventricular arrhythmia - syncopes of unknown origin and/or suspicion of an arrhythmogenic origin - family members of patients with sudden cardiac death and aborted sudden cardiac death Examination of patients includes routine testing like electrocardiogram (ECG), sequential ECGs, exercise testing, invasive electrophysiological stimulation, cardiac magnetic resonance imaging, intravenous drug challenge for identification/exclusion of eg Brugada syndrome. Examples are patients with Long QT Syndrome, Short QT Syndrome, Brugada Syndrome, familial atrial fibrillation, WPW-syndrome, arrhythmias due to familial hypertrophic cardiomyopathy or arrhythmogenic right ventricular dysplasia. Blood samples are taken for further molecular genetic screening.

Details
Condition Long QT Syndrome, Arrhythmogenic Right Ventricular Dysplasia, Hypertrophic Cardiomyopathy
Clinical Study IdentifierNCT00221832
SponsorHeidelberg University
Last Modified on7 November 2020

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