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Clinical Trial Summary

Quest for modifier genes associated with ventricular arrhythmias in presence of a cardiac sodium channel gene (SCN5A-delPhe1617) mutation.


Clinical Trial Description

In a large Dutch SCN5A founder population with malignant ventricular arrhythmias, the investigators aim to identify genetic modifiers by means of whole-exome sequencing and to establish a comprehensive genotype-phenotype correlation, focussing on clinical and cellular electrophysiological characteristics and neurocardiac modulation. ;


Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT02014961
Study type Interventional
Source Maastricht University Medical Center
Contact Rachel ter Bekke, M.D.
Phone +31433877098
Email rachel.ter.bekke@mumc.nl
Status Recruiting
Phase N/A
Start date April 2015
Completion date April 2025

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