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Calmodulin Gene Mutations in Patients With Ventricular Arrhythmia of Unknown Origin - A Screening Study

Ventricular Tachycardia Clinical Trial

Official title:
Calmodulin Gene Mutations in Patients With Ventricular Arrhythmia of Unknown Origin - A Screening Study

Clinical Trial Summary

The aim of this study is to screen a well characterized patient population with ventricular tachycardia of unknown origin and treated with an implantable cardioverter-defibrillator (ICD) for mutations in the calmodulin genes.

Clinical Trial Description

Patients with ventricular tachycardia of unknown origin and treated with an implantable cardioverter-defibrillator (ICD) will be asked to participate in the study. For patients with results showing mutations in the calmodulin genes, family members (parents, siblings and children) will also be asked to participate in the study. For under age patients and relatives who agree to participate, informed consent will also be taken from their custodian. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01947543
Study type Observational
Source Region Örebro County
Contact
Status Withdrawn
Phase
Start date January 2017
Completion date April 2018
View Details
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