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Clinical Trial Summary

Background: The wearable cardioverter defibrillator (WCD) is an established treatment option for patients at high risk for ventricular tachycardia / ventricular fibrillation (VT/VF), either in whom this risk may only be temporarily present, or in patients at high risk for sudden cardiac death (SCD) or after VT/VF in whom an implantable cardioverter defibrillator (ICD is currently not possible for other reasons (infection, recent MI <40days, recent PCI/CABG < 3months etc.). Methods: Comprehensive registry including all patients in Austria who received a WCD in 2010-2016.


Clinical Trial Description

Observational study to describe WCD indications, event rates, inappropriate shock rates and follow up (including ICD rate, shock rate, morbidity and mortality) in all Austrian WCD patients ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02816047
Study type Observational
Source Medical University of Graz
Contact Daniel Scherr, Assoz. Prof.
Phone 004331638512544
Email daniel.scherr@medunigraz.at
Status Recruiting
Phase
Start date November 2014
Completion date March 2022

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