The purpose of the study is to compare standard, single chamber transvenous ICD to
sub-cutaneous ICD in occurrence of perioperative and long term device related complications
and failed appropriate clinical shocks and arrhythmic death.
Device: Implantable Cardioverter Defibrillator
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Locations near you
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Full eligibility criteria for NCT02881255
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Patient is ≥ 18 - 60 years old AND has a standard indication for ICD; OR
Patient is ≥ 18 years old AND has any one of the following present:
An inherited arrhythmia syndrome (i.e. Long QT, Brugada, ARVC, hypertrophic or
dilated cardiomyopathy, early repolarization syndrome, idiopathic ventricular
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