“Avoid Transvenous Leads in Appropriate Subjects”
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
Patients will be randomized to receive either a subcutaneous or transvenous ICD.
Avoid Transvenous Leads in Appropriate Subjects