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ASSURE Study - Arrhythmia Single Shock DFT Versus ULV: Risk Reduction Evaluation With ICD Implantations

Tachyarrhythmia Clinical Trial

Official title:
Arrhythmia Single Shock DFT Versus ULV: Risk Reduction Evaluation With ICDs Study

Clinical Trial Summary

The ASSURE Study will evaluate shock conversion performance when programming the first shock of an implantable cardioverter-defibrillation (ICD) is based on an implant test consisting of either 1) a single induction of ventricular fibrillation (VF) and subsequent demonstration conversion success at 14 J or 2) an upper limit of vulnerability (ULV) test at 14 J.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00231426
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Completed
Phase Phase 4
Start date June 2003
Completion date November 2005
View Details
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