CONTAK RENEWAL 3 AVT

Status Completed

Clinical Trial Summary

The RENEWAL 3 AVT device is designed to treat patients suffering from HF, with a history of or at risk of developing atrial and ventricular arrhythmias

Clinical Trial Description

A clinical evaluation to:

- Confirm that there are no adverse interactions when Ventricular Tachyarrhythmia (ICD), Heart Failure (HF) and Atrial Tachyarrhythmia (AT) therapies are combined

- Confirm Cardiac Resynchronization Therapy (CRT) and Ventricular Tachyarrhythmia (ICD) therapy is delivered in the presence of atrial therapies

- Demonstrate the safety and effectiveness of atrial therapies in a heart failure population ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00158977
Study type	Interventional
Source	Boston Scientific Corporation
Contact
Status	Completed
Phase	Phase 3
Start date	November 2003
Completion date	February 2008

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