LifeVest Post-CABG Registry

Status Terminated

Clinical Trial Summary

This is a multi-center prospective registry of patients with an ejection fraction (EF) ≤ 35% following coronary artery bypass graft (CABG) surgery in order to test the hypothesis that wearable defibrillators (WD) will decrease overall mortality after discharge by decreasing arrhythmic death in this select population with high risk for sudden cardiac death (SCD). This is a pilot project to determine the feasibility of a larger-scale study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01448005
Study type	Observational
Source	Zoll Medical Corporation
Contact
Status	Terminated
Phase	N/A
Start date	February 2011
Completion date	October 2014

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