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SMS: Substrate Modification Study in Patients Getting an Implantable Cardioverter Defibrillator (ICD) — SMS  

Tachycardia, Ventricular Clinical Trial

Official title:
Substrate Modification Study in Patients Getting an ICD

Clinical Trial Summary

The present standard of care for the management of unstable ventricular tachycardia (VT) in the setting of chronic coronary artery disease is the placement of an implantable cardioverter defibrillator (ICD) after the initial episode, and radiofrequency ablation and/or antiarrhythmic medication in the event of recurrences causing frequent ICD interventions.

The primary purpose of this randomized study is the assessment of recurrences of unstable VT in patients who undergo ICD implantation plus substrate ablation after the initial episode compared to patients who only undergo ICD implantation. Thus the primary purpose is an improvement in the quality of life. A decrease in mortality is not a primary purpose of this study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00170287
Study type Interventional
Source Medtronic Bakken Research Center
Contact
Status Completed
Phase Phase 4
Start date May 2002
Completion date August 2011
View Details
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