The Prevention of Myocardial Enlargement and Dilatation Post Myocardial Infarction Study

NACompletedINTERVENTIONAL
Enrollment

105

Participants

Timeline

Start Date

May 31, 2005

Primary Completion Date

March 31, 2009

Study Completion Date

March 31, 2009

Conditions
Post Myocardial Infarction
Interventions
DEVICE

Cardiac pacing using any Guidant/Boston Scientific Implantable ICD or CRT-D System and any Guidant/Boston Scientific Intracardiac Lead System

No specific device model is required - any FDA-approved, market-released Guidant/Boston Scientific implantable ICD or CRT-D system and any FDA-approved, market-released Guidant/Boston Scientific intracardiac lead system may be implanted as part of MENDMI.

Trial Locations (1)

45219

Christ Hospital, Cincinnati

Sponsors
All Listed Sponsors
lead

Boston Scientific Corporation

INDUSTRY