Clinical Trials Directory

Trials / Completed

CompletedNCT00605631

The Prevention of Myocardial Enlargement and Dilatation Post Myocardial Infarction Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
105 (actual)
Sponsor
Boston Scientific Corporation · Industry
Sex
All
Age
18 Years – 100 Years
Healthy volunteers
Not accepted

Summary

This study is designed to evaluate the effect of pacing on post-MI patients.

Conditions

Interventions

TypeNameDescription
DEVICECardiac pacing using any Guidant/Boston Scientific Implantable ICD or CRT-D System and any Guidant/Boston Scientific Intracardiac Lead SystemNo 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.

Timeline

Start date
2005-05-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2008-01-31
Last updated
2017-04-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00605631. Inclusion in this directory is not an endorsement.