Clinical Trials Directory

Trials / Completed

CompletedNCT00737490

Does Echocardiographically Guided Ventriculo-Ventricular Optimization Yield a Sustained Improvement in Echocardiographic Parameters in Cardiac Resynchronization Therapy Patients? (DEVISE CRT)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Duke University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether using an echocardiogram (a painless test where ultrasound is used to see your heart) while using mild electrical stimulation from your own CRT-D device to stimulate the ventricles (the lower chambers of the heart) to squeeze one slightly earlier than the other will show a sustained increase your heart's productivity (Cardiac Output (CO)), following implantation of a Cardiac Resynchronization Device (CRT-D). We believe that squeezing some parts of the heart earlier than others may make the heart a stronger pump.

Conditions

Interventions

TypeNameDescription
OTHER"Sequential Arm" (Promote , model # 2207-36 or Atlas HF , model # V-343)Echocardiographically guided optimized device programming: specifically sequential BiV pacing. "Sequential Arm" Using one of the FDA approved St. Jude devices, depending on MD preference.
OTHER"Simultaneous Arm" (Promote , model # 2207-36 or Atlas HF , model # V-343)simultaneous BiV pacing. Using one of the FDA approved St. Jude devices, depending on MD preference.

Timeline

Start date
2005-06-01
Primary completion
2009-12-01
Completion
2011-07-01
First posted
2008-08-19
Last updated
2014-08-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00737490. Inclusion in this directory is not an endorsement.