Heart Failure Clinical Trial

Prospective Randomized Evaluation of an Ultra Conservative Approach to Implantable Defibrillator (ICD) Programming in Patients With a Left Ventricular Assist Device (LVAD).

Summary

We propose to study a strategy empirically applied for the past 6 months at a high volume LVAD center (Vanderbilt Heart and Vascular Institute). This utilizes an ultra conservative device programming strategy to maximize battery longevity, avoid inappropriate implantable cardioverter defibrillator (ICD) therapy, improve quality of life through reduction in overall shock burden, and potentially avoid unnecessary device generator changes prior to transplant. Avoiding CIED (cardiac implantable electronic device) change out device procedures prior to transplant is desirable.

View Eligibility Criteria

Eligibility Criteria

Inclusion:

Age ≥ 18
Advanced Heart Failure
Scheduled for Heartmate II LVAD implant
With existing ICD

Exclusion:

-Age < 18

Study is for people with:

Heart Failure

Estimated Enrollment:

80

Study ID:

NCT01977703

Recruitment Status:

Completed

Sponsor:

Vanderbilt University Medical Center

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There is 1 Location for this study

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Vanderbilt University
Nashville Tennessee, 37232, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

80

Study ID:

NCT01977703

Recruitment Status:

Completed

Sponsor:


Vanderbilt University Medical Center

How clear is this clinincal trial information?

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