Heart Failure Clinical Trial

Nesiritide Infusion for the Treatment of Decompensated Heart Failure and Renal Dysfunction

Summary

The researchers hypothesize that the addition of nesiritide to standard therapy will prevent worsening of renal function in patients admitted to the hospital with decompensated heart failure and renal dysfunction relative to standard therapy alone.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Decompensated heart failure hospitalization with at least 1 symptom and 1 sign of elevated filling pressures
Admission estimated creatinine clearance =< 50 cc/min.

Exclusion Criteria:

Systolic blood pressure < 85 mm Hg
Cardiogenic shock
Volume depletion
Myocardial infarction, unstable angina within last 30 days
Significant valvular stenosis, hypertrophic/restrictive cardiomyopathy, or constrictive pericarditis
Chronic hemodialysis
Anticipated major procedure during hospitalization i.e. left heart catheterization, surgery, or transplantation
Enrolled in another research protocol within last 30 days.

Study is for people with:

Heart Failure

Phase:

Phase 2

Estimated Enrollment:

34

Study ID:

NCT00119691

Recruitment Status:

Completed

Sponsor:

Brigham and Women's Hospital

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There is 1 Location for this study

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Brigham and Women's Hospital
Boston Massachusetts, 02115, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 2

Estimated Enrollment:

34

Study ID:

NCT00119691

Recruitment Status:

Completed

Sponsor:


Brigham and Women's Hospital

How clear is this clinincal trial information?

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