Heart Failure Clinical Trial

Assessment of Biomarkers and Cardiorenal Syndrome in Acute Decompensated Heart Failure With Vasodilator Therapy

Summary

The purpose of this study is to determine whether Nesiritide is more effective than nitroglycerin in modifying inflammatory and neurohormonal biomarkers without renal toxicity when proper infusion duration is administered.

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Full Description

No additional details provided

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Eligibility Criteria

Inclusion Criteria:

At least 18 years of age.
Subject must be able to understand the potential risks and benefits associated with the study.
Baseline systolic blood pressure ≥ 90 mm Hg at the time of enrollment.
Clinical symptoms of dyspnea and laboratory admission BNP levels > 500 pg/mL.
Neither pregnant or breastfeeding at the time of enrollment.
Authorization of patient's enrollment by patient's medical provider.

Exclusion Criteria:

<18 years of age
Denies written informed consent
Pregnant or lactating.
Baseline systolic BP < 90 mmHg or cardiogenic shock
No symptoms of congestion or admission BNP < 500 pg/mL
Known allergy to E.coli-derived products, or any history of anaphylactic reactions to nesiritide.
Receiving dialysis at the time of enrollment.
Serum creatinine > 2.5 mg/dL at the time of enrollment.

Study is for people with:

Heart Failure

Phase:

Phase 4

Estimated Enrollment:

89

Study ID:

NCT00842023

Recruitment Status:

Completed

Sponsor:

Western University of Health Sciences

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There is 1 Location for this study

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Centinela Hospital Medical Center
Inglewood California, 90301, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 4

Estimated Enrollment:

89

Study ID:

NCT00842023

Recruitment Status:

Completed

Sponsor:


Western University of Health Sciences

How clear is this clinincal trial information?

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