Heart Failure Clinical Trial

Dopamine in Acute Decompensated Heart Failure II

Summary

The aim of this study is to compare the effects of 1) high-dose furosemide, 2) low-dose furosemide, and 3) low-dose furosemide combined with low-dose dopamine on diuresis, clinical status, renal function, electrolyte balance, length of stay, and 60-day post-discharge outcomes in patients hospitalized with acute decompensated heart failure.

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Full Description

The aim of this study is to compare the effects of:

high-dose furosemide (HDF, 40 mg furosemide bolus IV, followed by continuous IV infusion of 20 mg/h for a total of 8 hours),
low-dose furosemide (LDF, 40 mg furosemide bolus IV, followed by continuous IV infusion of 5 mg/h furosemide for a total of 8 hours), and
low-dose furosemide combined with low-dose dopamine (LDFD, 40 mg furosemide bolus IV, followed by continuous IV infusion of 5 mg/h furosemide plus 5μg/kg/min dopamine for a total of 8 hours) on diuresis, perceived dyspnea, renal function, electrolyte balance, total length of stay, and 60-day post-discharge outcomes in patients hospitalized with ADHF.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

patients with New York Heart Association (NYHA) functional class IV heart failure according to the American Heart Association (AHA) classification, namely dyspnea on minimal exertion or rest dyspnea, orthopnea, and paroxysmal nocturnal dyspnea,
signs of congestion (third heart sound or pulmonary rales on physical examination),
pulmonary congestion on chest x-ray,
serum B-type natriuretic peptide levels > 400 pg/ml or NT-proBNP > 1500 pg/ml,
echocardiographic documentation of systolic or diastolic dysfunction,
age >18 years old,
on medical therapy with an ACE-inhibitor and/or a β-blocker,
experiencing an acute decompensation of known chronic HF,
baseline oxygen saturation <90% on admission arterial blood gas

Exclusion Criteria:

acute de novo HF;
severe renal failure (serum creatinine >200 μmol/L or GFR <30 ml/min/1.73m2)
admission systolic blood pressure <90 mm Hg;
severe valvular disease;
known adverse reactions to furosemide or dopamine;
HF secondary to congenital heart disease;
a scheduled procedure with a need for IV contrast dye;
a scheduled cardiac surgery within 6 months

Study is for people with:

Heart Failure

Phase:

Phase 4

Estimated Enrollment:

161

Study ID:

NCT01060293

Recruitment Status:

Terminated

Sponsor:

Larissa University Hospital

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There are 2 Locations for this study

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Division of Cardiology, Emory University Hospital
Atlanta Georgia, , United States
The Cleveland Clinic Foundation
Cleveland Ohio, , United States
First Department of Cardiology, University of Athens
Athens Attiki, , Greece
Department of Cardiology, Volos General Hospital
Volos Magnesia, 382 2, Greece
Department of Cardiology, Larissa University Hospital
Larissa , 411 1, Greece
AHEPA University Hospital
Thessaloniki , , Greece

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 4

Estimated Enrollment:

161

Study ID:

NCT01060293

Recruitment Status:

Terminated

Sponsor:


Larissa University Hospital

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