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Dopamine in Acute Decompensated Heart Failure (DAD-HF) Trial

Comparison of High-dose Furosemide Versus the Combination of Low-dose Furosemide and Low-dose Dopamine in Patients With Acute Decompensated Heart Failure

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00937092
Acronym
DAD-HF
Enrollment
300
Registered
2009-07-10
Start date
2009-01-31
Completion date
2012-07-31
Last updated
2010-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Heart Failure

Keywords

Heart Failure, Dopamine, Furosemide, Worsening Renal Function, Hypokalemia, Outcomes, Prognosis

Brief summary

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

Detailed description

Worsening renal function (WRF) and hypokalemia related to diuretic use for acute decompensated heart failure (ADHF) are common and portend poor prognosis. Low dose dopamine infusion improves renal perfusion. Whether dopamine infusion improves diuresis and/or reduces renal complication in ADHF is not known. 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) vs. 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, renal function, electrolyte balance, and 60-day post-discharge outcomes in patients hospitalized with ADHF.

Interventions

DRUGlow-dose dopamine + low-dose furosemide

low-dose furosemide combined with low-dose dopamine (LDFD, furosemide 5 mg/h plus dopamine 5μg/kg/min intravenously)

DRUGFurosemide

High-dose furosemide(HDF, furosemide 20 mg/h intravenously)

Sponsors

Larissa University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

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 * all candidate patients must be: * Age \>18 years old * on medical therapy with an ACE-inhibitor and/or a β-blocker * experiencing an acute decompensation of known chronic HF * Having baseline oxygen saturation \<90% on admission arterial blood gas

Exclusion criteria

* the investigators will exclude patients with: * 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

Design outcomes

Primary

MeasureTime frame
1-year mortality or rehospitalization (all-cause, cardiovascular, non-cardiovascular, and due to worsening heart failure).1-year

Secondary

MeasureTime frame
60-day mortality or rehospitalization (all-cause, cardiovascular, non-cardiovascular, and due to worsening heart failure).60 days post discharge

Countries

Greece

Contacts

Primary ContactFilippos Triposkiadis, MD
ftriposkiadis@yahoo.com+30 2410682821
Backup ContactGregory Giamouzis, MD
ggiamou@emory.edu+30 6937212670

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026