Trials / Terminated
TerminatedNCT01060293
Dopamine in Acute Decompensated Heart Failure II
Comparison of High-dose Furosemide, Low-dose Furosemide, and the Combination of Low-dose Furosemide and Low-dose Dopamine in Patients With Acute Decompensated Heart Failure
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 161 (actual)
- Sponsor
- Larissa University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
The aim of this study is to compare the effects of: 1. high-dose furosemide (HDF, 40 mg furosemide bolus IV, followed by continuous IV infusion of 20 mg/h for a total of 8 hours), 2. 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 3. 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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | High-dose furosemide | High-dose furosemide (HDF): 20 mg/h continuous IV administration for 8 hours |
| DRUG | Low-dose furosemide | Low-dose furosemide (LDF): continuous IV administration of 5 mg/h furosemide |
| DRUG | Low-dose furosemide combined with low-dose dopamine | Low-dose furosemide combined with low-dose dopamine (LDFD): continuous IV administration of 5 mg/h furosemide combined with 5 μg/kg/min dopamine for a total of 8 hours |
Timeline
- Start date
- 2009-07-01
- Primary completion
- 2013-12-01
- Completion
- 2013-12-01
- First posted
- 2010-02-02
- Last updated
- 2013-09-11
Locations
6 sites across 2 countries: United States, Greece
Source: ClinicalTrials.gov record NCT01060293. Inclusion in this directory is not an endorsement.