Heart failure is a disorder in which the heart does not pump blood adequately. This can lead to several serious problems, including reduced blood flow throughout the body, congestion of blood in the veins and lungs, and fluid accumulation in various organs and limbs. Diuretics are often used to address the problem of fluid accumulation, but the optimal dose and the amount of time over which to administer each dose are unclear. This study will compare high and low doses of diuretics administered over longer and shorter periods of time to determine the safest and most effective combination.
Heart failure is a common disorder in which the heart cannot pump enough blood to meet the needs of the rest of the body. Heart failure symptoms include shortness of breath, swelling, and fatigue. Standard treatment for the swelling associated with heart failure includes the use of diuretic medications, such as furosemide, which cause urination and the removal of excess fluids in the body. Although furosemide has been used to treat heart failure patients for many years, it is still unclear how much of the drug to use, and over what time period the drug should be given. This study will evaluate whether furosemide treatment is safer and more effective when the drug is given in high doses versus low doses and in two to three separate doses versus one continuous infusion. Participants in this study will begin study procedures within the first 24 hours of their hospital admission for heart failure. Participants will be randomly assigned to receive one of the following four treatments: high dose furosemide via continuous intravenous (IV) infusion and placebo every 12 hours via IV bolus; low dose furosemide via continuous IV infusion and placebo every 12 hours via IV bolus; high dose furosemide every 12 hours via IV bolus and placebo via continuous IV infusion; and low dose furosemide every 12 hours via IV bolus and placebo via continuous IV infusion. Each participant will receive treatment for the first 72 hours of his or her hospital stay. Participants will answer questionnaires and undergo physical examinations and blood tests during the first 96 hours of hospitalization and again before hospital discharge or on Day 7, if that occurs first. Participants will be asked to return to their doctors 60 days following hospital discharge to evaluate their responses to treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
308
Q12 hours bolus
Continuous infusion
1x oral dose
2.5x oral dose
Morehouse School of Medicine
Atlanta, Georgia, United States
Brigham and Women's Hospital
Boston, Massachusetts, United States
Minnesota Heart Failure Network
Minneapolis, Minnesota, United States
Mayo Clinic
Rochester, Minnesota, United States
Duke University Medical Center
Durham, North Carolina, United States
Baylor College of Medicine
Houston, Texas, United States
University of Utah Health Sciences Center
Murray, Utah, United States
University of Vermont - Fletcher Allen Health Care
Burlington, Vermont, United States
Montreal Heart Institute
Montreal, Quebec, Canada
Patient Well Being, as Determined by a Visual Analog Scale
Global Visual Analog Scale Scale Range 0-7200; higher score is better
Time frame: Measured at 72 hours
Change in Serum Creatinine
Time frame: Measured at baseline and 72 hours
Change in Weight
Time frame: baseline and 96 hours
Proportion of Patients Free of Congestion
Time frame: Measured at 72 hours
Dyspnea, as Determined by Visual Analog Scales
Global Visual Analog Scale Scale Range 0-2400; higher score is better
Time frame: Measured at 24 hours
Change in Serum Creatinine
Time frame: baseline and 24 hours
Change in Cystatin C
Time frame: baseline and 72 hours
Change in Serum Creatinine
Time frame: baseline and 48 hours
Change in Serum Creatinine
Time frame: baseline and 96 hours
Change in Serum Creatinine
Time frame: baseline and day 7
Change in Serum Creatinine
Time frame: baseline and day 60
Patient Well Being, as Determined by a Visual Analog Scale
Global Visual Analog Scale Scale Range 0-2400; higher score is better
Time frame: Measured at 24 hours
Patient Well Being, as Determined by a Visual Analog Scale
Global Visual Analog Scale Scale Range 0-4800; higher score is better
Time frame: 48 hours
Dyspnea VAS
Dyspnea Visual Analog Scale Scale Range 0-4800; higher score is better
Time frame: 48 hours
Dyspnea VAS
Dyspnea Visual Analog Scale Scale Range 0-7200; higher score is better
Time frame: 72 hours
Change in Cystatin C
Time frame: baseline and day 7
Change in Cystatin C
Time frame: baseline and day 60
Change in Uric Acid
Time frame: baseline and 72 hours
Change in Uric Acid
Time frame: baseline and day 7
Change in Uric Acid
Time frame: baseline and Day 60
Change in B-type Natriuretic Peptide
Change in NTproBNP
Time frame: baseline and 72 hours
Change in NTproBNP
Time frame: baseline and Day 7
Change in NTproBNP
Time frame: baseline and Day 60
Presence of Cardiorenal Syndrome
Time frame: Within 72 hours
Treatment Failure
Treatment failure is defined as the patient met cardiorenal syndrome endpoint, worsening or persistent heart failure endpoint, patient died, or there was clinical evidence of overdiuresis requiring intervention within first 72 hours after randomization
Time frame: Within 72 hours
Net Fluid Loss
Time frame: Through 24 hours
Net Fluid Loss
Time frame: Through 48 hours
Net Fluid Loss
Time frame: Through 72 hours
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