Infusion of furosemide to see if a loading infusion helps remove fluid better in acute heart failure
Official title: Infusion of Furosemide to Improve Diuretic Efficiency in Acute Heart Failure (INFUSE-AHF)
Run by University of Aarhus · NCT07577596 · Data updated 2026-11-12
This study tests whether giving furosemide as a continuous infusion with a loading dose is better at removing excess fluid than giving it as bolus injections in adults with acute heart failure.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 436 (estimated) |
| Sponsor | University of Aarhus Academic / other |
| Locations | 1 site (Randers) |
| Status | Recruiting |
| Started | June 30, 2026 |
| Main results expected | September 1, 2027 |
| Study ends | October 1, 2027 |
| Registry record updated | July 6, 2026 |
| Trial ID | NCT07577596 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (≥18 years) hospitalized with acute heart failure and signs of fluid overload who are planned to receive IV furosemide for at least 3 days.
✕Probably not a fit
Patients with shock, needing inotropes/vasopressors, renal replacement therapy, pregnancy, or severe electrolyte disturbances may not benefit or be excluded.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
INFUSE-AHF is a multicenter, open-label randomized trial in Denmark comparing two intravenous strategies for furosemide in adults with acute heart failure and fluid overload. Participants are assigned 1:1 to receive continuous infusion preceded by a loading dose or bolus injections three times daily, with treatment through Day 4 and follow-up up to 30 days after the first dose. The trial aims to determine which method achieves effective fluid removal more efficiently while considering safety and tolerability. It is designed as pragmatic to reflect real-world practice, enrolling patients during hospitalization who require IV furosemide for at least 3 days. Outcomes focus on diuretic effectiveness, weight change, and clinical status.
Why it matters
Potential benefit: If successful, the preferred administration method could improve fluid removal and patient recovery in acute heart failure.
How similar studies have gone: Previous studies have not established a clear winner between infusion and bolus dosing, making this comparison novel for this condition.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Clinical diagnosis of acute heart failure with volume overload * At least 1 sign of volume overload * Anticipated intravenous furosemide treatment for at least 3 days * Age 18 years or older Exclusion Criteria: * Shock * Patient requiring treatment with inotropes or vasopressors * Current or planned use of renal replacement therapy or ultrafiltration * Patient with a renal transplant * Patients who are pregnant or breastfeeding * Severe hypokalaemia, defined as potassium less than 2.5 mmol/L, or severe hyponatremia, defined as sodium less than 125 mmol/L * Allergy to furosemide and its components
Where it's running
-
Department of Medicine, Randers Regional Hospital
Randers, Denmark Recruiting
Study contacts
- Study coordinator: Esben Merrild, MD
- Email: esbenmerrild@clin.au.dk
- Phone: +4522996026
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Characterizing phenotypes of acute heart failure
This project will try to see if heart function measures, imaging features (radiomics), and blood biomarkers can predict outcomes for adults hospitalized with acute heart failure, including cardiogenic shock.
-
Early finerenone treatment for hospitalized adults with acute heart failure and LVEF ≥40%
This trial will test whether starting finerenone early during hospitalization helps adults with acute heart failure who have a left ventricular ejection fraction of 40% or higher.
-
Intensive GDMT optimization for women after heart failure hospitalization
This study tests whether rapidly increasing and closely monitoring heart failure meds in women after hospitalization can reduce death or readmission within a year.
-
Using intra‑abdominal pressure and bedside ultrasound to guide decongestive treatment in heart failure
This trial will test whether using bladder pressure (intra‑abdominal pressure) measurements together with bedside ultrasound to guide IV loop diuretics helps people hospitalized with acute heart failure get rid of excess fluid more effectively than usual care.
-
Subcutaneous Lasix ONYU for at-home treatment of worsening heart failure
This test will see if giving Lasix through a small subcutaneous device at home relieves fluid overload in adults with worsening heart failure.
-
Investigating heart issues in COPD patients during hospital stays
This study is trying to see if sudden worsening of COPD can cause heart problems in hospitalized patients and how it affects their recovery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.