Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 18 and up

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

PhasePhase 4
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment436 (estimated)
SponsorUniversity of Aarhus
Academic / other
Locations1 site (Randers)
StatusRecruiting
StartedJune 30, 2026
Main results expectedSeptember 1, 2027
Study endsOctober 1, 2027
Registry record updatedJuly 6, 2026
Trial IDNCT07577596 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.