CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 50 enrolled
Drug / intervention
Furosemide Bolus +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07464249
NCT07464249N/ACompleted

Comparison of the Effectiveness of Bolus and Infusion Diuretic Therapy in the Management of Acute Heart Failure in Emergency Departments: a Randomised, Double-blind Clinical Study

Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey·interventional·Posted Mar 11, 2026·Updated Mar 11, 2026

In Brief

A clinical study evaluating Furosemide Bolus and Furosemide Continuous İnfusion for Acute Decompensated Heart Failure (ADHF). Completed, enrolled 50 participants across 1 site.

Detailed Summary

Acute decompensated heart failure (ADHF) is a clinical syndrome associated with high morbidity and mortality rates. Current guidelines emphasize the importance of oxygenation and diuresis in the management of ADHF. However, there is no clear recommendation regarding whether diuretic therapy should be administered as intermittent bolus dosing or continuous infusion. The aim of this study was to compare the early efficacy of bolus versus continuous infusion diuretic therapy in the emergency department management of ADHF. In this single-center, prospective, randomized, double-blind, parallel-group clinical trial, patients aged ≥18 years presenting with ADHF and without known chronic kidney disease were randomized in a 1:1 ratio to receive either intermittent bolus therapy or continuous infusion therapy. Allocation concealment was ensured using opaque sealed envelopes. To maintain blinding, simultaneous placebo-like administrations were performed in both groups. The primary endpoint was total urine output at 2 and 4 hours. Secondary endpoints included changes in the internal jugular vein collapsibility index (JVCI) at 2 and 4 hours. Tertiary end point was spot urinary sodium at 2 and 4 hours.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesTurkey (Türkiye)
Collaborators--

Timeline

N/ACompletedFinished
20252026
First PostedMar 11, 2026
Enrollment StartApr 3, 2024
Primary CompletionSep 30, 2024
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 4 months ago

Interventions

Furosemide Bolusdrug

atients in this group received 2.5 times their usual daily diuretic dose administered as an intravenous bolus infusion

Furosemide Continuous İnfusiondrug

Patients in this group received 2.5 times their usual daily diuretic dose administered as an intravenous continious infusion