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Study identifier: NCT07099885 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Simple Urine Composition-based Personalized Algorithm for Effective Congestion Relief in Decompensated Heart Failure

Condition: Acute Heart Failure (AHF) · Congestion, Venous  ·  Sponsor: Wroclaw Medical University

PhaseNA
Planned participants90
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The aim of this study is to evaluate the effectiveness of loop diuretic adaptative algorithm that is based on machine learning, urine output prediction tool, in decongestion of acute heart failure patients. A total of 90 patients will be enrolled in the study. Of these, 45 will be assigned to the algorithm-based intervention group, while the remaining 45 will serve as the control group. In the control group, all decisions regarding diuretic therapy will be made solely by the attending physician, without the use of the algorithm. Patients will receive intravenous furosemide, with the initial dose determined by the attending physician. Two hours after administration of the diuretic, a spot urine sample will be collected to measure sodium and creatinine concentrations. Based on these values, the 6-hour urine output will be estimated using the machine learning, urine output prediction tool (http://diuresis.umw.edu.pl). This estimate will guide the diuretic therapy plan for the first 24 hours of hospitalization. On the second day, the procedure will be repeated using the same methodology.

This description comes directly from the study's public registry record.

Talk to the study team

Jan Biegus, MD, PhD  ·  71 736 42 05  ·  jan.biegus@umw.edu.pl

Gracjan Iwanek, MD  ·  71 733 11 12  ·  gracjan.iwanek@student.umw.edu.pl

Always discuss trial participation with your own doctor first.

Locations (2)

Wroclaw Medical UniversityWroclaw, Dolnosląskie, PolandRecruiting
Wroclaw Medical UniversityWroclaw, Lower Silesian Voivodeship, PolandRecruiting

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Source record: clinicaltrials.gov/study/NCT07099885