Clinical Trial

Assessment of Residual Congestion in Acute Decompensated Heart Failure

Study acronym: VExUS-AHF
Recruiting
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Summary
DESIGN: A prospective, multicenter, observational cohort study including 580 patients admitted for acute decompensated heart failure (ADHF). Ultrasound assessment of congestion (VExUS and LUS) will be performed serially during admission: within 48 hours of admission, at the time diuretic therapy is switched from intravenous to oral, and on the day of discharge. The discharge assessment will serve as the primary predictor. Treating physicians will be blinded to all ultrasound findings. Patients will be followed for 90 days by telephone follow-up and chart review for the primary endpoint, with extended chart review at one year for selected secondary endpoints. AIMS: To determine whether combined ultrasound assessment of venous (VExUS) and pulmonary congestion (LUS) at discharge predicts heart failure readmission and all-cause mortality in patients hospitalized with ADHF. HYPOTHESIS: Abnormal VExUS and/or LUS findings at discharge are associated with a higher risk of heart failure readmission and all-cause mortality after 90 days.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-06-26.
Trial Details
NCT Number NCT07682298
Lead Sponsor Aarhus University Hospital
Collaborators: Zealand University Hospital, Amager Hospital
Conditions Acute Heart Failure (AHF), Decompensated Chronic Heart Failure
Enrollment 580 participants
Start Date 2026-02-15
Primary Completion 2028-06-01 (estimated)
Study Completion 2028-11-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-07