RecruitingNCT07682298

Assessment of Residual Congestion in Acute Decompensated Heart Failure


Sponsor

Aarhus University Hospital

Enrollment

580 participants

Start Date

Feb 15, 2026

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with acute heart failure (ahf) and decompensated chronic heart failure. The study is currently recruiting participants at 3 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(3)

Aarhus University Hospital - Department of Cardiology

Aarhus, Denmark

Copenhagen University Hospital, Amager and Hvidovre Hospital - Department of Cardiology

Copenhagen, Denmark

Zealand University Hospital - Department of Cardiology

Roskilde, Denmark

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NCT07682298


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