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Assessment of Residual Congestion in Acute Decompensated Heart Failure

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults (≥18 years) admitted with ADHF.

• Clinical evidence of congestion during admission, indicated by ≥1 of the following: pitting peripheral edema, ascites, elevated jugular venous pressure, or radiologic/ultrasound evidence of pulmonary congestion.

• Treatment with ≥40 mg i.v. furosemide or equivalent dose loop diuretic during admission.

Locations
Other Locations
Denmark
Aarhus University Hospital - Department of Cardiology
RECRUITING
Aarhus
Copenhagen University Hospital, Amager and Hvidovre Hospital - Department of Cardiology
NOT_YET_RECRUITING
Copenhagen
Zealand University Hospital - Department of Cardiology
NOT_YET_RECRUITING
Roskilde
Contact Information
Primary
Kristoffer Berg-Hansen, MD, PhD
krisbe@rm.dk
+4560540700
Time Frame
Start Date: 2026-02-15
Estimated Completion Date: 2028-11-01
Participants
Target number of participants: 580
Treatments
Patients admitted for acute decompensated heart failure
Related Therapeutic Areas
Sponsors
Collaborators: Zealand University Hospital, Amager Hospital
Leads: Aarhus University Hospital

This content was sourced from clinicaltrials.gov