Investigating aCute heArt failuRe Decongestion Guided by Lung UltraSonography
Condition(s) studied
Investigational drug(s) / intervention(s)
LUS decongestive strategy: LUS results are documented in the electronic case report form (eCRF) and converted into a common score ranging from absence of congestion to severe congestion. This generic congestion score will be communicated to the treating physician by the research personnel, along with a proposal to step-up, maintain, or step-down the decongestive therapy.
PE decongestive strategy: PE results are documented in the eCRF and converted into a common score ranging from absence of congestion to severe congestion. This generic congestion score will be communicated to the treating physician by the research personnel, along with a proposal to step-up, maintain, or step-down the decongestive therapy.
Study summary
The goal of this clinical trial is to investigate whether a lung ultrasonography (LUS)-guided decongestion strategy in adults hospitalized for acute heart failure (AHF) can improve patient-centered outcomes.
The main questions it aims to answer are:
* Does this strategy shorten the length of stay and reduce early hospital readmissions?
* Does this strategy improve patients' symptoms and quality of life ?
Researchers will compare LUS to physical examination (PE).
Eligibility
Primary outcome measure(s)
- DAOH-40 — 40 days from study inclusion
Number of days spent alive outside the hospital in a 40-day timeframe from study inclusion. This outcome ultimately evaluates number of days spent alive and nonhospitalized, simultaneously assessing (re)hospitalization, unplanned emergency visits and mortality
Trial sites (5)
| Facility | City | Region | Status |
|---|---|---|---|
| Trois-Chêne Hospital, Geneva Univesity Hospitals | Geneva | Canton of Geneva | Recruiting |
| Geneva University Hospitals | Geneva | Canton of Geneva | Recruiting |
| Inselspital, Universitätspital | Bern | Switzerland | Recruiting |
| Fribourg University Hospital | Fribourg | Switzerland | Recruiting |
| Ospedale Civico, Ente Ospedaliero Cantonale | Lugano | Switzerland | Terminated |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06465498 on ClinicalTrials.gov ↗ ← All trials in Switzerland