Evaluation of Fibroscan® Performance in Diagnosing Acute Heart Failure in Patients Presenting to the Emergency Department

Recruiting N/A Interventional Study
Acute Heart Failure (AHF)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
100 (estimated)
Sponsor
Assistance Publique - Hôpitaux de Paris · Other
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About This Trial
Acute heart failure (AHF) is a major cause of acute dyspnea in emergency departments (EDs), driven primarily by venous congestion, which can lead to hepatic congestion and risk of subsequent liver dysfunction. Current diagnostic tools include clinical evaluation, biomarkers, and imaging (Chest X-Ray or echography), are often limited by delayed results, variability, and suboptimal accuracy in emerg…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patients ≥18 years 2. ED patients presenting with acute dyspnea and absence of any other obvious cause of dyspnea (for example pneumothorax, acute pneumonia, acute coronary syndrome, Covid) … 3. Social security affiliation (except AME) 4. Informed consent signed Exclusion Cr…
Contacts

Amélie VROMANT, Medical Doctor

+33617253512

amelie.vromant@aphp.fr

CONTACT

Yonathan FREUND, PU-PH

+33663549017

yonathan.freund@aphp.fr

CONTACT