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

Recruiting now · Not applicable

Conditions studied: Acute Heart Failure (AHF)

In brief

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 emergency settings. Fibroscan®, a non-invasive device originally designed to assess liver stiffness in chronic liver conditions, has shown potential in detecting liver congestion linked to heart failure. Studies have highlighted significant correlations between liver stiffness measurements (LSM) and markers of venous congestion, such as central venous pressure and adverse outcomes in heart failure patients. Preliminary findings suggest that LSM could provide rapid, bedside insights into systemic congestion, offering a promising avenue for improving diagnostic workflows in acute care. While prior research has mainly focused on chronic heart failure or small study populations, further investigation is needed to explore the utility of Fibroscan® in acute presentations of AHF within EDs. This could help address the limitations of existing diagnostic approaches and enhance patient management in time-sensitive environments.

Key facts

Study ID: NCT07449377
Run by: Assistance Publique - Hôpitaux de Paris
People needed: 100
Starts: 2026-04-02
Expected to finish: 2026-11-01
Last updated by the study team: 2026-06-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Patients ≥18 years
ED patients presenting with acute dyspnea and absence of any other obvious cause of dyspnea (for example pneumothorax, acute pneumonia, acute coronary syndrome, Covid) …
Social security affiliation (except AME)
Informed consent signed

You may not qualify if…

Known chronic liver disease, defined by a Prothrombic time of < 50%, or any former diagnosis of liver fibrosis.
No skin wounds in the abdominal area on which the Fibroscan® will be used
History of liver transplantation
eGFR <30 mL/min
Patient under legal protection measure (tutorship or curatorship) and patient deprived of freedom
Pregnancy and breastfeeding
Participation in another interventional trial

Where it is running

Name: Emergency Department Hospital Pitié-Salpêtrière, APHP — Paris, France (enrolling)

Full record on ClinicalTrials.gov

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