NCT07222813Recruiting
Evaluation of Liver Stiffness Performance, by FibroScan®, to Detect Elevated Central Venous Pressure (CVP)
Performance of Liver Stiffness Measurement (LSM) by FibroScan® for the Diagnosis of Elevated Central Venous Pressure (CVP)
Source: ClinicalTrials.gov · Last updated 23 Sept 2026
Brief summary (registry, in English)
This is a pivotal, global, prospective, cross-sectional, multicentric clinical investigation designed to explore a non-invasive, reliable alternative to invasive, catheter-based hemodynamic assessments, which are associated with procedural risks and limited applicability in certain participant populations.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 149 (estimated)
- First submitted
- 17 Oct 2025
- Start date
- 23 Apr 2026
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- Echosens
- Diseases
- Heart failure
- NCT number
- NCT07222813
What you commit to
- Study type: Interventional
- Planned participants: 149
- From 23 Apr 2026 to the primary completion date, 31 Dec 2027
- 7 sites in 4 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Chronic liver disease (self-reported alcohol use \>14 drinks/week in females and \>21 drinks/week in males), positive hepatitis C virus serology, positive hepatitis B surface antigen, autoimmune hepatitis, hemochromatosis, or cholestatic disease)
- Heart transplantation
Other
- Inability to consent
- BMI \>40 kg/m2
- Fontan-type circulation
- Ascites
- Pregnancy, breastfeeding, or intent to become pregnant during the study
- Intent to donate/bank or retrieve eggs (ova, oocytes) or donate sperm during the study
Who the study is looking for
- Have read, understood, and signed the informed consent form (ICF)
- Be ≥18 years of age at the time of screening
- Have suspected or diagnosed acute or chronic HF and be scheduled to undergo right-sided cardiac catheterization
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (7)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Deutsches Herzzentrum der Charité (DHZC) - Klinik fuer Herz-, Thorax- und Gefaesschirurgie Coordinator of this site? Confirm its status | Berlin | Germany | Recruiting |
| Centre Hospitalier Universitaire (Chu) de Rennes - Hopital de Pontchaillou Coordinator of this site? Confirm its status | Rennes | France | Recruiting |
| Uniwersytet Medyczny im. Piastow Slaskich we Wroclawiu, Instytut Chorob Serca Coordinator of this site? Confirm its status | Wroclaw | Poland | Recruiting |
| Medical University of South Carolina Coordinator of this site? Confirm its status | Charleston | United States | Recruiting |
| University of Texas Southwestern Medical Center - Clinical Heart and Vascular Center - West Campus Building 3 Location Coordinator of this site? Confirm its status | Dallas | United States | Recruiting |
| Keck Medicine of USC-Norris Healthcare Center - Transplant Clinic Coordinator of this site? Confirm its status | Los Angeles | United States | Not yet recruiting |
| University of Minnesota Coordinator of this site? Confirm its status | Minneota | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.