Development of a New Method for Liver Stiffness Measurement Using FibroScan
Condition(s) studied
Investigational drug(s) / intervention(s)
Research FibroScan (FS): Patients #1 to #25: Exam 1: Examination with Research FibroScan. Exam 2: Examination with the Reference FibroScan at the same measurement point and with the same probe used for the Exam 1. Patients #26 to #75: Exam 1: Examination with the Research or Reference FibroScan. Exam 2: Examination with the Reference or Research FibroScan at the same measurement point and with the same probe used for the Exam 1. Patients #76 to #114: Exams 1 \& 2: 2 consecutive examinations with the Research or Reference FibroScan. Exams 3 \& 4: 2 consecutive examinations with the Reference or Research FibroScan at the same measurement point and with the same probe used for the Exams 1 \& 2.
Study summary
This is an European, prospective, interventional, multicenter clinical investigation that will take place in 2 French sites. 153 adults patients will be included. The study objective is to develop a new method for measuring liver stiffness using FibroScan.
Eligibility
Primary outcome measure(s)
- Reduced intra-examination dispersion of liver stiffness measurements with the new measurement method. — 24 months
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Groupe Hospitalier Nord Essonne - Site Paris- Saclay | Orsay | France | Recruiting |
| Hôpital Pitié-Salpêtrière | Paris | Île-de-France Region | Recruiting |
More Echosens trials in France
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 NCT06519331 on ClinicalTrials.gov ↗ ← All trials in France