Development of a New Method for Liver Stiffness Measurement Using FibroScan

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorEchosens

About this trial

This is an European, prospective, interventional, multicenter clinical investigation that will take place in 2 French sites. 114 adults patients will be included. The study objective is to develop a new method for measuring liver stiffness using FibroScan.

Eligibility criteria

Qualifiers

Adult patients (≥ 18 years of age) followed in the hepatology or endocrinology department for liver disease, suspected liver disease or consequences of liver disease, all etiologies combined.

Adult patient able to give his written consent

Patient affiliated to the French Social Security system

Disqualifiers

Vulnerable patients

Patients with liver ascites

Patients with heart failure

Trial design

Treatments tested in this trial

  • Research FibroScan (FS)

Treatment groups

114 Participants
are divided into 1 treatment group

Sponsors and collaborators