Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT05880173

SCREaning of Advanced Liver Fibrosis Using Non-Invasive Tests in General Population

Led by University Hospital, Angers · Updated on 2025-12-08

502

Participants Needed

6

Research Sites

175 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main objective of the study is to evaluate the pertinence of initiating screening for advanced hepatic fibrosis after a FIB4 result \> 2.67 automatically calculated in the local laboratory and followed by a specialized hepatic evaluation.

CONDITIONS

Official Title

SCREaning of Advanced Liver Fibrosis Using Non-Invasive Tests in General Population

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 70 years
  • Blood sample taken at a medical testing laboratory selected for the study
  • Blood tests with AST and ALT levels less than or equal to 300 IU/l
  • Platelet count between 50 G/l and less than 500 G/l
  • FIB4 blood test result greater than 2.67 from automatic calculation in the medical laboratory within the last 3 months
  • Signed informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Currently under specialized follow-up for chronic liver disease
  • Difficulty understanding the French language
  • Pregnant, breastfeeding, or recently given birth
  • Persons detained or restricted by judicial or administrative decision
  • Persons under legal protection
  • Persons unable to give informed consent
  • Not affiliated with a social security system

AI-Screening

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Trial Site Locations

Total: 6 locations

1

Chu Angers

Angers, France, 49000

Not Yet Recruiting

2

Chu Bordeaux

Angers, France, 49000

Not Yet Recruiting

3

Chu Grenoble Alpes

Grenoble, France

Actively Recruiting

4

Centre Hospitalier de Lens

Lens, France

Actively Recruiting

5

Hopital Saint Joseph

Marseille, France

Not Yet Recruiting

6

Chu Nancy

Nancy, France

Actively Recruiting

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Research Team

C

Clémence CANIVET, MD, PHD

CONTACT

M

Matthieu LE LAY

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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