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Active, not recruiting Not applicable

Screening for Chronic Liver Diseases in General Population

NCT06366425 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-09-11
Last updated
2026-06-22

Condition(s) studied

Fibrosis, Liver

Investigational drug(s) / intervention(s)

Blood sample then fibroscan

Blood sample then fibroscan: The patient takes a blood test if none less than 6 months old is available, including a complete blood count (CBC) and a hepatic check. The FIB-4 score will be calculated from this blood test. If the result of the FIB-4 test is greater than 1.3 the person will be contacted by the SELHV (Service Expert de Lutte contre les Hépatites Virales) of the University Hospital of Montpellier in order to schedule, if she wishes, a second non-invasive screening examination of liver fibrosis by Fibroscan.

Study summary

Improving the care of patients with liver diseases in primary care and will allow patients with chronic liver disease to benefit from a course appropriate care.

Eligibility

Sex
ALL
Min age
40 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 40 years * Without known liver pathologies * Having at least one risk factor for chronic liver disease: risky consumption of alcoholic beverages according to the AUDIT questionnaire, the presence of metabolic syndrome, diabetes or a risk factor for viral hepatitis B, D or C. Exclusion Criteria: * Fibroscan already performed in the last 12 months * Failure to collect express oral consent * Patient not affiliated with or not benefiting from a national health insurance scheme * Patient protected by law * Patient under guardianship or curatorship * Patient deprived of liberty * Pregnant or breastfeeding woman

Primary outcome measure(s)

  • Evaluation of the liver fibrosis screening acceptability (FIB-4) — During the inclusion assessment at day 1 (Visit 0)
    percentage of patients who agreed to a FIB-4 blood test among all included patients offered screening.
  • Evaluation of the liver fibrosis screening acceptability (FIB-4 and Fibroscan) — During the inclusion assessment at day 1 (Visit 0) and at 1 month (visit 1)
    percentage of patients who agreed to a FIB-4 blood test FIB-4 followed by Fibroscan (if FIB-4 score\>1.3) among all included patients offered screening.

Trial sites (1)

FacilityCityRegionStatus
CHU de Montpellier Montpellier France

Other trials for the same condition

Official registry record

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 NCT06366425 on ClinicalTrials.gov ↗ ← All trials in France