Screening for Chronic Liver Diseases in General Population
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU de Montpellier | Montpellier | France |
More University Hospital, Montpellier 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 NCT06366425 on ClinicalTrials.gov ↗ ← All trials in France