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Recruiting NCT07031089

NCT07031089 City-Hospital Collaboration for Early Detection of Liver Fibrosis in Primary Care: A Secondary Prevention Project in the Grenoble Health Area

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Clinical Trial Summary
NCT ID NCT07031089
Status Recruiting
Phase
Sponsor University Hospital, Grenoble
Condition Liver Fibrosis
Study Type OBSERVATIONAL
Enrollment 150 participants
Start Date 2026-01-14
Primary Completion 2028-08-14

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Non-interventional study (RIPH category 3)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 150 participants in total. It began in 2026-01-14 with a primary completion date of 2028-08-14.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Cirrhosis and hepatocellular carcinoma (HCC) are responsible for 25,000 deaths per year in France. The main causes are excessive alcohol consumption, metabolic steatosis, and hepatitis B and C. Fibrosis, classified from F0 (absence of fibrosis) to F4 (cirrhosis), is the sole determinant of liver-related mortality, particularly from stage F3. The incidence of metabolic steatosis is increasing, associated with a rise in mortality from chronic liver diseases (CLD). CLDs, often asymptomatic, are diagnosed late, reducing patient survival. Recommendations exist for the screening of hepatic fibrosis in at-risk patients (alcohol, diabetes, metabolic syndrome). This screening relies on calculating the FIB-4 score (calculated from widely prescribed variables: AST, ALT, platelets, age), followed by Fibroscan® (a non-invasive test for hepatic fibrosis) if FIB-4 \> 1.3. A Fibroscan® result \<8kPa excludes advanced fibrosis, while a result \>9.6kPa suggests advanced fibrosis and ≥15kPa indicates cirrhosis. The appropriate care pathway includes a risk reduction program, a specialized consultation for patients with Fibroscan® ≥8kPa, and semi-annual screening for HCC in the case of cirrhosis. Indeed, it has been shown in a French cohort of patients with viral C cirrhosis that adherence to semi-annual screening is associated with better survival. Eligible patients are primarily seen in primary care, and INCA has published a recommendation intended for general practitioners to improve the screening of fibrosis \[13\]. However, FIB-4 is poorly known among general practitioners \[14\], and access to Fibroscan® remains limited \[15\], hindering the implementation of the recommendations. Therefore, a care pathway has been established in the Grenoble area, initiated by Professor Costentin, allowing access to Fibroscan® for patients in primary care, starting from 2022 at the CHU. The objective is to evaluate the completion of the pathway, particularly the management of MCF risk factors and referral to specialized consultation for patients with Fibroscan® ≥8 kPa.

Eligibility Criteria

Inclusion Criteria: * Patients aged 18 years or older * Having undergone a Fibroscan® at the CHU de Grenoble-Alpes or CPTS-SEG, requested by a primary care practitioner (general practitioner, non-hospital diabetologist, Asalée nurse), as part of the screening recommendations for liver fibrosis in the case of a FIB4 score \> 1.3 * With a result ≥ 8kPa * Between January 2023 and January 2026 Exclusion Criteria: * Patients who have expressed their opposition to participating in the study * Patients under guardianship or deprived of liberty * Patients with a known chronic liver disease who are being monitored at the time of the Fibroscan® procedure

Contact & Investigator

Central Contact

Anna Borowik, PhD

✉ aborowik@chu-grenoble.fr

📞 +33476769314

Frequently Asked Questions

Who can join the NCT07031089 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Liver Fibrosis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07031089 currently recruiting?

Yes, NCT07031089 is actively recruiting participants. Contact the research team at aborowik@chu-grenoble.fr for enrollment information.

Where is the NCT07031089 trial being conducted?

This trial is being conducted at Grenoble, France, Grenoble, France.

Who is sponsoring the NCT07031089 clinical trial?

NCT07031089 is sponsored by University Hospital, Grenoble. The trial plans to enroll 150 participants.

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