Hepatitis B Infection Surveillance

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

France is a low-endemicity country for hepatitis B virus (HBV) infection. In 2016, the prevalence of chronic HBV infection in the general population was estimated at 0.3%, corresponding to more than 135,000 HBsAg-positive individuals, of whom 82% were unaware of their infection. Data on hepatitis D virus (HDV) infection remain limited; however, available studies suggest a prevalence of 6% to 10% among HBsAg-positive individuals. Despite current guideline recommendations, up to 35% of newly diagnosed HBsAg-positive patients between 2018 and 2022 were not screened for HDV infection.

The World Health Organization (WHO) targets for 2030 include a 90% reduction in the incidence of chronic viral hepatitis, a 65% reduction in hepatitis-related mortality, and treatment coverage for 80% of eligible diagnosed individuals. Achieving these goals will require strengthening HBV and HDV screening strategies and improving linkage to care and retention throughout the care cascade.

Objectives: The primary objective is to assess the severity of liver disease, including significant fibrosis (≥F2) and cirrhosis (F4), among adults newly diagnosed with chronic HBV infection (with or without HDV infection) at Expert/Reference Hepatology Centers and Hepatology or Infectious Diseases Departments.

The secondary objectives are to:

1. Describe demographic and virological characteristics of HBsAg-positive patients; 2. Determine the proportion of patients eligible for HBV treatment and evaluate treatment response at 6 and 12 months; 3. Assess the utility of novel virological markers for classifying patients according to phases of chronic HBV infection; 4. Evaluate HBsAg thresholds, in combination with other markers, for distinguishing HBeAg-negative chronic infection from HBeAg-negative chronic hepatitis; 5. Compare clinical and virological characteristics of HBV-monoinfected and HBV/HDV-coinfected patients; 6. Identify molecular signatures associated with liver disease severity; 7. Compare findings with those of a national cohort conducted 15 years earlier; 8. Collect biological samples for future analyses; 9. Assess the clinical utility of a highly sensitive HBcrAg assay. Method: This is a multicenter, observational study including all adults aged ≥18 years with chronic HBV infection, whether managed as outpatients or inpatients, who are newly referred to Expert/Reference Hepatology Centers or to Hepatology or Infectious Diseases Departments.

Conclusions: This study will generate updated national data on liver disease severity, treatment eligibility, and virological characteristics among adults newly diagnosed with chronic HBV infection in France.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or older

Chronic HBsAg carriage

First referral to participating expert/reference hepatology centers or hepatology/infectious diseases departments

Written informed consent obtained

Disqualifiers

Telephone-only referrals or medical record-only consultations

Telemedicine-only consultations

Inability or unwillingness to comply with study procedures

Inability to understand study objectives or procedures

Trial population

Adults with chronic hepatitis B surface antigen (HBsAg) carriage, defined as persistent HBsAg positivity for at least 6 months or HBsAg positivity in the absence of anti-HBc IgM antibodies.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,360 Participants
are grouped into 1 trial group
Group A: One including subjects >18-year-old with chronic HBV infection

Trial outcomes

Primary outcomes

1

Proportion of patients with significant fibrosis (METAVIR score ≥F2), including cirrhosis (METAVIR score F4)

Liver disease severity assessed by non-invasive methods (liver stiffness measurement, direct or indirect serum biomarkers, composite scores such as FIB-4) and/or liver biopsy. Significant fibrosis is defined as METAVIR score F2 or higher

Time frame
Baseline (at inclusion)

Secondary outcomes

1

Demographic characteristics of newly identified chronic HBsAg carriers

age, sex, country of birth

Time frame
Baseline (at inclusion)
2

Virological characteristics of newly identified chronic HBsAg carriers

HBe status, HBV DNA level, genotype, HBsAg level, HBcrAg level, HBV RNA level, HIV or HCV coinfections

Time frame
Baseline (at inclusion)
3

Antiviral treatment eligibility and response

ALT and AST levels, HBV DNA level, HBsAg level, HBe status and severity of liver disease

Time frame
Baseline (at inclusion), 6 months and 12 months
4

Performance of novel virological markers (HBcrAg level and HBV RNA level) in identifying patients at risk of disease progression

ALT and AST levels, HBV DNA level, HBsAg level, HBe status, severity of liver disease (METAVIR score), HBcrAg level and HBV RNA level

Time frame
Baseline (at inclusion)

Other outcomes

Sponsors and contacts

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