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NCT Number: NCT07727187

Hepatitis B Infection Surveillance

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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
  • Affiliation with national health insurance system or equivalent coverage

Exclusion criteria

  • 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
  • Individuals deprived of liberty, under guardianship or under conservatorship

Treatment and study plan

Primary outcomes

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

    Time frame: Baseline (at inclusion)

    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

Secondary outcomes

  1. Demographic characteristics of newly identified chronic HBsAg carriers

    Time frame: Baseline (at inclusion)

    age, sex, country of birth

  2. Virological characteristics of newly identified chronic HBsAg carriers

    Time frame: Baseline (at inclusion)

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

  3. Antiviral treatment eligibility and response

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

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

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

    Time frame: Baseline (at inclusion)

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

  5. Diagnostic performance of HBsAg thresholds, in combination with other virological markers for distinguishing HBeAg-negative chronic HBV infection from HBeAg-negative chronic hepatitis B

    Time frame: Baseline (at inclusion)

    HBsAg levels, HBe status and HBV DNA levels

  6. Characteristics of HDV infection

    Time frame: Baseline (at inclusion)

    ALT and AST levels, HBV DNA level, HBsAg and HBcrAg levels, HBe status, HBV genotype, severity of liver disease and proportion of patients treated with bulevirtide with or without pegylated interferon

  7. Genome sequence analysis and identification of HBV motifs associated with the severity of liver disease in HBV/HDV-coinfected patients

    Time frame: Baseline (at inclusion)

    Whole genome sequence analysis using next-generation sequencing technology

  8. Comparison with previous French cohort data (2008-2012)

    Time frame: Baseline (at inclusion)

    Evolution of clinical, biological and demographical characteristics of participants enrolled between 2008 and 2012

  9. Biobank collection

    Time frame: Baseline (at inclusion)

    Collection and storage of whole blood samples

  10. Clinical performance of ultra-sensitive HBcrAg assay (iTACT-HBcrAg)

    Time frame: Baseline (at inclusion)

    sensitivity, specificity, positive and negative predictive values

Study contacts

Contact information is provided by the study sponsor or research team.

Meriem Harrabi, PhD

CONTACT

[email protected]

+331 4981 4845

Stéphane Chevaliez, PhD

CONTACT

[email protected]

+33 1 4981 2828

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

National Surveillance of Patients With Chronic Hepatitis B (±D) From Expert/Reference Hepatology Centers (FPRH), Hepatology Departments in General Hospitals (ANGH), and the Virology and Medical Pharmacology Network (ANRS-MIE)

Acronym: HEPB-SURVEY

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Jul 27, 2026
Registry last updated
Jul 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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