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NCT Number: NCT06525909

A Real-world Study of Staging and Grading of Clinical Immune Status in Chronic Hepatitis B

This is a prospective, multicentre observational study of Chronic Hepatitis B (CHB)in different clinical stages. We intend to compare the immune status of various types of CHB patients, and we propose to establish a staging and grading criteria for the immune exhaustion status of patients with CHB.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Tongji Hospital, Wuhan, Hubei, China

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About this study

Two groups were included in this study: untreated patients who met the staging subgroups according to Chinese Guidelines for the Prevention and Control of Chronic Hepatitis B, 2022 edition or HBsAg negativity(Group 1). The another is those who achieved HBV DNA suppression by NA(Group 2). Patients in Group 1 will be followed up once every six months, and in group 2 will be followed up once every three months. And patients treated or not treated will be followed up in the study. The treatment with NA or combined with interferon will be decided by the consensus of doctors and patients. This study does not intervene the treatment, but will register the clinical indicators. We follow up the patients at each follow-up time point, record the subjects' clinical indicators at each visit and obtained serum and PBMC specimens for further immune study after the consents of the patients.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Patients with CHB who were older than 18 years old and younger than 50 years old with HBsAg positivity more than 6 months;
  • Group 1 untreated group fulfils any one of the four natural history types of the Chinese Guidelines for the Prevention and Control of Chronic Hepatitis B, 2022.
  • Group 2 nucleos(t)ide-treated CHB patients are required to have sustained control of their HBV DNA (<100 IU/ml).

Exclusion criteria

  • Pregnancy status;
  • Has been diagnosed with compensated/lost compensated cirrhosis, hepatocellular carcinoma by imaging or other indicators;
  • Combined HAV, HCV, HEV infection, schistosomal liver disease, drug-induced liver injury, autoimmune hepatitis, alcoholic liver disease, severe fatty liver, HIV infection;
  • Being on immunosuppressants or immunomodulators or hormonal drugs or biological agents, etc;
  • previous history of oncology, organ transplantation, etc., history of alcoholism (>30 g/d for men, >20 g/d for women);
  • Inadequate follow-up time and inadequate clinical/laboratory information;
  • Combined heart, brain, kidney, lung and other organ insufficiency or combined endocrine and haematological system and other major diseases;
  • Comorbid serious psychiatric diseases including severe anxiety or depression;
  • Unwilling to participate in this study.

Treatment and study plan

Primary outcomes

  1. A preliminary exploration of staging and grading criteria for the state of immune

    Time frame: week 200

    The clinical characteristics, viral load and immune cells frequency (CD4+ or CD8+ T cells, etc) of CHB in different clinical stages will be studied.

Study contacts

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

Meifang Han, Doctor

CONTACT

[email protected]

862783662391

Qin Ning, Doctor

CONTACT

[email protected]

862783662391

Sponsors and collaborators

Lead sponsor

Tongji Hospital

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2028
First posted
Jul 29, 2024
Registry last updated
Jul 29, 2024

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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