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The study on immunological mechanism of clinical cure of hepatitis B based on single cell RNA sequencing

The study on immunological mechanism of clinical cure of hepatitis B based on single cell RNA sequencing

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100908
Enrollment
Unknown
Registered
2025-04-17
Start date
2024-01-02
Completion date
Unknown
Last updated
2025-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic hepatitis B

Interventions

Clinical cure group obtained from NAs treatment:None
Clinical cure group achieved by combining NAs with Peg-IFNa therapy:None
Hepatitis B spontaneous clearance group:None
Treatment with nucleoside analogues without clinical cure group:None
Combining NAs with Peg-IFNa therapy without clinical cure group:None
Untreated without clinical cure group:None

Sponsors

Department of Infectious Diseases, Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with previously diagnosed chronic hepatitis B who have achieved clinical cure without drug treatment or after NAs/Peg-IFNa treatment. Patients diagnosed with chronic type B and treated with NAs for more than 48 weeks, and the treatment duration is less than half a year different from that of the clinically cured patients, but no clinical cure has been obtained. Clinical cure requires four requirements: (1) HBsAg persistently undetectable, HBeAg negative transfection, with or without HBsAb; (2) HBV DNA below the lower limit of detection; (3) Liver function remained normal; (4) There were no other lesions in liver histology detected by other methods such as ultrasound. The diagnostic criteria refer to the Guidelines for the Prevention and Treatment of Chronic Hepatitis B (2022 Edition)

Exclusion criteria

Exclusion criteria: (1) Combined with other hepatitis virus infections; (2) Combined with drug-induced liver injury, alcoholic liver disease, non-alcoholic fatty liver disease, autoimmune liver disease, etc.; (3) Combined with immunodeficiency diseases such as HIV; (4) Patients with malignant tumors of the liver or other sites; (5) Pregnant or lactating patients.

Design outcomes

Primary

MeasureTime frame
peripheral blood mononuclear cell ;

Countries

China

Contacts

Public ContactZhang Dazhi

The Second Affiliated Hospital of Chongqing Medical University

zhangdazhi_1014@163.com+86 134 5238 2818

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026