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Prognosis evaluation of antiviral therapy for patients with chronic hepatitis B in immune tolerance stage

Prognosis evaluation of antiviral therapy for patients with chronic hepatitis B in immune tolerance stage

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067999
Enrollment
Unknown
Registered
2023-02-02
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

hepatitis B

Interventions

Immune tolerance period antiviral group:None
Immune tolerance period without antiviral group:None
GP73 normal group:None
Abnormal GP73 group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. HBV DNA>= 1.00E+07 IU/ML; 2. Serum HBsAg positive for at least 6 months and HBeAg positive; 3. Serum ALT was normal or < 2 x ULN; 4. No liver cirrhosis was indicated by Fibroscan < 9.0kpa and liver color ultrasound within the last 3 months, or no obvious inflammatory necrosis or fibrosis was observed by liver histopathological examination within the last 1 year; 5. All patients can be treated initially or after treatment.

Exclusion criteria

Exclusion criteria: 1. Cirrhosis, tumor, connective tissue disease, etc.; 2. Exclude alcoholic liver, drug hepatitis, autoimmune hepatitis, hepatitis A vale, etc.; 3. Serious dysfunction of heart, lung, liver, kidney and other systems; 4. Subjects with serious mental illness, pregnancy or lactation; 5. Conditions that other researchers consider unsuitable for participating in the study.

Design outcomes

Primary

MeasureTime frame
HBVDNA quantification;

Secondary

MeasureTime frame
GP73;HBsAg quantification;HBeAg quantification;ALT quantification;

Countries

China

Contacts

Public ContactXueZhong Lei

West China Hospital of Sichuan University

18980601317@163.com+86 189 8060 1317

Outcome results

None listed

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