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Increase the Clinical Cure Rate with Immunomodulatory/ Antiviral based Combination Therapy in HBeAg Negative Chronic Hepatitis B Patients

Increase the Clinical Cure Rate with Immunomodulatory/ Antiviral based Combination Therapy in HBeAg Negative Chronic Hepatitis B Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016170
Enrollment
Unknown
Registered
2018-05-16
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Chronic (viral) hepatitis B

Interventions

Sponsors

The First Affiliated Hospital, College of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. signed the informed consent form; 2. HBsAg (+),and HBsAg titers less than or equal to 1500 IU / mL; 3. aged 18-65 years old; 4. HbeAg negative and ALT=2 times the upper limit of normal(ULN) or liver biopsy showing above G2 inflammation, and HBVDNA>=10^4 copies/mL (or HBVDNA >=2*10^3 IU/mL); (or HBeAg clearance after antiviral treatment with nucleoside (acid) analogues in chronic hepatitis B patients with HBeAg-positive); 5. pregnancy test should be negative in childbearing age female patients before the treatment, and can take effective contraceptive measures during treatment and within six months after the end of treatment. Including female and male patients female companion.

Exclusion criteria

Exclusion criteria: 1. patients with a allergy histroy of interferon, nucleoside (acid)antiviral drugs, colony stimulating factor or hepatitis B vaccine; 2. patients with HAV, HCV, HDV, HEV, HIV co-infection; 3. patients with cirrhosis or a Child-Pugh score of more than 7 points; 4. patients with medical history or evidence of other liver disease (such as autoimmune liver disease, alcoholic liver disease, nonalcoholic fatty liver disease, drug-induced hepatitis, Wilson degeneration, etc.); 5. pregnant or lactating women; 6. patients with a history of alcoholism or drug abuse within one year before screening into the trail; 7. neutrophil count <1.5 × 10^9/L or hemoglobin <100 g / L or platelet count <80 x 10^9/L; 8. patients with serum creatinine higher than normal limit during screening; 9. patient with a histroy of severe heart, brain, kidney, retina, muscle or other vital organs disease; 10. patients with history of mental illness or a family history of mental illness, or Hamilton depression scale score = 7 points; 11. patients with endocrine system or autoimmune disease history, such as thyroid disease, diabetes, systemic lupus erythematosus, sarcoidosis, autoimmune thrombocytopenic purpura, etc.; 12. Chronic diseases that require long-term treatment, such as hypertension, diabetes, chronic obstructive pulmonary disease, etc.; 13. patients with malignancy; 14. B-ultrasonography detected suspicious liver malignancies in the screening group, or alpha-fetoprotein was greater than 100 ng/mL; or alpha-fetoprotein could not be stable within 3 months before the test; 15. History of important organ transplants; 16. Researchers consider other diseases that are not suitable for the study.

Design outcomes

Secondary

MeasureTime frame
Physical examination;Liver function test;

Primary

MeasureTime frame
HBV-DNA;HBV M test;Liver pathology examination;

Countries

China

Contacts

Public ContactYida Yang

The First Affiliated Hospital, College of Medicine, Zhejiang University

yangyida65@163.com+86 57187236731

Outcome results

None listed

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