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Nucleoside analogues improve virology response and immune control efficacy in chronic hepatitis B patients

Nucleoside analogues improve virology response and immune control efficacy in chronic hepatitis B patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071623
Enrollment
Unknown
Registered
2023-05-19
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Chronic hepatitis B

Interventions

low-level viremia group:Chronic hepatitis B patients who meet the criteria of hypoviremia are divided into three groups on a voluntary basis, one group: nucleoside analogues combined with technical dr
Group 2: Nucleoside analogues combined with dressing changes and polyethylene glycol interferon a- 2b (Pegbin)
Group 3: Nucleoside analogues combined with dressing change single us
Complete virology response group:CHB patients with complete virology response were divided into two groups on a voluntary basis, one group: NUCs technical drug+PegIFN a- 2b
Group 2: NUCs technical single use

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Clinical diagnosis of chronic hepatitis B 2. Age range from 18 to 60 years old, regardless of gender; 3. Patients who have been receiving NAs treatment for more than 1 year 4.TBil<2ULN 5. No contraindications to interferon treatment and willing to accept Peg-IFN a- 2b treatment, sign the informed consent form for interferon treatmen

Exclusion criteria

Exclusion criteria: 1. Patients with combined HAV, HCV, HDV, HEV infections, and autoimmune liver disease; 2. Pregnant and lactating women, as well as patients who are preparing to give birth recently; 3. Patients with liver cirrhosis 4. Have a history of serious heart disease, including unstable or uncontrolled heart disease within 6 months; 5. Have a history of mental illness; 6. Uncontrolled epilepsy; 7. Drunken or drug users who have not quit; 8. Uncontrolled diabetes, hypertension, thyroid disease, retinopathy, autoimmune disease, etc; 9. Total bilirubin>34umol/L; 10. Determine patients with past or current liver cirrhosis or liver cancer through liver ultrasound or liver hardness measurement; 11. Neutrophil count<2 × 109/L and/or platelet count<100 × 109 /L? 12. Other situations that the supervising physician deems unsuitable for enrollment

Design outcomes

Primary

MeasureTime frame
HBV DNA;HBsAg;

Secondary

MeasureTime frame
HBeAg;HBeAb;HBV RNA;

Countries

China

Contacts

Public ContactZhiwei Li

Shengjing Hospital of China Medical University

sy901015@sina.com+86 189 4025 1727

Outcome results

None listed

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