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A prospective, multicenter study for Evaluating Multi-Regimens of Adding on or Switching to PegIFN-alfa-2b to CHB NUCs treated Patients

A prospective, multicenter study for Evaluating Multi-Regimens of Adding on or Switching to PegIFN-alfa-2b to CHB NUCs treated Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021083
Enrollment
Unknown
Registered
2019-01-27
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

HBV

Interventions

Case series:nucleoside (acid) analogues after 24 weeks of sequential or combined treatment with pegylated interferon alfa-2b

Sponsors

First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Adults aged 18-45 years; 2. Patients with chronic hepatitis B received nucleoside (acid) analogues for at least one year, and HBV DNA was below the detection limit; 3. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients during pregnancy or lactation; 2. Compensation or decompensation of hepatitis B cirrhosis; 3. Patients with viral hepatitis A, C, D, E and HIV infection; 4. Autoimmune liver disease, metabolic liver disease, alcoholic liver disease, malignant tumors, decompensated liver disease and organ transplantation patients; 5. Patients with severe neurological or psychiatric disorders; 6. Patients with severe hyperthyroidism and other autoimmune diseases; 7. Diabetic patients with poor blood sugar control; 8. Patients with retinal or fundus lesions; 9. Non-abstinent alcoholics/drug addicts; 10. Patients with severe heart disease, coronary heart disease and cerebrovascular disease; 11. Patients with poor epilepsy control; 12. Patients with contraindications in IFN instructions or Chinese guidelines for the treatment of chronic hepatitis C; 13. Researchers evaluated patients who were not suitable for admission.

Design outcomes

Primary

MeasureTime frame
HBsAg;

Contacts

Public ContactLu Xiaobo

First Affiliated Hospital of Xinjiang Medical University

zhengrongjiong@126.com+86 13999113773

Outcome results

None listed

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