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Prospective and effective randomized controlled clinical study of pegylated interferon in the treatment of inactive HBV carriers

Prospective and effective randomized controlled clinical study of pegylated interferon in the treatment of inactive HBV carriers

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032748
Enrollment
Unknown
Registered
2020-05-09
Start date
2019-06-19
Completion date
Unknown
Last updated
2020-05-11

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

Conditions

inactive HBV infectio

Interventions

Experimental group:Peg IFN alpha 180ug/kg once every week for 48 weeks
control group:No treatment

Sponsors

The Fifth Medical Center of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. HBsAg positive > 6 months, and HBsAg 40g/LINR 0.8-1.2; 6. WBC (4-10)x10^9/LPLT(100-300)x10^9/L; 7. LSM < 6.4kpa or G < 2, s < 2; 8. There was no antiviral treatment in the past year; 9. Aged 18-60 years; 10. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Other liver diseases (including HCV / HDV / HIV infection, autoimmune liver disease, metabolic liver disease, alcoholic liver disease, cirrhosis, liver or other system tumors, etc.); 2. It is not suitable for interferon treatment (including but not limited to autoimmune diseases, thyroid dysfunction, emotional disorders, having fertility requirements in recent two years, etc.); 3. Other events that the researchers believe should be excluded.

Design outcomes

Primary

MeasureTime frame
the clearence of HBsAg;

Secondary

MeasureTime frame
HBV DNA;the quantitation of HBsAg;

Countries

China

Contacts

Public ContactSa Lv

The Fifth Medical Center of PLA General Hospital

lvsa@sina.com+86 13436664966

Outcome results

None listed

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