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Antiviral treatment for chronic HBV infection in "uncertain period"

Antiviral treatment for chronic HBV infection in "uncertain period"

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103103
Enrollment
Unknown
Registered
2025-05-23
Start date
2024-08-17
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Chronic HBV infection in "indefinite period"

Interventions

Monotherapy with nucleos(t)ide analogues (NAs) for 52 weeks:None
Receiving peginterferon a-2b in combination with nucleos(t)ide analogues (NAs):None

Sponsors

Meishan City Peoples Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-60 years old; 2.HBsAg positive for more than 6 months. 3.ALT =20iu/mL; 5.Initial treatment (NAs or interferon anti-HBV drugs have not been used before).

Exclusion criteria

Exclusion criteria: 1.Patients with chronic hepatitis B; 2.Patients with ALT > 1× ULN; 3.Liver fibrosis, liver cirrhosis, liver cancer and other malignant tumors; 4.Alcoholics or drug addicts; 5.Patients with HAV, HCV, HDV and HEV infection and autoimmune liver disease; 6.Pregnant and lactating women,Those who need to use interferon should be excluded from family planning within 2 years. 7.The competent physician thinks that it is not suitable to participate in this research; 8.It is included in the interferon whole course/pulse combined treatment group; 9.(1) Contraindications to interferon (2)autoimmune diseases, psychosis (depression, etc.), diabetes and abnormal thyroid function(3) serious basic diseases: cardiovascular diseases, lung diseases, kidney diseases, brain and fundus diseases (4)low leukocyte/leukocyte ratio in peripheral blood: < 2×10^9/L and/or platelet count < 100× 100.

Design outcomes

Primary

MeasureTime frame
HBV DNA;HBsAg;HBeAg;

Secondary

MeasureTime frame
HBeAg seroconversion;The decrease/proportion of HBV-DNA, HBeAg, and HBsAg compared to baseline at the end of treatment;HBsAg seroconversion;

Countries

China

Contacts

Public ContactLiu Jiahao

Meishan City Peoples Hospital

844043406@qq.com+86 18783953817

Outcome results

None listed

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