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Nucleos(t)ide analogue and alpha-interferon in combination long term for chronic hepatitis B: a clinical research

Nucleos(t)ide analogue and alpha-interferon in combination long term for chronic hepatitis B: a clinical research

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TNRC-10001067
Enrollment
Unknown
Registered
2010-10-19
Start date
2001-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Chronic hepatitis B

Interventions

nucleos(t)ide analogue monotherapy,taken once dail:nucleos(t)ide analogue monotherapy,taken once dail
Group B:alpha-interferon monotherapy,taken once week for 1year
Group C:nucleos(t)ide analogue combined with alpha-interferon,for 2 years

Sponsors

Beijing Youan Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 to 70 years old. 2.Consecutive adult patients with chronic hepatitis B were enrolled in the study. 3.Additional eligibility criteria were as follows: laboratory test results that were positive for both HBsAg and HBeAg for at least 6 months before the initiation of the study, HBV DNA>105copies/ml, alanine aminotransferase (ALT) levels>60 IU/L

Exclusion criteria

Exclusion criteria: Exclusion criteria included evidence of decompensated liver disease, co-infection with HAV, HCV, HDV and/or HIV, comorbidities or severe psychiatric disease, a neutrophil absolute count<1.0×109/L, a platelet count<5×109/L, a history of alcohol or drug abuse.

Design outcomes

Primary

MeasureTime frame
HBVDNA;HBeAg;HBsA;

Countries

China

Contacts

Public ContactXinyue Chen
chenxy63050639@yahoo.com.cn+86 13911212398

Outcome results

None listed

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