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Reversal of innate and adaptive lymphocytes hyperactivation and functional impairment is associated with HBsAg seroconversion in HBeAg negative chronic hepatitis B patients upon interferon and nucleos(t)ide-analogue combination therapy

Reversal of innate and adaptive lymphocytes hyperactivation and functional impairment is associated with HBsAg seroconversion in HBeAg negative chronic hepatitis B patients upon interferon and nucleos(t)ide-analogue combination therapy

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024737
Enrollment
Unknown
Registered
2019-07-25
Start date
2019-07-17
Completion date
Unknown
Last updated
2019-07-29

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

Conditions

Chronic hepatitis B

Interventions

1:IFN and NUC
2:NUC

Sponsors

Beijing You'an Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 72 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The criteria for diagnosis of HBeAg-negative CHB in China's Guidelines for the Prevention and Treatment of Chronic Hepatitis B (2015 edition) were in line with the following points: (1) aged 18-60 years, gender-unlimited; (2) treatment with pegylated interferon combined with sequential nucleotide analogues for at least 96 weeks.

Exclusion criteria

Exclusion criteria: (1) patients with HAV, HCV, HDV, HEV infection and autoimmune liver disease; (2) pregnant women, lactating women and patients who are about to give birth in the near future; (3) severe liver dysfunction or decompensated cirrhosis; (4) a history of severe heart disease, including unstable or uncontrolled heart disease within 6 months; (5) a history istory of mental illness or mental illness. (6) there is uncontrollable epilepsy. (7) unabstained alcoholics or drug addicts. (8) uncontrolled diabetes mellitus, hypertension, thyroid diseases, retinopathy, autoimmune diseases, etc. (9) neutrophil count < 110 *10 ^9/L and/or platelet count < 50 *10 ^9/L before treatment. (10) total bilirubin 51 umol/L (especially indirect bilirubin).

Design outcomes

Primary

MeasureTime frame
Immunological changes;

Countries

China

Contacts

Public ContactRen Shan

Beijing You,an Hospital, Capital Medical University

13811361553@163.com+86 13811361553

Outcome results

None listed

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