Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06803368

Research on Clinical Recovery and Maintenance Strategies for CHB

Led by Beijing Municipal Administration of Hospitals · Updated on 2025-01-31

285

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Collect basic information of patients before antiviral treatment and when HBsAg disappears, and divide them into three groups A, B, and C based on baseline anti HBs titers after informed consent. During the follow-up period of all patients, clinical biochemistry, virology (HBVDNA, HBVRNA), serological indicators (HBsAg, anti HBs, HBeAg, anti HBe, HBcrAg, anti HBc), AFP, Fibroscan, liver imaging examinations will be conducted every 3-6 months, and blood samples will be retained for monitoring the frequency of immune cells (pDC, Treg) and the expression of functional molecules, as well as cytokines (IFN - γ, IP-10, IL-10, and TGF - β). Observe the sustained response rate and recurrence rate of virological and serological indicators, as well as the incidence of hepatitis and liver cancer during the follow-up period.

CONDITIONS

Official Title

Research on Clinical Recovery and Maintenance Strategies for CHB

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years old
  • Gender is not limited
  • Diagnosis of chronic hepatitis B according to 2019 guidelines
  • Confirmed interferon treatment resulting in disappearance of HBsAg, negative HBeAg, and HBV DNA below detection limit
  • Written informed consent signed
Not Eligible

You will not qualify if you...

  • Co-infection with hepatitis C virus, hepatitis D virus, or HIV
  • Autoimmune liver disease
  • Long-term alcohol abuse or use of other liver-damaging drugs
  • Mental illness
  • Evidence of liver tumors or AFP greater than 100 ng/ml
  • Decompensated cirrhosis
  • Serious diseases of heart, brain, lungs, kidneys, or other systems preventing long-term follow-up

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beijing Ditan Hospital

Beijing, Beijing Municipality, China, 100015

Actively Recruiting

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Research Team

L

Lu Zhang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

3

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