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临床试验/NCT03193775
NCT03193775已完成不适用

Impact of Hepatitis B Vaccination on HBsAg Kinetics, Interferon-inducible Protein 10 Level and Recurrence of Viremia

Zagazig University0 个研究点目标入组 220 人开始时间: 2011年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
220
主要终点
production of protective HBsAb

研究概览

简要总结

  • HBV is not curable with persistent HBsAg even after the disappearance of HBV DNA.
  • HBsAg > 1000 IU/ml is associated with the risk of virological recurrence and HCC.
  • There is an impaired immune response to HBsAg and HBV vaccine is an easily available, cost-effective, non-harmful method of stimulating immunity.

详细描述

Persistent HBs antigenemia >1000 IU/ml has a possibility of viral reactivation and hepatoma in 8%; the effect of HBV vaccine on HBsAg was investigated, recurrence of viremia, insulin resistance, and fibrosis regression.

From August 2011 to October 2016, 220 participants with chronic hepatitis B were evaluated at the hepatology clinic-Internal medicine department-Zagazig university-Egypt. They were enrolled after approval of the ethical committee of Zagazig university hospital. Written informed consent was obtained for the interview, clinical evaluation, and blood sampling.

participants were divided into two groups:

  • Inactive carriers (n=100) who were presented with persistent HBsAg, undetected HBV DNA, normal liver enzymes, positive HBeAb and had never been exposed to antiviral therapy.
  • Patients exposed to NAs (n=120): tenofovir 300mg (n=65) or Entecavir 1mg (n=55): A- HBeAg-positive patients (n=60) who received NAs until 1 year after HBe seroconversion and disappearance of HBV DNA with persistent HBsAg B- HBeAg-negative patients (n=60) who received NAs till 3 years after the disappearance of HBV DNA; all showed persistent HBsAg.
  • Exclusion criteria Clinically decompensated liver cirrhosis; hepatocellular carcinoma; other causes of liver disease or mixed causes (excessive alcohol consumption, autoimmune liver disease, immunosuppressive drugs, or who had been infected with hepatitis C virus.

B- Vaccination schedule

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

盲法说明

open label

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • HBV patients with persistent HBs antigenemia

排除标准

  • decompensated liver cirrhosis
  • hepatocellular carcinoma
  • other causes of liver disease or mixed causes (excessive alcohol consumption,
  • autoimmune liver disease
  • immunosuppressive drugs
  • infection with hepatitis C virus.

结局指标

主要结局

production of protective HBsAb

时间窗: three months after the last dose of vaccine

Current treatment by NAs may suppress HBV replication but cannot completely eradicate the virus due to the systemic immune tolerance or exhaustion. HBV vaccine may enhance the immunity against HBsAg and may be an efficient immunotherapy in chronic HBV.

次要结局

  • impact on Insulin resistance, fibrosis regression(3 month after the last dose of vaccination)

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Amr Shaaban Hanafy

Assistant professor

Zagazig University

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