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临床试验/NCT02959775
NCT02959775已完成4 期

Immunogenicity and Safety of High-dose Hepatitis B Vaccine Among Drug Users: a Randomized, Controlled Trial

Shanxi Medical University0 个研究点目标入组 480 人开始时间: 2014年8月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
480
主要终点
Number and Rate of Participants With Anti-HBs Seroconversion at Month 7

研究概览

简要总结

Uptake, adherence, and completion of vaccination among drug users were low, and their immune function and immune response to hepatitis B vaccination were also suboptimal, indicating that the current practice of hepatitis B vaccination can't protect drug users from HBV infection.

This is a randomized, open-label, blank-controlled trial, conducted among drug users with drug rehabilitation. This study will compare the immunogenicity and safety of three intramuscular 20µg and 60µg recombinant hepatitis B vaccines at months 0, 1, and 6 among drug users

详细描述

Comparison of 2 vaccination strategy against Hepatitis B in Drug Users

Intervention:

Arm 1 : Receive three intramuscular injections of 60 µg recombinant hepatitis B vaccine at months 0, 1 and 6;

Arm 2 : Receive three intramuscular injections of 20 µg recombinant hepatitis B vaccine at months 0, 1 and 6;

Arm 3 : Receive no vaccination during the study period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Aged between 18 and 70 years at the enrolment
  • current illicit drug users before drug rehabilitation
  • negative for hepatitis B surface antigen (HBsAg) and hepatitis B surface antibody (anti-HBs) at enrollment
  • having spent acute physiological detoxification phase

排除标准

  • any intolerance or allergy to any component of the vaccine
  • ongoing opportunistic infection
  • liver disease
  • hemopathy
  • unexplained fever in the last week before the recruiting

结局指标

主要结局

Number and Rate of Participants With Anti-HBs Seroconversion at Month 7

时间窗: Month 7

The measurements of anti-HBs antibodies were determined quantitatively by CMIA(Chemiluminescent Microparticle Immunoassay). The accepted protective serum anti-HBs level was ≥10 mIU/ml.

次要结局

  • Number and Rate of Participants With Anti-HBs Seroconversion at Month 12(Month 12)
  • Anti-HBs Concentration at Month 7(Month 7)
  • Occurrence of Adverse Events After Vaccination(Within 28 days after the vaccination, at Month 0, 1, and 6)
  • Anti-HBs Concentration at Month 12(Month 12)
  • Serious Adverse Events (SAE) Occurred During Month 12(Month 0-12)

研究者

发起方
Shanxi Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Suping Wang

Professor

Shanxi Medical University

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