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临床试验/NCT01017172
NCT01017172Unknown4 期

Safety and Immune Response to Adjuvanted A(H1N1)v Influenza Vaccine in HIV-1 Infected and Immunosuppressed Adults

Goethe University2 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2009年11月1日最近更新:
适应症

试验速览

阶段
4 期
发起方
入组人数
500
试验地点
2
主要终点
To investigate the immunogenicity via anti-hemagglutinin responses following an adjuvanted H1N1 vaccination in HIV-positive and immunosuppressed adult patients

研究概览

简要总结

The purpose of this study is to evaluate the immunogenicity and safety of an adjuvanted A(H1N1)v influenza vaccine in HIV-infected and immunosuppressed patients after one and two injections.

详细描述

The efficacy of an adjuvanted A(H1N1)v influenza vaccine in HIV-infected and immunosuppressed patients is unknown. Therefore we aim to investigate the immunoresponse as assessed by a anti-hemagglutinin assay before, 21 days after the first and 21 days after the second vaccination. The safety of the vaccination will be recorded by a standardized questionaire.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • written informed consent
  • HIV-1 infection
  • immunosuppressive treatment

排除标准

  • not willing to participate

结局指标

主要结局

To investigate the immunogenicity via anti-hemagglutinin responses following an adjuvanted H1N1 vaccination in HIV-positive and immunosuppressed adult patients

时间窗: baseline, day 21, day 42

次要结局

  • To evaluate the effect of pre-existing anti-influenza immunity and recent history of seasonal influenza and H5N1 vaccination on seroresponses to the H1N1 influenza vaccine(baseline)
  • To evaluate potential adverse reactions of the H1N1 vaccine(baseline, day 21, day 42)

研究者

发起方
Goethe University
申办方类型
Other

研究点 (2)

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