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临床试验/ISRCTN30087513
ISRCTN30087513已完成不适用

A randomised comparative study of the immunogenicity of a modified intradermal post-exposure rabies vaccine regimen

niversity of Oxford (UK)0 个研究点目标入组 220 人开始时间: 2005年7月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
220

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Healthy volunteers in Oxfordshire between the ages of 18 and 50 years, either sex
  • 2. Have never had rabies vaccine before
  • 3. Able to attend all appointments

排除标准

  • 1. Any previous rabies immunisation
  • 2. Treatment with human immunoglobulins or blood transfusion within the past three months
  • 3. The use of immunosuppressive drugs
  • 4. Pregnancy
  • 5. Uncertainty about returning for appointments during the year
  • 6. Chloroquine cannot be taken for two weeks prior to vaccination at day zero until two weeks after vaccination at day 90

研究者

发起方
niversity of Oxford (UK)

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