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临床试验/ISRCTN57452882
ISRCTN57452882已完成不适用

A double-blind randomised placebo controlled dose escalating phase Ib/IIa study to evaluate the safety and immunogenicity of live attenuated rotavirus vaccine 116E in healthy non-malnourished infants eight to 20 weeks of age

Bharat Biotech International Ltd (India)0 个研究点目标入组 540 人开始时间: 2006年7月26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
540

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. Access to a telephone
  • 2. Healthy male and female non-malnourished infants aged six weeks (till six weeks + two days)
  • 3. Parents' permission to participate
  • 4. No plans to travel over the next four months

排除标准

  • 1. Gestational age less than 37 weeks
  • 2. Any major physical congenital malformation
  • 3. Contact with immunosuppressed individuals
  • 4. Hospitalised once or more for the following illnesses since birth: heart disease, pneumonia, sepsis, meningitis, unconsciousness
  • 5. Daily medications other than vitamins or herbal tonics
  • 6. Evidence of cardiovascular disease
  • 7. Evidence of gastrointestinal disease
  • 9. Evidence of liver or reticuloendothelial disease
  • 10. Evidence of hematologic, rheumatologic or immunologic disease
  • 11. Evidence of renal disease

研究者

发起方
Bharat Biotech International Ltd (India)

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