ACTRN12609000905268尚未招募2 期
Immunogenicity and safety of acellular pertussis vaccine given at birth in healthy infants
Peter McIntyre0 个研究点目标入组 400 人开始时间: 2009年10月19日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 1 Hours 至 5 Days（—）
- 性别
- All
入选标准
- •Healthy infants (by history and physical examination) at the time of first vaccine, born at 37 weeks gestation or greater whose parents give written informed consent.
排除标准
- •1.Contraindications to vaccination as listed in the Immunisation Handbook 9th Edition
- •2.Infant of mother known to be a carrier of hepatitis B virus
- •3.Administration of immunoglobulins and any blood products preceding the first dose of study vaccine or planned administration during the study period.
- •4.Any confirmed or suspected immunosuppressive or immunodeficient condition, in parent or child
- •5.Major congenital defects or serious chronic illness
研究者
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