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临床试验/NL-OMON21569
NL-OMON21569招募中不适用

Risk-group Infant Vaccination Agains RotavirusImplementation and Phase IV Effectiveness study

MC UtrechtHeidelberglaan 1003508 GA UtrechtThe Netherlands0 个研究点目标入组 2,000 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
2,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1. Infants 6 weeks 0 days to 13 weeks 6 days of age who receive medical care in hospital or through outpatient clinics at the time of the first vaccine dose administration in one of the participating hospitals and
  • 2. Diagnosed with at least one high-risk condition:

排除标准

  • Known hypersensitivity to any of the vaccine components.
  • Previous intussusception or an uncorrected congenital condition predisposing to intussusception (such as Meckel’s diverticle).

研究者

发起方
MC UtrechtHeidelberglaan 1003508 GA UtrechtThe Netherlands

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