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临床试验/jRCT1030240609
jRCT1030240609进行中(未招募)不适用

A Clinical Study To investigate Incidence Rate of Seasonal Influenza

Daiichi Sankyo Co., Ltd.0 个研究点目标入组 6,000 人开始时间: 2025年2月4日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
6,000

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

年龄范围
No limit 至 No limit(—)
性别
All

入选标准

  • Has provided written consent to research participation by the participant or via the legal representative.
  • Is not willing to receive a seasonal influenza vaccine after the date of consent until the end of research observation period.
  • Is able to visit the research institution upon report and undergo the tests specified in the protocol when seasonal influenza-like symptoms are observed during the research observation period (report by a legal representative is also acceptable).

排除标准

  • Is received a seasonal influenza vaccine from 6 months before the start of resarch observation period to the date of consent in each season.
  • Has a medical history of a seasonal influenza from 6 months before the start of resarch observation period to the date of consent in each season.

研究者

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