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临床试验/JPRN-UMIN000020312
JPRN-UMIN000020312已完成未知

Evaluation of clinical trial for the rapid detection kit of Respiratory Syncytial Virus - Evaluation of clinical trial for the rapid detection kit of RSV

Eiken Chemical Co.,Ltd.0 个研究点目标入组 400 人开始时间: 2015年12月22日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
400

研究概览

简要总结

For the nasal swab specimens, positive, negative and total concordance rates of RT-PCR with the rapid detection kit ware 89.9%(71/79), 100.0%(131/131), 96.2%(202/210), respectively. For the nasopharyngeal aspirates, positive, negative and total concordance rates of RT-PCR with the rapid detection kit ware 93.9%(46/49), 97.6%(83/85), 96.3%(129/134), respectively.

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients who have difficulty to collect Specimens 2) An investigator determines that a patient is unsuitable for this study

研究者

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