跳至主要内容
临床试验/JPRN-UMIN000041828
JPRN-UMIN000041828已完成未知

Clinical study to evaluate the Bordetella pertussis antigen kit for patients suspected to be infected with Bordetella pertussis - Clinical study to evaluate the Bordetella pertussis antigen kit for patients suspected to be infected with Bordetella pertussis

Asahi Kasei Pharma Corporation0 个研究点目标入组 203 人开始时间: 2020年10月1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
203

研究概览

简要总结

Sensitivity, specificity and total concordance rate of the antigen kit with real-time PCR were 86.4%, 97.1% and 95.9% respectively. Sensitivity, specificity and total concordance rate of the antigen kit with culture testing were 72.2%, 94.0% and 91.9% 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 refuse to collect nasopharyngeal swabs. 2. Patients who doctors judge to be inappropriate to participate in the study.

研究者

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