跳至主要内容
临床试验/NCT04367142
NCT04367142已完成不适用

Rapid Detection of COVID-19 by Portable and Connected Biosensor : Biological Proof of Concept

University Hospital, Lille1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2020年8月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200
试验地点
1
主要终点
Sensitivity and specificity of the COR-DIAL based on nasopharyngeal swabs taken on admission of the patient compared to the final diagnosis of COVID-19 made by the medical team

研究概览

简要总结

The objective of study is to estimate the sensitivity and specificity of the COR-DIAL based on nasopharyngeal samples taken at the patient's admission in relation to the final diagnosis of COVID-19 made by the medical team.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Male or female or child without age limit
  • Admitted to a Reference Health Establishment in an emergency unit, hospitalisation or intensive care unit for suspicion of SARS-CoV-2 infection, regardless of the clinical presentation and degree of severity.
  • Patient to be diagnosed using a PCR test on nasopharyngeal swab.
  • Social insured

排除标准

  • Atypical or suspicious cases without a final diagnosis of COVID-19 positive or negative
  • Patient refusal to participate

结局指标

主要结局

Sensitivity and specificity of the COR-DIAL based on nasopharyngeal swabs taken on admission of the patient compared to the final diagnosis of COVID-19 made by the medical team

时间窗: Baseline (at admission)

次要结局

  • Cohen's Kappa Coefficient for concordance for the diagnosis of CoV-2-SARS between PCR and COR-DIAL based on nasopharyngeal swabs taken on patient admission(Baseline (at admission))

研究者

发起方
University Hospital, Lille
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验