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临床试验/NCT04418206
NCT04418206已完成不适用

Validating an ELISpot for Early Detection of an Active Immune Response Against COVID-19

Centre Hospitalier Universitaire de Nice4 个研究点 分布在 1 个国家目标入组 950 人开始时间: 2020年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
950
试验地点
4
主要终点
IgA specific cells of SARS

研究概览

简要总结

The RT-PCR on rhino-pharynge sampling highlights the genetic material of the virus and indicates that a subject is infected with SARS-CoV-2. This test can be in about 30% of false negative cases, it does not allow to date the infection, nor to predict the asymptomatic, mild, moderate or severe evolution of the disease. In terms of public health, we need 1/ to better understand the chronology of the immune response to the virus in the general population and in contacts of index cases; 2/ To know which characteristics of the immune response are protective of future reinfections. Finally, in symptomatic subjects, we need biomarkers that predict the evolutionary mode of the disease (moderate vs. severe form).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age ≥ 18 years,
  • patients with confirmed SARS-Cov2 infection (RT PCR positive)
  • or patients suspected (evocative chest scanner)
  • OR patients exposure to SARS-CoV2 but no symptoms (patient's family, caregivers)
  • OR patients Non exposure to SARS-Cov2 volunteer subjects (general population)

排除标准

  • pregnant or breastfeeding female

结局指标

主要结局

IgA specific cells of SARS

时间窗: At 7 days

Proportion of subjects with IgA-specific cells of SARS-CoV-2's Spike 1 protein at inclusion and 7 +/-2 days later

次要结局

  • OMS progression scale(At 7 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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