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临床试验/NCT04448769
NCT04448769已完成不适用

Epidemiological Study of Seroprevalence Against the SARS-CoV-2 Virus (COVID-19) in the Population of the Grand Nancy Metropolitan Area

Central Hospital, Nancy, France2 个研究点 分布在 1 个国家目标入组 2,006 人开始时间: 2020年6月26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
2,006
试验地点
2
主要终点
Anti-SARS-CoV-2 IgT (IgM/IgA/IgG) seropositivity

研究概览

简要总结

In order to inform the public decision on the containment strategy and knowledge of the intensity of the epidemic during post-containment, estimates of the share of the population infected with the SARS-CoV-2 virus responsible for COVID-19 disease at the territorial level are needed as soon as possible. The aim of the study is to estimate the prevalence of positive anti-SARS-CoV-2 serologies by detection of IgT-total antibodies (IgM/IgA/IgG) in the general population of the Grand Nancy Metropolitan area.

A study of seroprevalence and symptom collection, or absence of symptoms, on a cluster (household) sample of the Grand Nancy Metropolitan population randomly selected will be conducted.

The target population consists of all the inhabitants of the Grand Nancy Metropolitan area, from which a sample is drawn from the electoral lists (households) in a random manner to ensure representativeness. In order to ultimately include 2000 people in the study

详细描述

In order to inform the public decision on the containment strategy and knowledge of the intensity of the epidemic during post-containment, estimates of the share of the population infected with the SARS-CoV-2 virus responsible for COVID-19 disease at the territorial level are needed as soon as possible. To date, these estimates are based on RT-qPCR tests carried out on individuals with symptoms of the disease, on people likely to present severe forms of COVID-19, known as 'vulnerable', or on the number of hospitalizations/deaths related to COVID-19. In order to refine these estimates, it is crucial to carry out measurements on a random sample of the population and to take biological samples for serological testing, in accordance with the recommendations of the HAS and the scientific societies.

Besides, it is important to assess the proportion of persons reporting that they have not developed symptoms of COVID-19 since the beginning of the epidemic among seropositive persons.

The aim of the study is to estimate the prevalence of positive anti-SARS-CoV-2 serologies by detection of IgT-total antibodies (IgM/IgA/IgG) in the general population of the Grand Nancy Metropolitan area.

A study of seroprevalence and symptom collection, or absence of symptoms, on a cluster (household) sample of the GNM population randomly selected.

It is a cross-sectional, not experimental study in the sense that it does not alter the exposure of participants; however, it does require a blood sample, which classifies it as minimal risk intervention research according to French law. The study is monocentric.

研究设计

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

入排标准

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

入选标准

  • Person who has received full information about the research organization and signed informed consent
  • Person residing in the Grand Nancy Metropolitan area
  • Person aged at least 5 years on 1 June 2020 and weighing more than 7 kg

排除标准

  • Children under 5 years of age at the time of collection
  • Person referred to in Articles L1121-8 of the Public Health Code. A person of full age who is subject to a legal protection measure (guardianship, curatorship, legal protection).
  • Adult person unable to give consent
  • Persons deprived of their liberty by a judicial or administrative decision, persons under psychiatric care pursuant to articles L. 3212-1 and L. 3213-1.

结局指标

主要结局

Anti-SARS-CoV-2 IgT (IgM/IgA/IgG) seropositivity

时间窗: through study completion, an average of 4 hours

Anti-SARS-CoV-2 IgT seropositivity of the individuals tested in the population of the Grand Nancy Metropolitan area

次要结局

  • Proportion of asymptomatic, symptomatic cases among seropositive people(through study completion, an average of 4 hours)
  • Proportion of infected households(through study completion, an average of 4 hours)
  • Anti-SARS-CoV-2 IgT seropositivity in the household(through study completion, an average of 4 hours)
  • Proportion of asymptomatic cases among seropositive people(through study completion, an average of 4 hours)
  • Identification of risk groups - Anti-SARS-CoV-2 IgT seropositivity by age, sex and as a function of weight status, smoking status, work activity and social status.(through study completion, an average of 4 hours)
  • Proportion of seropositive subjects according to the level of social disadvantage measured by the EPICES score(through study completion, an average of 4 hours)
  • Clinical expression patterns of infection by symptom/antibody association(through study completion, an average of 4 hours)
  • Serological Response to Infection(through study completion, an average of 4 hours)
  • Anti-SARS-CoV-2 IgT seropositivity(through study completion, an average of 4 hours)
  • • Evaluation of serum neutralisation of persons positive for anti-SARS-CoV-2 antibodies, of the infectivity of viral strains in cell culture: percentage neutralisation compared to a viral strain not exposed to seropositive serum.(through study completion, an average of 4 hours)

研究者

发起方
Central Hospital, Nancy, France
申办方类型
Other
责任方
Principal Investigator
主要研究者

Evelyne Schvoerer

Pr

Central Hospital, Nancy, France

研究点 (2)

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