CORSER: Sero-epidemiological Study of the SARS-CoV-2 Virus Responsible for COVID-19 in France

Sponsor
Institut Pasteur (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04325646
Collaborator
(none)
5,000
21
35.5
238.1
6.7

Study Details

Study Description

Brief Summary

On January 2020, the discovery of a new coronavirus (SARS-CoV-2) was officially announced by the Chinese health authorities and the World Health Organization (WHO). Its complete genome was sequenced by the laboratory of respiratory infection viruses at the Institut Pasteur on 29 January 2020 in France. This will allow the identification of antigenic structures involved in the immune response and the development of serological diagnostic tests.

Many questions are being asked about this new virus and the infection it causes, including questions about the percentage of asymptomatic and pauci-symptomatic forms. Serological studies can provide answers to these questions. There is no serological test for SARS-COV-2 yet, but the laboratory of respiratory infection viruses at the Institut Pasteur is working on its development.

This study proposes to carry out a collection of samples taken from subjects who travelled to China before the epidemic outbreak or suspected of being infected with SARS-CoV-2.

As soon as it is available, serology will be performed on the collected samples.

Condition or Disease Intervention/Treatment Phase
  • Other: Human Biological samples
  • Other: Human Biological samples

Detailed Description

On January 2020, the discovery of a new coronavirus (SARS-CoV-2) was officially announced by the Chinese health authorities and the World Health Organization (WHO). This new virus is presented as the causative agent of pneumonias. Its complete genome was sequenced by the laboratory of respiratory infection viruses at the Institut Pasteur on 29 January 2020 in France. This will allow the identification of antigenic structures involved in the immune response and the development of serological diagnostic tests.

Many questions are being asked about this new virus and the infection it causes, including questions about the transition from animal to human occur, the beginning of viral circulation in humans, the period of contagiousness, the percentage of asymptomatic and pauci-symptomatic forms. Serological studies can provide answers to these questions. There is no serological test for SARS-COV-2 yet, but the laboratory of respiratory infection viruses at the Institut Pasteur is working on its development.

This study proposes to carry out a collection of samples taken from subjects who travelled to China before the epidemic outbreak or suspected of being infected with SARS-CoV-2.

As soon as it is available, serology will be performed on the collected samples.

Study Design

Study Type:
Observational
Anticipated Enrollment :
5000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Sero-epidemiological Study of the SARS-CoV-2 Virus in France: Constitution of a Collection of Human Biological Samples
Actual Study Start Date :
Mar 13, 2020
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Feb 28, 2023

Arms and Interventions

Arm Intervention/Treatment
CORSER-1a

Subjects who had been to China in the weeks before the outbreak began

Other: Human Biological samples
Blood samples for serological tests

CORSER-1b

Subject who had a clinical profile compatible with an SARS-CoV-2 infection between August 1, 2019 and February 29, 2020

Other: Human Biological samples
Blood samples for serological tests

CORSER-2a

Subjects with suspected CoV-2-SARS infection with negative results from RT-PCR testing of respiratory specimens

Other: Human Biological samples
Blood samples for serological tests

CORSER-2b

Contacts or co-exposures of confirmed CoV-2-SARS infection cases, or who have worked or stayed in a hospital where confirmed CoV-2-SARS infection has been managed

Other: Human Biological samples
Blood samples for serological tests

CORSER-2c

Subjects who have been exposed to a risk of infection with SARS-CoV-2 in a geographical area of SARS-CoV-2 circulation. study among pupils, their parents and siblings, as well as teachers and non-teaching staff of a high-school located in Oise study among pupils from 5 to 12 and their parents in elementary schools located in Oise study among choir members

Other: Human Biological samples
Blood samples for serological tests

CORSER-2d

Staff of health care institutions

Other: Human Biological samples
Blood samples for serological tests

CORSER-2e

Subjects in care, hospitalized or residing in health care facilities

Other: Human Biological samples
Blood samples for serological tests

CORSER-3

Subjects returning from a humanitarian mission that started before 31/01/2020

Other: Human Biological samples
Blood samples for serological tests

CORSER-2f

Subjects with two symptomatic episodes of SARS-CoV-2 infection

Other: Human Biological samples
Blood samples, saliva, nasopharyngeal swab for serological tests

CORSER-4

Subjects being vaccinated against COVID-19

Other: Human Biological samples
Blood samples, saliva, nasopharyngeal swab for serological tests

CORSER-5

Subjects with acute SARS-CoV-2 infection and uninfected controls

Other: Human Biological samples
Blood samples, saliva, nasopharyngeal swab for serological tests

Outcome Measures

Primary Outcome Measures

  1. Presence of specific anti-SARS-CoV-2 antibodies in the different study groups. [One year]

    Description of the serological status of individuals by different detection tests

Secondary Outcome Measures

  1. Percentage of asymptomatic forms in individuals with anti-SARS-CoV-2 antibodies [One year]

    Proportion of asymptomatic subjects into seropositive population

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Affiliated with or benefiting from a Social Security system

  • State of health compatible with a blood sample as defined in the protocol

Exclusion Criteria:
  • Person benefiting from a legal protection measure or unable to express informed consent to participation

  • Have had an infectious episode and/or respiratory signs in the 14 days prior to the scheduled visit (CORSER 1 and 2a, 2b)

  • Have been in contact with a confirmed case of SARS-CoV-2 infection within 14 days prior to the date of the visit.(CORSER 1 and 2a, 2b)

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Amiens-Picardie Amiens France
2 EHPAD Villa Concorde Asnieres sur seine France
3 CHU François Mitterand Dijon France
4 Centre Hospitalier Départemental de Vendée La Roche-sur-Yon France
5 CHU Limoges Limoges France
6 Hôpital de la Croix Rousse Lyon France
7 EHPAD Les Etangs Mennecy France
8 CHRU de Nancy Nancy France
9 Hôpitaux de Brabois Nancy France
10 CHR Orléans Orléans France
11 Institut Mutualiste Paris France 75014
12 Centre Médical de l'Institut Pasteur Paris France 75015
13 Institut Pasteur Paris France 75015
14 EHPAD Villa Lecourbe Paris France
15 Hôpital la Pitié Salpetrière Paris France
16 CHU Poitiers Poitiers France
17 Hôpital Pontchaillou Rennes France
18 CHU Saint-Etienne Saint-Étienne France
19 CHRU de Strasbourg Strasbourg France
20 CH de Tourcoing Tourcoing France
21 Hôpital Bretonneau Tours France

Sponsors and Collaborators

  • Institut Pasteur

Investigators

  • Principal Investigator: Bruno HOEN, Pr, Institut Pasteur

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institut Pasteur
ClinicalTrials.gov Identifier:
NCT04325646
Other Study ID Numbers:
  • 2020-007
First Posted:
Mar 27, 2020
Last Update Posted:
Mar 23, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 23, 2022