[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100390832":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":24,"centralContacts":10,"locations":28,"responsibleParty":46,"collaborators":10,"id":48,"slug":49,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":10,"enrollmentInfo":59,"targetDuration":10,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":68,"overallStatus":71,"whyStopped":10,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Institut Curie","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"Subjects who are not showing active SARS-Cov2 infection",null,[12,13],"Diagnostic Test: Blood samples (collection of 5 mL of blood in a dry tube)","Diagnostic Test: Nasopharyngeal swabs",[15,20],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"DIAGNOSTIC_TEST","Blood samples (collection of 5 mL of blood in a dry tube)","A nurse will take blood samples under safe conditions compatible with the pandemic period and while respecting the protection of the volunteer's personal data.\n\nThe blood samples will be taken at 4 times for Institute Curie and Institute Pasteur: T0, between 6 weeks and 3 months ,6 months and 12 months post-inclusion.\n\nFor volunteers already included at Institute Curie : in case of proved (RT-PCR+ or antigenic +) or very likely (anosmia and\u002For ageusia, and\u002For digestive syndrome with associated respiratory signs) between 2 sampling times already planned in the flow chart, blood samples shall be performed, if time since last planned sampling(s) has been more than 3 weeks or if time until next sampling(s) is more than 3 weeks.\n\nThe serum samples will be extracted and collected prospectively from the blood samples.\n\nFor each blood sample, a sample number will be assigned by the laboratory management system of the Department of Biology at Institut Curie.",[9],{"type":16,"name":21,"description":22,"armGroupLabels":23,"otherNames":10},"Nasopharyngeal swabs","The nasopharyngeal swabs will be performed between 6 weeks and 3 months, 6 months and 12 months post-inclusion for Institute Curie staff with at least one of the following criteria: have had RT-PCR+, and\u002For presence of antibodies at the 95% threshold, and\u002For anosmia\u002Fageusia, and\u002For digestive syndrome with associated respiratory signs.\n\nThe nasopharyngeal swab shall also be proposed to volunteers not meeting the above listed criteria to have a control group (about 100 volunteers).\n\nFor volunteers already included at Institute Curie : in case of proved (RT-PCR+ or antigenic +) or very likely (anosmia and\u002For ageusia, and\u002For digestive syndrome with associated respiratory signs) infection between 2 sampling times, nasopharyngeal swabs shall be performed if time since last planned sampling(s) has been more than 3 weeks or if time until next sampling(s) is more than 3 weeks.\n\nThe nasopharyngeal swabs will be performed at T0 for Institute Pasteur staff so 4 times in total.",[9],[25],{"name":26,"affiliation":5,"role":27},"Pierre Fumoleau, PhD","STUDY_DIRECTOR",[29,40],{"facility":5,"status":10,"city":30,"state":10,"zip":31,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":10},"Paris","75005","France","FR",{"type":35,"coordinates":36},"Point",[37,38],2.3488,48.85341,{"lat":38,"lon":37},{"facility":41,"status":10,"city":30,"state":10,"zip":42,"country":32,"countryCode":33,"cosmosGeoPoint":43,"geoPoint":45,"contacts":10},"Institut Pasteur","75015",{"type":35,"coordinates":44},[37,38],{"lat":38,"lon":37},{"type":47,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100390832","covid-19-study-of-the-serological-response-against-the-severe-acute-respiratory-syndrome-sars-coronavirus-2-cov-2-virus-in-2-types-of-employees-hospital-and-non-hospital-at-institute-curie-and-institute-pasteur-100390832",false,"NCT04369066","COVID-19 Study of the Serological Response Against the Severe Acute Respiratory Syndrome (SARS) Coronavirus 2 (CoV-2) Virus in 2 Types of Employees, Hospital and Non-hospital, at Institute Curie and Institute Pasteur","COVID-19 Study of the Serological Response Against the SARS-CoV-2 Virus in 2 Types of Employees, Hospital and Non-hospital, at Institute Curie and Institute Pasteur","Curie-O-SA","Inclusion Criteria:\n\n1. Person, adult volunteer outside of any acute infectious episode with SARS-CoV-2\\* (see paragraph indication), working at the Institute Curie and able to exercise their professional activity on one of the 3 sites of the Institute Curie: Paris, Orsay or Saint Cloud, or on the Campus of the Institute Pasteur.\n2. Person aged 18 or over.\n3. Information and consent of the person to the procedures related to the study (cf. information note \u002F consent).\n\nFrom November 2020, person having presented at least one of the following criteria since January 2020:\n\n* A positive diagnostic test for SARS-COV-2 by PCR on a nasopharyngeal sample or antigenic test,\n* A positive SARS-CoV-2 serology,\n* An anosmia or \u002F and an ageusia,\n* A respiratory infection \\*\\* associated with digestive signs \\*\\*\n\nwhatever the working methods during confinement \\* Subjects who are not showing active SARS-CoV-2 infection are considered volunteers at the time of inclusion: people with no clinical signs \\*\\* suggestive of SARS-CoV-2 infection at the time of collection or having had an end of symptoms for more than 7 days \\[1\\].\n\n\\*\\* fever, fatigue, cough, shortness of breath, difficulty to breath, loss of taste or smell, headache, body aches, conjunctivitis or cold, digestive problems (vomiting, diarrhea), whether or not the signs led to sick leave, treatment and \u002F or hospitalization \\[2\\].\n\nExclusion Criteria:\n\n* Declaration by the subject of signs suggestive of Coronavirus Infectious Disease 2019 (COVID-19) infection with SARS-CoV-2 in progress or for which the end of symptoms dates from less than 7 days\n* Inability to submit to study monitoring for geographic, social or psychological reasons",true,"ALL","18 Years",{"count":60,"type":61},1971,"ACTUAL","INTERVENTIONAL",[64],"NA","This research proposes to study a large healthy population active for the presence of antibodies directed against the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) virus and this over time.\n\nAfter verification of the inclusion criteria and information by the coordinating investigative doctor, the volunteers sign a written consent. A nurse will take blood samples under safe conditions compatible with the pandemic period and while respecting the protection of the volunteer's personal data.\n\nThe blood samples will be taken at 4 times for Institute Curie and Institute Pasteur: T0 (day of inclusion), between 6 weeks and 3 months ,6 months and 12 months post-inclusion.\n\nEach blood sample consists of a collection of 5 mL of blood in a dry tube. The serum samples will be extracted and collected prospectively from the blood samples.\n\nThe nasopharyngeal swabs will be performed at 3 times: , between 6 weeks and 3 months, 6 months and 12 months post-inclusion for Institute Curie staff who have had at least one of the following four criteria on the sample or questionnaire carried out at T0:\n\n* have had RT-PCR+\n* and\u002For presence of antibodies at the 95% threshold\n* and\u002For anosmia\u002Fageusia\n* and\u002For digestive syndrome with associated respiratory signs. In case of infection between sampling times, if the volunteer meets one of the four criteria above, a nasopharyngeal swab will be performed during the following visits.\n\nThe nasopharyngeal swab shall also be proposed to volunteers not meeting the 4 above listed criteria in order to have a control group (about 100 volunteers) for future statistical analyses.\n\nIf the volunteers accept, naso-pharyngeal swab shall be performed between 6 weeks and 3 months, 6 months and 12 months after inclusion.\n\nFor volunteers already included at Institute Curie : in case of proved (RT-PCR+ or antigenic +) or very likely (anosmia and\u002For ageusia, and\u002For digestive syndrome with associated respiratory signs) between 2 sampling times already planned in the flow chart, blood samples and nasopharyngeal swabs shall be performed.\n\nThose shall be performed if time since last planned sampling(s) has been more than 3 weeks or if time until next sampling(s) is more than 3 weeks.\n\nThe blood samplings and nasopharyngeal swabs will be performed at 4 times for Institute Pasteur personnel: at T0 (inclusion day), between 6 weeks and 3 months, at 6 months and 12 months post-inclusion",[67],"Volunteers From the Institute Curie and Institute Pasteur Staff Who Are Not Showing Active SARS-CoV-2 Infection",[69,70],"Adults","Volunteers","COMPLETED","2025-09-18",{"date":74,"type":61},"2025-09-23",{"date":76,"type":61},"2020-04-28",{"date":78,"type":61},"2022-05-13",{"name":5,"class":6},2]