Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04481529
Other study ID # 87RI20_0049/SEROCO
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 29, 2020
Est. completion date January 15, 2021

Study information

Verified date November 2020
Source University Hospital, Limoges
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hospital staff, on the front line in the COVID-19 crisis, have many questions about the risk that they have been infected with this potentially fatal virus. These questions of course primarily concern caregivers working in sectors dedicated to COVID-19 patients, whether they are resuscitating or not, but also those in non-COVID-19 sectors, or even staff without direct contact with patients. In addition, depending on the suddenness and intensity of this "COVID-19 wave", these personnel have been more or less trained and sometimes exposed due to the dire lack of protective equipment. In some countries such as Great Britain, this has resulted in significant absenteeism, a source of deepening the shortage of caregivers. This proportion of contaminated caregivers has not been evaluated on the whole of French territory. Studies from other countries suggest figures ranging from 1.5% in China to 20% in Italy. It is therefore impossible to rely on such variable data to have a reliable estimate. Since june 2020, all staff in French health establishments could benefit a serological test. Thus, in this epidemiological study, we propose to rely on this institutional serological screening to describe the link between seroconversion of hospital staff, regional intensity of the epidemic, and sectors of activity (COVID-19 sectors, non-COVID-19 caregivers , non-COVID-19 non-caregivers.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1576
Est. completion date January 15, 2021
Est. primary completion date December 15, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Hospital staff from Argenteuil, Belfort, Dijon and Limoges hospitals. - Age = 18 years old - Participation agreement Exclusion Criteria: - Protected persons - Refusal of participation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Health Questionnaire
Completion of a short questionnaire noting the result of the serology and looking for elements in favor of exposure to the virus, whether professional or extra-professional.

Locations

Country Name City State
France CH Argenteuil - Service de Réanimation Argenteuil
France Ch Belfort Belfort
France CHU Dijon - Serve de Réanimation Dijon
France CHU de Limoges Limoges

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Limoges

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of subjects with a COVID-19 seroconversion Number of subjects with a COVID-19 seroconversion fixed by the presence of IgG + in serology according to the service (COVID19 +, COVID19- caregiver, COVID- non-caregiver). through study completion, an average of 5 month
See also
  Status Clinical Trial Phase
Recruiting NCT06178822 - Towards Novel BIOmarkers to Diagnose SEPsis on the Emergency Room
Completed NCT04239521 - The Epidemiology, Management, and the Associated Burden of Related Conditions in Alopecia Areata
Completed NCT05041764 - RNA Sequencing of Individual Versus Wastewater - SARS-CoV2
Recruiting NCT03818334 - Post Transplant Cyclophosphamide in Matched Unrelated Donor Stem Cell Transplantation for Hematological Malignancies Phase 2/Phase 3
Completed NCT04637867 - COVID-19 - Multicentre Study on Nosocomial Transmission of SARS-CoV-2 Virus: an Ancillary Study (NOSO-COR IMMUNO) N/A
Recruiting NCT06149494 - RCT of Vapendavir in Patients With COPD and Human Rhinovirus/Enterovirus Upper Respiratory Infection Phase 2
Completed NCT05069623 - A Phase 1/2 Study to Determine Safety and Immunogenicity of Two COVID 19 Vaccines VB10.2129 (RBD Candidate) and VB10.2210 (T Cell Candidate) Previously Vaccinated in Healthy Adult Volunteers Phase 1/Phase 2
Recruiting NCT04386460 - Covid-19 and Prevention of Malnutrition After Confinement by Dentists
Completed NCT04290780 - COVID-19 - Multicenter Study on Nosocomial Transmission of SARS-CoV-2 Virus
Completed NCT04327180 - PREdiction of DIagnosed Covid-19 infecTion in IUC Patients
Recruiting NCT04438629 - Evaluation of Immune Response in COVID-19 Patients
Active, not recruiting NCT05874713 - Study to Evaluate Safety and Immunogenicity of Different Priming and Booster Regimens With Adjuvanted H5N8 and/or H5N6 Influenza Vaccine in Adults Phase 2
Completed NCT03163628 - biomArkers to differeNtiate bacTerial From vIral iNfEctions N/A
Completed NCT04924842 - COVID-19 - SARS-CoV-2 Community Contamination in Children and Adults - Impact of Variants (Dyn3CEA - Nosocor Phase 2)
Completed NCT04354155 - COVID-19 Anticoagulation in Children - Thromboprophlaxis (COVAC-TP) Trial Phase 2
Recruiting NCT05875961 - Study to Evaluate Immunogenicity, Safety and Tolerability of Adjuvanted and Non-Adjuvanted H2N3 Influenza Vaccines in Adults Phase 1
Recruiting NCT06379061 - Access MeMed BV Assay Clinical Study Collection Protocol - Infectious Adult and Pediatric Cohorts
Recruiting NCT05090319 - Micro-hematology Analyzer for Viral/Bacterial Description
Not yet recruiting NCT04887233 - Efficacy and Safety of Longan Extract Spray (P80 Spray) in Volunteers With Coronavirus Disease 2019 (COVID-19) N/A
Completed NCT04754633 - Comparison of Chest CT Findings Related to COVID-19 With RSNA and BSTI Guidelines