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RT-PCR Database Analysis for COVID-19 Infections and Re-infection (ReCOV)

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ClinicalTrials.gov Identifier: NCT04653844
Recruitment Status : Recruiting
First Posted : December 4, 2020
Last Update Posted : January 4, 2022
Laboratoire CERBA-MPL
Nîmes University Hospital
Information provided by (Responsible Party):
University Hospital, Montpellier

Brief Summary:
The SARS-Cov2 pandemic remains associated with many concerns. One of the them is the real frequency of likely re-infection and subsequently the level of protection conferred by the acquired immunity following primary-infection. We propose to analyze a large set of laboratory data produced since the early beginning of the SARS-Cov2 spread in the French population to identify recurrent infection events and, more generally, gain insight about infection kinetics.

Condition or disease
Covid-19 SARS-CoV Infection

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Study Type : Observational
Estimated Enrollment : 7000000 participants
Observational Model: Other
Time Perspective: Retrospective
Official Title: SARS-Cov2 (COVID-19) Infection and Reinfection Through the Analysis of a RT-PCR Results Database
Actual Study Start Date : February 1, 2020
Estimated Primary Completion Date : December 31, 2022
Estimated Study Completion Date : January 30, 2023

Primary Outcome Measures :
  1. SARS-CoV-2 reinfection rate [ Time Frame: 1 day ]
    SARS-CoV-2 reinfection rate

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
French population with a positive SARS-Cov2 diagnosis documented through a positive RT-PCR result

Inclusion criteria:

- People with at least one positive SARS-Cov2 RT-PCR result with a known sampling date

Exclusion criteria:

- Patient refusing to participate in research

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04653844

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Contact: Samuel Alizon, PhD 610654902 ext 33 samuel.alizon@cnrs.fr
Contact: Vincent Foulongne, PhD 467 330 254 ext 33 v-foulongne@chu-montpellier.fr

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Uh Montpellier Recruiting
Montpellier, France, 34295
Contact: Vincent Foulongne, PHD    467 330 254 ext 33    v-foulongne@chu-montpellier.fr   
Sponsors and Collaborators
University Hospital, Montpellier
Laboratoire CERBA-MPL
Nîmes University Hospital
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Study Director: Vincent Foulongne, PhD UH MONTPELLIER
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Responsible Party: University Hospital, Montpellier
ClinicalTrials.gov Identifier: NCT04653844    
Other Study ID Numbers: RECHMPL20_0640
First Posted: December 4, 2020    Key Record Dates
Last Update Posted: January 4, 2022
Last Verified: January 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Plan Description: NC

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University Hospital, Montpellier:
SARS-Cov2 infection
Positive SARS-Cov2 RT-PCR
SARS-Cov2 immune status
Additional relevant MeSH terms:
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Communicable Diseases
Severe Acute Respiratory Syndrome
Disease Attributes
Pathologic Processes
Respiratory Tract Infections
Pneumonia, Viral
Virus Diseases
Coronavirus Infections
Coronaviridae Infections
Nidovirales Infections
RNA Virus Infections
Lung Diseases
Respiratory Tract Diseases