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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04653844
Recruitment Status : Active, not recruiting
First Posted : December 4, 2020
Last Update Posted : December 7, 2020
Sponsor:
Collaborators:
Laboratoire CERBA-MPL
CNRS (MIVEGEC)
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
Actual 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 : February 20, 2021
Estimated Study Completion Date : March 30, 2021

Resource links provided by the National Library of Medicine





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
Criteria

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


Locations
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France
Uh Montpellier
Montpellier, France, 34295
Sponsors and Collaborators
University Hospital, Montpellier
Laboratoire CERBA-MPL
CNRS (MIVEGEC)
Nîmes University Hospital
Investigators
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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: December 7, 2020
Last Verified: December 2020
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
reinfection
kinetics
Rt-PCR
immunity
Additional relevant MeSH terms:
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Infection
Communicable Diseases
Coronavirus Infections
Severe Acute Respiratory Syndrome
Coronaviridae Infections
Nidovirales Infections
RNA Virus Infections
Virus Diseases
Respiratory Tract Infections
Respiratory Tract Diseases