A Cohort of Patients With Possible or Confirmed SARS-CoV-2 (COVID-19)

NCT ID: NCT04347850

Last Updated: 2020-07-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-02-01

Study Completion Date

2022-12-30

Brief Summary

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SARV-CoV-2 infection was considered pandemic on March 11, 2020. The SARV-CoV-2 epidemic affected France from the beginning of March, spreading in particular from a 4-day large evangelical meeting of 2500 people on February 17 in the city of Mulhouse (North East of France). The Montpellier University Hospital has set up a clinical pathway for people suspected of being infected with SARV-CoV-2 because of signs compatible with pneumonia (screening criteria in France during the study period). This includes an emergency department, an infectious disease department dedicated to the surveillance of infected people requiring hospital treatment, and an intensive care unit for the most severe cases. The diagnosis of infection with SARV-CoV-2 was confirmed in approximately 20% of people initially referred in this special care system.

The main objective of this cohorte is the collection of clinical data and biological samples from care for non-interventional research on the patients with a possible or confirmed SARS-CoV -2 infection, from diagnosis to long-term follow-up.

Detailed Description

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Conditions

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SARS-CoV-2 COVID-19

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patient with Covid-19 confirmed (middle form)

Covid-19 confirmed: middle form

blood sample

Intervention Type OTHER

Collection

Patient with Covid-19 confirmed (severe form)

Covid-19 confirmed : severe form

blood sample

Intervention Type OTHER

Collection

Patient with Covid-19 not confirmed

Covid-19 not confirmed

blood sample

Intervention Type OTHER

Collection

Interventions

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blood sample

Collection

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

\- Patients care at the Montpellier University Hospital suspected of a COVID-19 infection

Exclusion Criteria

* Patient opposed to the use of his data for research purposes
* Patient deprived of liberty by judicial decision
* Patient not affiliated to a social security scheme
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Montpellier

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Edouard TUAILLON, MD; PhD

Role: STUDY_DIRECTOR

UH MONTPELLIER

Locations

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Uh Montpellier

Montpellier, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Edouard TUAILLON, MD; PhD

Role: CONTACT

467 338 469 ext. 33

Facility Contacts

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Edouard TUAILLON, MD; PhD

Role: primary

467 338 469 ext. 33

References

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Capelli N, Domitien Payet L, Alcocer Cordellat C, Pisoni A, Engelmann I, Van de Perre P, Jeziorski E, Tuaillon E. SARS-CoV-2 nucleocapsid antigen in plasma of children hospitalized for COVID-19 or with incidental detection of SARS-CoV-2 infection. J Med Virol. 2024 Jan;96(1):e29358. doi: 10.1002/jmv.29358.

Reference Type DERIVED
PMID: 38180230 (View on PubMed)

Other Identifiers

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RECHMPL20_0185

Identifier Type: -

Identifier Source: org_study_id

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