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This page gives you access to all the studies carried out by French researchers, identified on Covid-19.

To view other resources related to Covid-19, click here.


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Métadonnées
Identification
General Aspects
Scientific investigator(s) (Contact)
Collaborations
Funding
Governance of the database
Additional contact
Type of database
Database objective
Population type
Dates
Size of the database
Data
Procedures
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Covid-19 : 84 forms

Sorting of results :

HOME-CoV - Hospitalization or Outpatient ManagEment of patients with a proven or probable SARS-CoV-2 infection

Head : DOUILLET Delphine

Version 1
Overview

25

Last update : 02/03/2021

HOME-CoV - Hospitalization or Outpatient ManagEment of patients with a proven or probable SARS-CoV-2 infection

Head : DOUILLET Delphine

Main objective

the composite rate of adverse outcomes [ Time Frame: day 7 ]
Adverse outcomes include intubation with mechanical ventilation requirement and death (Stage ≥ 6 on "Ordinal Scale for Clinical Improvement" of the World Health Organization) within 7 days after inclusion.

Inclusion criteria

The rate of hospitalization [ Time Frame: 24 hours ]
The rate of patients hospitalized after admission to the emergency room including patients discharged home more than 24 hours after admission.

It will be analyzed in a hierarchical approach, only if first primary objective is positive i.e. non-inferiority of HOME-CoV strategy versus current practice on the rate of adverse outcomes.

LICORNE - Predictive factors for mortality at D28 for patients managed at Lille University Hospital for COVID-19

Head : CHOPIN Marie Charlotte
DEPLANQUE Dominique

Version 1
Overview

26

Last update : 05/05/2021

LICORNE - Predictive factors for mortality at D28 for patients managed at Lille University Hospital for COVID-19

Head : CHOPIN Marie Charlotte
DEPLANQUE Dominique

Main objective

The primary objective of this study is to identify the predictive factors for mortality at D28 of SARS-CoV-2 infection in patients managed for COVID-19 at Lille University Hospital, via the creation of an epidemiological, clinical, biological, immunological, genetic, microbiological, pathological, radiological and therapeutic database, indicating the results of functional tests.
NB: The analysis will exclude patients who are "confirmed cases" with serious SARS-CoV-2 infection managed in a conventional medicine department owing to the therapeutic limitations (TL) which existed prior to SARS-CoV-2 infection, due to incurable disease or underlying comorbidities.

Inclusion criteria

Any adult patient, "suspect patients", "possible cases", "probable cases" or "confirmed cases" of SARS-CoV-2 infection admitted to Lille University Hospital.

SISCOVID - Observational, prospective, multicentre cohort of patients followed up after hospitalisation to evaluate respiratory sequelae subsequent to SARS-CoV-2 (COVID-19) infection

Head : CALCAIANU George

Version 1
Overview

27

Last update : 05/03/2021

SISCOVID - Observational, prospective, multicentre cohort of patients followed up after hospitalisation to evaluate respiratory sequelae subsequent to SARS-CoV-2 (COVID-19) infection

Head : CALCAIANU George

Main objective

Evaluate the respiratory sequelae after SARS-CoV-2 infection in patients hospitalised for severe COVID-19 pneumonia requiring O2, with subsequent outpatient follow-up (6 months) by:
- Low-dose chest CT scan (LD-chest CT),
- Static lung function tests (LFT),
- Arterial blood gases in ambient air at rest (AA BG) and/or with oxygen (O2 BG),
- 6-minute walking test in ambient air (6WT AA) and/or with oxygen (6WT O2)

Inclusion criteria

Patient having received verbal information and not objecting to the study
Age >= 18 years inclusive
Patient hospitalised for severe COVID-19 pneumonia requiring O2
Patient having contracted SARS-CoV-2 infection proven by RT-PCR and/or retrospective serology and/or COVID-19 syndrome with chest CT scan consistent with infection (over the period from 1 March 2020 to 30 June 2020)

NICORISCOVID - Measurement of the strength of the relationship between tobacco use and the RT-PCR test for SARS-CoV2

Head : KARMOCHKINE Marina, no

Version 1
Overview

28

Last update : 05/05/2021

NICORISCOVID - Measurement of the strength of the relationship between tobacco use and the RT-PCR test for SARS-CoV2

Head : KARMOCHKINE Marina, no

Main objective

Measure the strength of the relationship between tobacco use and the RT-PCR test for SARS-CoV2

Inclusion criteria

Care personnel having attended the Hôtel-Dieu Hospital Covid screening centre for symptoms compatible with SARS-CoV2 infection,
-Aged over 18 years,
With an email address,
-Able to express non-objection (=questionnaire feedback

CERTIFY.HEALTH - Evaluation of the Certify.Health application as a digital resource for managing the COVID-19 pandemic

Head : BOSSON Jean-Luc, TIMC Laboratory - Themas team

Version 1
Overview

29

Last update : 05/05/2021

CERTIFY.HEALTH - Evaluation of the Certify.Health application as a digital resource for managing the COVID-19 pandemic

Head : BOSSON Jean-Luc, TIMC Laboratory - Themas team

Main objective

Evaluate the user-friendliness and acceptability of the Certify.Health application among healthcare personnel in healthcare, research and teaching facilities

Inclusion criteria

- Age ≥ 18 years
- Healthcare personnel in healthcare, research and teaching facilities, or a member of the home-care network:
• equipped with a smartphone which can run the electronic application (version of the participant’s Android or iOS operating system compatible with the application) and having an internet connection OR a computer with internet access
• agreeing to provide their mobile phone number to access the application and receive notifications
OR a resident in a selected nursing home

ComCor - Study of sociodemographic factors, behaviours and practices associated with SARS-CoV-2 infection (ComCor)

Head : Fontanet Arnaud, Emerging Diseases Epidemiology Unit

Version 1
Overview

30

Last update : 05/07/2021

ComCor - Study of sociodemographic factors, behaviours and practices associated with SARS-CoV-2 infection (ComCor)

Head : Fontanet Arnaud, Emerging Diseases Epidemiology Unit

Main objective

Identify the sociodemographic characteristics, places frequented, and behaviours associated with a risk of SARS-CoV-2 infection.

Inclusion criteria

All subjects:
o Adult subject
o Having agreed to take part in the study
o Index case:
o Cases identified in the COVID-19 screening information
system database, SIDEP
o With a positive test for SARS-CoV-2 by
RT-PCR on a nasopharyngeal or throat swab (or
any other sample for which current technology
indicates active infection if positive) within the past 14
days
o Close contact cases:
o Living in the same household (sharing the same
home) as the case having invited him/her to take part
o With a positive test for SARS-CoV-2 by RT-PCR on a nasopharyngeal or
throat swab (or any other sample for which current technology
indicates active infection if positive)
following contact with the index case
o Close contact controls:
o Living in the same household (sharing the same
home) as the case having invited him/her to take part
o With a negative test for SARS-CoV-2 by RT-PCR on a nasopharyngeal or
throat swab (or any other sample for which current technology
indicates active infection if positive)
following contact with the index case
o Distant contact controls:
o Selected by IPSOS based on criteria including age,
gender, and administrative department of residence (paired
with index cases)

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