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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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ARCHIVES : 309 forms

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Flurec - Recurring influenza virus infections and implications in terms of epidemic recurrences and pandemic risk.

Head : Carrat Fabrice, UMR-S 707 / Epidémiologie des maladies infectieuses et modélisation
De Lamballerie Xavier, UMR-D 190, Emergence des pathologies virales

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91

Last update : 01/01/2020

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Flurec - Recurring influenza virus infections and implications in terms of epidemic recurrences and pandemic risk.

Head : Carrat Fabrice, UMR-S 707 / Epidémiologie des maladies infectieuses et modélisation
De Lamballerie Xavier, UMR-D 190, Emergence des pathologies virales

Main objective

To explore cross-protective immunity involving different A/H1N1 viruses (seasonal and pandemic) and the seasonal A/H3N2 virus through data gathered from this study. This study also aims to identify the epidemiological, immunological and virological factors that determine the risk of recurring influenza infections as well as characterise the population's herd immunity and its evolution.

Inclusion criteria

The "influenza" group comprises of patients enrolled after general medical consultation for influenza-like illness during seasonal epidemic. The "non-influenza" group comprises of patients enrolled after general medical consultation during seasonal epidemic for a reason other than influenza, yet that was acute in nature e.g. infectious diarrhoea, minor trauma.

Last update : 01/01/2020

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- Case-Control Study on the Impact of Bottom-Up and Top-Down Negative Emotion Generation on Memory Formation Among Healthy and Traumatised Adolescents

Head : Guillery-Girard Bérengère, INSERM U1077

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92

Last update : 01/01/2018

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- Case-Control Study on the Impact of Bottom-Up and Top-Down Negative Emotion Generation on Memory Formation Among Healthy and Traumatised Adolescents

Head : Guillery-Girard Bérengère, INSERM U1077

Main objective

The aim of the study is to investigate the influence of bottom-up and top-down processes in the generation of emotions and their effect on attention and memory, and to assess the differential impact of attention deficits on memory through a case-control survey of traumatised adolescents with attentional bias.

Inclusion criteria

- Individuals with a post-traumatic stress disorder with no stress for at least a year;
- Individuals with no other neurological, psychiatric or learning disorders;
- No intellectual disability;
- Not taking medication;
- Native level French;
- Signed consent form (parents and children).

Last update : 01/01/2018

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- Cohort of Patients with Depression: Toxic Effects on Brain Function

Head : Falissard Bruno , Inserm U1018 – Centre for Research in Epidemiology and Population Health – Team: Gender, Sexual and Reproductive Health
Corruble Emmanuelle, INSERM U669 BICETRE UNIVERSITY HOSPITAL – PSYCHIATRIC DEPARTMENT

Version 1
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93

Last update : 01/01/2018

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- Cohort of Patients with Depression: Toxic Effects on Brain Function

Head : Falissard Bruno , Inserm U1018 – Centre for Research in Epidemiology and Population Health – Team: Gender, Sexual and Reproductive Health
Corruble Emmanuelle, INSERM U669 BICETRE UNIVERSITY HOSPITAL – PSYCHIATRIC DEPARTMENT

Main objective

To assess the impact of depression on the hippocampus.

Inclusion criteria

Outpatients from selected physicians who:
– meet the DSM-IV criteria for major depressive disorder based on clinical assessment criteria;
– were tested for delayed memory function during two visits several weeks apart.

Last update : 01/01/2018

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CEPHEUS - Assessment of lipid-lowering treatment in France

Head : Ferrières Jean, Département d'épidémiologie INSERM UMR1027

Version 3
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Overview

94

Last update : 09/05/2017

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CEPHEUS - Assessment of lipid-lowering treatment in France

Head : Ferrières Jean, Département d'épidémiologie INSERM UMR1027

Main objective

Determine the proportion of patients on lipid-lowering drugs who reach the LDL-C goals recommended in guidelines.

Inclusion criteria

man or woman - adult - treated with lipid-lowering drugs for at least three months, with no dose adjustment for a minimum of six weeks

Last update : 09/05/2017

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CESAME - Cancer and Increased Risk Associated with Inflammatory Bowel Disease in France

Head : Beaugerie Laurent, UMRS-S 707

Version 2
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Overview

95

Last update : 12/01/2017

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CESAME - Cancer and Increased Risk Associated with Inflammatory Bowel Disease in France

Head : Beaugerie Laurent, UMRS-S 707

Main objective

General objective: To test the hypothesis that the use of immunosuppressants (IS) for inflammatory bowel disease (IBD) leads to an increased risk of lymphoma in a cohort population. Secondary objective: to assess - relative risk associated with IS treatment for all cancers, to assess the standardised incidence rate for all other cancers observed during IBD; -The increased risk of colorectal cancer associated with extensive and former colonic inflammation for ulcerative colitis (UC) and Crohn's disease: - Increased risk of ileal adenocarcinoma associated with chronic ileal inflammation in Crohn's disease; - Evaluation of mortality of patients with IBD diseases and risk factors; - Protective role of salicylates, pregnancy and malformation syndromes.

Inclusion criteria

Subjects with IBD (Crohn's disease, ulcerative colitis, and indeterminate colitis) defined according to the usual diagnostic criteria, who attended consultation at least once between May 2005 and May 2006.

Last update : 12/01/2017

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ABSINTHE - Observational study of the therapeutic strategy in the management of acute sinusitis in primary care

Head : Moore Nicholas, Service de Pharmacologie, CIC-P 0005-INSERM U657- Université Bordeaux Segalen

Version 2
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Overview

96

Last update : 09/05/2017

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ABSINTHE - Observational study of the therapeutic strategy in the management of acute sinusitis in primary care

Head : Moore Nicholas, Service de Pharmacologie, CIC-P 0005-INSERM U657- Université Bordeaux Segalen

Main objective

The study objectives were to describe the management of acute sinusitis in real-life conditions of prescription and to evaluate the effectiveness of the initial therapeutic strategy.

Inclusion criteria

Patient consulting for acute sinusitis diagnosed according to criteria of the practitioner; Patient without a previous episode of acute sinusitis during the two months preceding diagnosis; Patient aged 18 years and over; Patient agreeing to participate in the study; Patient not included in a clinical trial (Huriet-Sérusclat); Patient who may be followed for two months; Patient showing no severe active disease (life-threatening in the next three months).

Last update : 09/05/2017

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