Study of the Kinetics of the Immune Response During the Intensive Care Unit Stay in Adult Patients Infected With SARS-CoV-2: Multicentric Non Interventional Study

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Biological
Study Type: Observational
SUMMARY

Infection with the SARS-CoV-2 coronavirus (COVID-19) has recently been identified as a pandemic due to the speed and global scale of its transmission. In Auvergne-Rhône-Alpes region (AURA), the epidemic began in February 2020 and the number of infected people is still important. Between 15 and 20% of COVID-19 patients develop an acute respiratory distress syndrome (ARDS) leading to their hospitalization in intensive care. Their clinical progression can be rapidly harmful with the development of severe ARDS associated with an increased risk of death. Preliminary data on the immune response of COVID-19 patients describe the induction of a moderate inflammatory response and the occurrence of major progressive lymphopenia over time associated with potential immunosuppression. Up to 50% of secondary infections are reported in deceased COVID-19 patients. However, no prospective study has exhaustively described the kinetics of the immune response of COVID-19 patients in intensive care. The precise description of the immune response over time in adult patients with a proven infection with the SARS-CoV-2 virus and the study of the relation between this response and the increased risk of organ failure (severe ARDS), death or nosocomial infection will allow us to better understand the pathophysiology of the immune response induced by COVID-19 in order to (i) identify new therapeutic strategies targeting the host response in patients in intensive care (ii) to develop biological markers to stratify patients for future clinical trials evaluating these immunoadjuvant treatments in COVID-19.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Man or woman aged 18 or over,

• Hospitalization in intensive care for Sars-Cov-2 pneumopathy,

• First hospitalization in intensive care unit,

• Positive diagnosis of SARS-CoV2 infection carried out by PCR or by another approved method in at least one respiratory sample,

• Sampling in the first 24 hours after admission to intensive care unit (D0 / D1) feasible,

• Patient or next of kin who has been informed of the terms of the study and has not objected to participating.

Locations
Other Locations
France
Hôpital Pierre Wertheimer
RECRUITING
Bron
Hôpital Gabriel Montpied
NOT_YET_RECRUITING
Clermont-ferrand
Centre hospitalier universitaire de Grenoble Alpes
NOT_YET_RECRUITING
Grenoble
Hôpial de la Croix Rousse
RECRUITING
Lyon
Hôpital Edouard Herriot
RECRUITING
Lyon
Hôpital Edouard Herriot
RECRUITING
Lyon
Hôpital Lyon Sud
RECRUITING
Pierre-bénite
CH de St Etienne
NOT_YET_RECRUITING
Saint-etienne
Contact Information
Primary
Fabienne VENET
fabienne.venet@chu-lyon.fr
4 72 11 97 46
Backup
Marie GROUSSAUD
marie.groussaud@chu-lyon.fr
4 72 35 71 70
Time Frame
Start Date: 2020-05-11
Estimated Completion Date: 2026-04
Participants
Target number of participants: 200
Treatments
Cohort
Patients over 18 years with a confirmed diagnosis of COVID 19 hospitalized in intensive care unit
Sponsors
Collaborators: BioMérieux
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov