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Collection of Biological Samples With Clinical Characterization of Covid-19 Patients

Not Applicable
Terminated
Conditions
Covid-19
Interventions
Biological: Biological test
Registration Number
NCT04363385
Lead Sponsor
Centre Hospitalier Intercommunal Creteil
Brief Summary

Biological collection (blood sample) associated with clinical data from Covid-19 patients

Detailed Description

SARS-Cov2 is an emerging respiratory virus in the coronavirus family, responsible of the pandemic since November 2019. France, which has more than 17,000 deaths from the virus, is one of the main outbreaks. As of 16 April 2020, more than 76,000 individuals in France have been hospitalized, corresponding to 69% of confirmed cases (https://www.santepubliquefrance.fr).

Most affected patients have more or less marked clinical signs associating fever, cough, dyspnea, myalgia, anosmia, ageusia, digestive disorders. In some cases, the progression is worse with lung disease of varying severity. Indications for hospitalization are essentially the severe forms of Covid-19 disease, characterized by hypoxemic lung disease.

Risk factors for developing severe Covid-19 disease have been identified already: age, co-morbidity such as diabetes, obesity-overweight or cardiovascular diseases. It is assumed that other host-related factors, including genetics, may contribute to the existence of this phenotypic heterogeneity. At present, these factors are not known.

The objective of this research is to constitute a DNA collection from patients with Covid-19, in order to be able to search for genetic factors modulating the clinical phenotype.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
500
Inclusion Criteria
  • Diagnosis of COVID-19 confirmed on RT-PCR test or chest scanner
  • Any age
  • Membership in the general social security system
  • Inform consent signed by the patient or by legal representatives for minors
Exclusion Criteria
  • Refusal of the patient or one of the legal representatives

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Collection of blood sampleBiological test-
Primary Outcome Measures
NameTimeMethod
Phenotype/genotype correlation research modulating the severity of Covid-19 diseaseAnytime in the period of 10 years

Clinical aggravation markers (admission in intensive care)

Secondary Outcome Measures
NameTimeMethod
Phenotype/transcriptomic correlation research modulating the severity of Covid-19 diseaseAnytime in the period of 10 years

Severity at the Covid-19 Lung Scanner

Development of predictive imaging scores in the severity of Covid-19 diseaseAnytime in the period of 10 years

Evolution of scanographic lesions or pulmonary ultrasound

Development of clinical-biological scores in the severity of Covid-19 diseaseAnytime in the period of 10 years

Evolution of scanographic lesions or pulmonary ultrasound

Phenotype/biomarker correlation research modulating the severity of Covid-19 diseaseAnytime in the period of 10 years

Severity at the Covid-19 Lung Scanner

Identification of transcriptomic markers for treatment responseAnytime in the period of 10 years

Sequencing transcriptome

Identification of pathophysiological pathways to susceptibility to Covid-19 diseaseAnytime in the period of 10 years

Duration of oxygen therapy, artificial ventilation

Identification of genetic markers for treatment responseAnytime in the period of 10 years

Genome sequencing

Identification of proteomic for treatment responseAnytime in the period of 10 years

Proteomic sequencing

Trial Locations

Locations (1)

Centre hospitalier intercommunal de Créteil

🇫🇷

Créteil, France

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