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HLA-G Immuno-Inhibitor Checkpoint Study in Patients With COVID-19 Infection: Molecular and Cellular Assessment (HLA-G-COVID)

H

Hopital Foch

Status

Completed

Conditions

Covid19

Treatments

Other: Baseline blood sample
Other: Baseline and during hospitalization blood samples

Study type

Interventional

Funder types

Other

Identifiers

NCT04613297
2020_0082

Details and patient eligibility

About

The aim of the research is to study the immune checkpoint linked to the HLA-G molecule in the dysregulation of the control of COVID-19 infection.

Full description

Single-center, prospective, open-ended, interventional study with minimal risks and constraints. Patients will be divided into 3 groups: patients not infected with COVID-19, patients infected with COVID-19 not hospitalized, patients infected with COVID-19 hospitalized.

Enrollment

91 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with possible or confirmed infection by COVID-19

Exclusion criteria

  • Patient without liberty or guardianship

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

91 participants in 3 patient groups

COVID-19 uninfected patients
Other group
Description:
Patient with negative PCR result
Treatment:
Other: Baseline blood sample
non-hospitalized COVID-19 infected patients
Other group
Description:
Patient with positive PCR result who does not require hospitalization for COVID-19
Treatment:
Other: Baseline blood sample
hospitalized COVID-19 infected patients
Other group
Description:
Patient with positive PCR who require hospitalization for COVID-19
Treatment:
Other: Baseline and during hospitalization blood samples

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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