Study of the Immunological and Virological Response of Patients With COVID-19 and Presenting an Asymptomatic or Pauci-symptomatic Form (AMBUCOV)
NCT04703114 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 57
Last updated 2026-03-27
Summary
The purpose of this study is to describe the immunological and virological response of patients infected with CoV-2-SARS and presenting an asymptomatic or mildly symptomatic form, in particular the innate and adaptive response as well as the virological clearance kinetics.
The research hypothesis is that patients with an ambulatory form of SARS-CoV-2 infection, whether asymptomatic or mildly symptomatic, are able to mount an innate and adaptive immunological response capable of rapidly clearing the virus, in contrast to severe forms in which an early deficit of type 1 IFN response has been demonstrated, possibly responsible for a defect in the control of viral replication in the blood.
Conditions
- Covid19
- SARS-CoV-2
Interventions
- DIAGNOSTIC_TEST
-
Blood count
Blood count at each visit
- DIAGNOSTIC_TEST
-
Blood collection
Blood collection to understanding of the immunological profile at each visit
- DIAGNOSTIC_TEST
-
Nasopharyngeal swab
Research of SARS-CoV-2 infection in nasopharyngeal swab by RT-PCR at day 8 and day 15
- DIAGNOSTIC_TEST
-
Saliva samples
Research of SARS-CoV-2 infection in saliva samples at each visit (excepted inclusion)
- DIAGNOSTIC_TEST
-
Faeces samples
Research of SARS-CoV-2 infection in faeces samples at day 3, day 15 and day 90
- GENETIC
-
Genetic blood collection
Collection to further research at each visit
- OTHER
-
Data collection
Demographics, symptoms, biological constants
Sponsors & Collaborators
-
Fonds IMMUNOV
collaborator UNKNOWN -
URC-CIC Paris Descartes Necker Cochin
collaborator OTHER -
Assistance Publique - Hôpitaux de Paris
lead OTHER
Principal Investigators
-
Solen KERNEIS, Doctor · Assistance Publique - Hôpitaux de Paris
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-02-05
- Primary Completion
- 2021-09-15
- Completion
- 2021-09-15
Countries
- France
Study Locations
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