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

No results posted yet for this study

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

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

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04703114 on ClinicalTrials.gov