Official Title
Rapid Detection of COVID-19 by Portable and Connected Biosensor : Biological Proof of Concept
Brief Summary

The objective of study is to estimate the sensitivity and specificity of the COR-DIAL based on nasopharyngeal samples taken at the patient's admission in relation to the final diagnosis of COVID-19 made by the medical team.


Diagnostic Test: COVID-19 RT-PCR

Nasopharyngeal swabs for COVID-19 RT-PCR

Diagnostic Test: Biosensor

Portable and Connected Biosensor viral

Eligibility Criteria

Inclusion Criteria:

- Male or female or child without age limit

- Admitted to a Reference Health Establishment in an emergency unit, hospitalisation or
intensive care unit for suspicion of SARS-CoV-2 infection, regardless of the clinical
presentation and degree of severity.

- Patient to be diagnosed using a PCR test on nasopharyngeal swab.

- Social insured

Exclusion Criteria:

- Atypical or suspicious cases without a final diagnosis of COVID-19 positive or

- Patient refusal to participate

Eligibility Gender
Eligibility Age
Minimum: N/A ~ Maximum: N/A

CHU lille
Lille, France

Investigator: Enagnon-Kazali ALIDJINOU, MD


Enagnon Kazali ALIDJINOU, MD
(0) - +33

David Devos, MD,PhD

Enagnon Kazali ALIDJINOU, MD, Principal Investigator
University Hospital, Lille

University Hospital, Lille
NCT Number