Rapid Detection of COVID-19 by Portable and Connected Biosensor

Rapid Detection of COVID-19 by Portable and Connected Biosensor : Biological Proof of Concept

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.

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 negative
• Patient refusal to participate