Investigation of the Persistence of SARS-CoV-2 in the Olfactory Mucosa of Patients With Prolonged Symptoms of COVID-19 (NEUROCOVID)
SARS-CoV-2 Infection, Cognitive Disorder
About this trial
This is an interventional other trial for SARS-CoV-2 Infection
Eligibility Criteria
Inclusion Criteria:
Common to cases and controls:
- Age ≥ 18 years old and <60 years old
- Good oral and written command of French
- Level of education ≥ 7 years of schooling
- Initial episode of COVID-19 within 2 to 12 months
- Symptomatic initial episode of COVID-19
- Initial symptoms not explained by another diagnosis
- Initial episode documented by RT-PCR positive for SARS-CoV-2 and / or positive antigen test and / or positive serology (in the absence of vaccination)
- Express consent to participate in the study
- Affiliate or beneficiary of a social security scheme
Case group:
- Presence of at least one of the initial symptoms beyond 4 weeks following the onset of the acute phase of the disease
- Prolonged symptoms not explained by another diagnosis with no known link to COVID-19
- Neurocognitive complaint (s) previously objectified by a neurologist and after completion of a neuro-psychological assessment
- Impact of neurocognitive disorders on daily life authenticated by a Glasgow outcome scale extended ≤ 7 (see appendix 1)
- Evolution of complaints for 2 to 12 months compared to the date of their first appearance
Exclusion Criteria:
Exclusion criteria common to cases and controls:
- Person benefiting from a legal protection measure
- Pregnant or breastfeeding woman
At least one neurological pathology among:
- encephalopathy
- encephalitis
- severe neurological form of the initial episode of COVID-19
- neurodegenerative disease
- History of stroke
- Serious psychiatric history
- Known nasal sinus pathology
- Hemostatic disorder
- Taking aspirin in the 15 days preceding the sample
- Treatment with anticoagulants
- Known allergy to lidocaine
Secondary exclusion criteria for controls:
- Positive SARS-CoV-2 RT-PCR on nasopharyngeal sample on the day of inclusion
Sites / Locations
- Hôpital Lariboisière-Fernand-Widal
- Hôpital Fondation A. de RothschildRecruiting
Arms of the Study
Arm 1
Arm 2
Other
Other
Case : patient with 1st episode of COVID-19 and persistence of neurocognitive complaint
Control : Patient with a 1st episode of COVID-19 cured and without neurocognitive complaint
Patient with a 1st episode of COVID-19 in the 12 months preceding inclusion and presenting persistence of neurocognitive complaint beyond 4 weeks
Patient with a cured 1st episode of COVID-19 (without persisting symptoms beyond 4 weeks) in the 12 months preceding inclusion and without neurocognitive complaint