search
Back to results

Investigation of the Persistence of SARS-CoV-2 in the Olfactory Mucosa of Patients With Prolonged Symptoms of COVID-19 (NEUROCOVID)

Primary Purpose

SARS-CoV-2 Infection, Cognitive Disorder

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Nasopharyngeal swab for RT-PCR SARS-CoV-2
Sponsored by
Fondation Ophtalmologique Adolphe de Rothschild
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for SARS-CoV-2 Infection

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Other

Other

Arm Label

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

Arm Description

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

Outcomes

Primary Outcome Measures

Presence of SARS-CoV-2 RNA in the olfactory mucosa
Comparison of the presence of SARS-CoV-2 RNA in the olfactory mucosa between cases and controls

Secondary Outcome Measures

Full Information

First Posted
February 1, 2022
Last Updated
February 11, 2023
Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Collaborators
Hotel Dieu Hospital, Institut Pasteur, Hôpital Lariboisière Fernand Widal
search

1. Study Identification

Unique Protocol Identification Number
NCT05220241
Brief Title
Investigation of the Persistence of SARS-CoV-2 in the Olfactory Mucosa of Patients With Prolonged Symptoms of COVID-19
Acronym
NEUROCOVID
Official Title
Investigation of the Persistence of SARS-CoV-2 in the Olfactory Mucosa of Patients With Prolonged Symptoms of COVID-19 With Neurocognitive Complaints: a Prospective Cross-sectional Multicenter Case / Control Study (NEUROCOVID)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2022 (Actual)
Primary Completion Date
July 1, 2023 (Anticipated)
Study Completion Date
July 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Collaborators
Hotel Dieu Hospital, Institut Pasteur, Hôpital Lariboisière Fernand Widal

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
NEUROCOVID is a prospective multicenter study comparing the proportion of patients with SARS-CoV-2 viral RNA at the level of the olfactory clefts in a group of cases compared to a group of controls as well as the correlations between the virological and cellular abnormalities observed in the olfactory mucosa and the severity of the clinical neurological profile
Detailed Description
More than 15% of people who developed COVID-19 would still have at least one symptom six months older. In France, this would concern several hundred thousand people. The societal consequences are important. The symptoms are very polymorphic; they evolve in a fluctuating fashion and persist for several months. Neurological symptoms are often in the foreground and include different symptoms, among which: Cognitive disorders (psychic slowing down, lack of clarity in thought, difficulty in remembering certain facts, difficulty in performing double tasks, difficulty in finding words). Sensory disturbances such as burning or tingling with or without root topography, dizziness. Neurovegetative manifestations: sudden tachycardia, palpitations, vasomotor disorders, excessive sweating, digestive disorders or post prandial malaise, feelings of malaise (lipothymia with or without hypotension), dyspnea or a feeling of dyspnea, urinary disorders Sleep disorders (insomnia, sleep fragmentation, nightmares or hypersomnia) Tension type headaches. The mechanisms explaining the occurrence of these symptoms are still debated. An important result is the recent demonstration by the UK's National Statistics Office that people with "long COVID" may, for some, remain carriers of the SARS-CoV-2 virus for several months. So far, viral persistence has only been demonstrated in a few specific cases of immunocompromised people, almost all of them having been hospitalized. Recently, in a pilot study conducted jointly by the Institut Pasteur and AP-HP, we demonstrated that viral RNA could be found in immunocompetent patients with prolonged neurological symptoms after COVID-19 (Melo et al 2021). This study concerned 4 patients explored by micro-brushing the mucous membrane of the olfactory cracks under local anesthesia more than 4 months after the initial COVID-19. In all patients, SARS-CoV-2 RNA persisted in significant amounts. Although this demonstration currently only concerns a small number of people, this study provides evidence that the virus can remain hidden in the olfactory cracks (a tissue that is part of the nervous system), including in people with PCR nasopharyngeal and / or SARS-CoV-2 serology become negative. This persistence of the virus after a so-called "acute" infection is not unique. In EBOLA virus disease, some people have been shown to keep the virus in their semen for several months. It is now necessary to determine whether this persistence is specific to long COVID, what are the mechanisms and the consequences of this persistence of the virus. One of the hypotheses is that the virus would persist in endothelial cells and / or support cells. Intermittent reactivation of the virus would lead to intermittent inflammation, secretion of pro-inflammatory cytokines, activation of coagulation and innate immunity cells (monocytes, mast cells, astrocytes, cerebral glial cells) or adaptive This activation could be due to origin of possible micro-thrombosis responsible for a decrease in the oxygen supply in the tissues. This tissue hypoxia could cause the intermittent "brain fog" complained about by patients and the cerebral hypo-metabolisms seen on CT scans. The virus could infect other cells as well, and the issue of direct infection of neurons remains unresolved. In this study, we want to assess whether viral persistence is specific to patients with prolonged symptoms following COVID-19, to assess whether the presence of SARS-CoV-2 RNA is correlated with the ability of the virus to replicate, study the cellular abnormalities associated with the presence of viruses, and correlate the observed cellular and virological abnormalities with the clinical profile of patients. We are interested in central neurological disorders, in particular cognitive disorders, because they are often in the foreground, and they are by far the most disabling symptoms for patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
SARS-CoV-2 Infection, Cognitive Disorder

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Case : patient with 1st episode of COVID-19 and persistence of neurocognitive complaint
Arm Type
Other
Arm Description
Patient with a 1st episode of COVID-19 in the 12 months preceding inclusion and presenting persistence of neurocognitive complaint beyond 4 weeks
Arm Title
Control : Patient with a 1st episode of COVID-19 cured and without neurocognitive complaint
Arm Type
Other
Arm Description
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
Intervention Type
Biological
Intervention Name(s)
Nasopharyngeal swab for RT-PCR SARS-CoV-2
Other Intervention Name(s)
Blood sample for SARS-CoV-2 serology, MoCA (Control only), Ask the 3 questions from the Catherine Thomas-Antérion scale to search for a neurocognitive complaint (Control only)
Intervention Description
2 nasal swabs (one per nostril) of olfactory mucosa cells under local anesthesia for SARS-CoV-2 RT-PCR and pathological analysis
Primary Outcome Measure Information:
Title
Presence of SARS-CoV-2 RNA in the olfactory mucosa
Description
Comparison of the presence of SARS-CoV-2 RNA in the olfactory mucosa between cases and controls
Time Frame
Inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amélie Yavchitz, MD, PhD
Phone
0033148036454
Email
ayavchitz@for.paris
First Name & Middle Initial & Last Name or Official Title & Degree
Lucia Lopes
Email
llopes@for.paris
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mathieu Veyrat, Dr
Organizational Affiliation
Hôpital Fondation A. de Rothschild
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Lariboisière-Fernand-Widal
City
Paris
ZIP/Postal Code
75010
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Charlotte Hautefort, Dr
Email
charlotte.hautefort@aphp.fr
Facility Name
Hôpital Fondation A. de Rothschild
City
Paris
ZIP/Postal Code
75019
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mathieu Veyrat, Dr
Phone
+331 48 03 73 67
Email
mveyrat@for.paris

12. IPD Sharing Statement

Learn more about this trial

Investigation of the Persistence of SARS-CoV-2 in the Olfactory Mucosa of Patients With Prolonged Symptoms of COVID-19

We'll reach out to this number within 24 hrs