SARS-CoV-2 InfectionNEUROCOVIDNCT05220241
Investigation of the Persistence of SARS-CoV-2 in the Olfactory Mucosa of Patients With Prolonged Symptoms of COVID-19
A study testing Nasopharyngeal swab for RT-PCR SARS-CoV-2 in people with SARS-CoV-2 Infection and Cognitive Disorder, run by Fondation Ophtalmologique Adolphe de Rothschild at 2 sites in France.
Trial 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… Read more about this study
- Who is it for?
- Ages 18 to 60 years
- Conditions the study is for
- SARS-CoV-2 Infection, Cognitive Disorder
- What is being tested?
- Nasopharyngeal swab for RT-PCR SARS-CoV-2
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 51 participants
- Where
- 2 sitesFrance
- Study dates
- 1 Jul 2022to 10 Jul 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- 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
Show all 16Show fewer
- 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
Who cannot join
- 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
Show all 16Show fewer
- 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
Trial locations and contacts
2 sites in 1 country.
France2 sites
Hôpital Lariboisière-Fernand-Widal
Paris, 75010
Hôpital Fondation A. de Rothschild
Paris, 75019
About this study
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)
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
Read the 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.
- Conditions
- SARS-CoV-2 Infection, Cognitive Disorder
- Being tested
- Nasopharyngeal swab for RT-PCR SARS-CoV-2
- Medical subject headings
- COVID-19, Cognitive Dysfunction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Nasopharyngeal swab for RT-PCR SARS-CoV-2Biological
Also called 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)
2 nasal swabs (one per nostril) of olfactory mucosa cells under local anesthesia for SARS-CoV-2 RT-PCR and pathological analysis
| Study group | Role | What they receive |
|---|---|---|
| Case : patient with 1st episode of COVID-19 and persistence of neurocognitive complaint | Other | Patient with a 1st episode of COVID-19 in the 12 months preceding inclusion and presenting persistence of neurocognitive complaint beyond 4 weeks Receives: Biological: Nasopharyngeal swab for RT-PCR SARS-CoV-2 |
| Control : Patient with a 1st episode of COVID-19 cured and without neurocognitive complaint | Other | 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 Receives: Biological: Nasopharyngeal swab for RT-PCR SARS-CoV-2 |
What is being measured
The primary outcome is the main question the study is designed to answer.
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
Measured: Inclusion
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Feb 2022
- Study start1 Jul 2022
- Primary completion20 Jun 2025
- Study completion10 Jul 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SARS-CoV-2 InfectionStudies of the same condition, open and under way.
- More trials run by Fondation Ophtalmologique Adolphe de RothschildThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 51 participants (actual)
Sponsor and investigators
- Lead sponsor
- Fondation Ophtalmologique Adolphe de Rothschild
- Sponsor type
- Research network
- Collaborators
- Hotel Dieu Hospital, Institut Pasteur, Hôpital Lariboisière Fernand Widal
- Responsible party
- Sponsor
- Investigators
- Mathieu Veyrat, Dr, Principal investigator, Hôpital Fondation A. de Rothschild
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05220241
- Sponsor's protocol ID
- MVT_2021_26
- Acronym
- NEUROCOVID
- Status last verified
- Dec 2025
- First submitted
- 1 Feb 2022
- Last updated
- 17 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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)
- ClinicalTrials.gov ID
- NCT05220241
- Acronym / sponsor ID
- NEUROCOVID / MVT_2021_26
- Conditions
- SARS-CoV-2 Infection, Cognitive Disorder
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 51 participants (actual)
- Lead sponsor
- Fondation Ophtalmologique Adolphe de RothschildResearch network
- Collaborators
- Hotel Dieu Hospital, Institut Pasteur, Hôpital Lariboisière Fernand Widal
- Study start
- 1 Jul 2022 (actual)
- Primary completion
- 20 Jun 2025 (actual)
- Study completion
- 10 Jul 2025 (actual)
- First posted
- 2 Feb 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Case : patient with 1st episode of COVID-19 and persistence of neurocognitive complaint | Other | Biological: Nasopharyngeal swab for RT-PCR SARS-CoV-2Patient with a 1st episode of COVID-19 in the 12 months preceding inclusion and presenting persistence of neurocognitive complaint beyond 4 weeks |
| Control : Patient with a 1st episode of COVID-19 cured and without neurocognitive complaint | Other | Biological: Nasopharyngeal swab for RT-PCR SARS-CoV-2Patient with a cured 1st episode of COVID-19 (without persisting symptoms beyond 4 weeks) in the 12 months preceding inclusion and without neurocognitive complaint |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (16 listed)
- 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
Key exclusion criteria (16 listed)
- Person benefiting from a legal protection measure
- Pregnant or breastfeeding woman
- At least one neurological pathology among:
- History of stroke
- Serious psychiatric history
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Nasopharyngeal swab for RT-PCR SARS-CoV-2Also: 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)2 nasal swabs (one per nostril) of olfactory mucosa cells under local anesthesia for SARS-CoV-2 RT-PCR and pathological analysis | Biological | 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 |
Primary outcome
Presence of SARS-CoV-2 RNA in the olfactory mucosa
Time frame: Inclusion
Comparison of the presence of SARS-CoV-2 RNA in the olfactory mucosa between cases and controls
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Dec 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mathieu Veyrat, Dr principal investigator
Hôpital Fondation A. de Rothschild
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Nasopharyngeal swab for RT-PCR SARS-CoV-2 in people with SARS-CoV-2 Infection and Cognitive Disorder, run by Fondation Ophtalmologique Adolphe de Rothschild at 2 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 16 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Presence of SARS-CoV-2 RNA in the olfactory mucosa (time frame: Inclusion). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Dec 2025.