Study of the Evolution of Olfactory Disorders in Patients With Persistent Loss of Smell Following COVID-19 (ETOC)

Pasteur Institute

Status: Enrolling

Conditions: SARS-CoV-2 Acute Respiratory Disease

Treatments: Other: Clinical examination; Other: Olfactory evoked potentials; Other: Nasal endoscopy; Other: Neurological examination and neuropsychological assessment; Other: Brushing of olfactory slits; Other: Assessment of olfactory and taste functions; Other: Blood collection

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05133596

2021-A02419-32 (Other Identifier)

2021-006

Details and patient eligibility

About

The COVID-19 pandemic is a novel medical challenge, particularly because of the systemic nature of this disease. Indeed, COVID-19 affects several organs and systems at once. The brain is affected in several ways: direct infection of nerve cells by SARS-CoV-2, inflammation of the central nervous system, severe systemic inflammation damaging nerve cells, global cerebral ischaemia related to respiratory failure, thromboembolic events related to increased intravascular coagulation and severe psychological stress. As a result, COVID-19 sometimes manifests as neurological and neuropsychiatric symptoms such as dizziness, sleep disturbances, cognitive deficits, delirium, or severe depression.

Sudden loss of smell is a common symptom associated with COVID-19 and SARS-CoV-2 infection of neurons in the olfactory system has been reported in both hamsters and humans. The vast majority of COVID-19 patients recover their olfactory function within a few weeks. However, a significant minority of infected individuals (1 in 5 cases) still suffers from olfactory disorders (anosmia, hyposmia and/or parosmia) several months after the primary infection. These olfactory disorders are frequently associated with depressive behaviour and cognitive complaints. In PET scans, it is even possible to correlate this cognitive dysfunction with hypometabolism of certain brain regions, including the olfactory gyrus.

This project proposes, during one year, to evaluate and follow the evolution of the olfactory capacities of patients suffering from persistent smell disorder since one year (+/- 4 months) following COVID-19. The issue is to study the link between viral persistence in the olfactory sensory organ, chronic inflammation, and central damage to the olfactory system. The follow-up of the evolution of olfactory and neurocognitive capacities, in an integrative way by means of molecular, physiological and behavioural approaches, will inform us on the specificities of "COVID-long" and on the level of peripheral and/or central damage of the olfactory system.

Full description

Prospective monocentric descriptive study. Evaluation of COVID-19 patients with persistent loss of smell during 2 visits at 1 year intervals (V1 and V2).

V1 :The following examinations will be carried out specifically for the research.

• Clinical examination;
• Blood sampling;
• Recording of olfactory evoked potentials;
• Neurological examination and neuropsychological assessment;

V2 :

All examinations performed at V1 will be repeated at V2.

If the following examinations are not carried out during care within 3 weeks of V2, they will be carried out as part of the research during this V2 visit.

• Nasal endoscopy ;
• Assessment of olfactory and gustatory functions.

The following explorations will be carried out:

• Passing of two olfactory and gustatory scales; Olfactory and gustatory disorders will be quantified using two scales, the visual analogue scale VAS and the modified TSS;
• Sniffin Stick test.

In addition, MRI data from clinical care will be collected.

Enrollment: 30 estimated patients

Sex: All

Ages: 18 to 55 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adults < 55 years
• History of symptomatic COVID over 1 year +/- 4 months with a positive PCR diagnosis of SARS-CoV-2
• Olfactory complaint
• Able to understand simple questionnaires in French.
• Subject covered by French Social Security (except for Aide Médicale d'Etat).

Exclusion criteria

• Contraindication to nasal swabbing (for morphological reasons, haemostasis disorders, taking aspirin in the 15 days prior to swabbing or anticoagulants, contraindications to the use of a local anaesthetic such as a history of allergy to local anaesthetics or any other reasons judged by the clinical investigator)
• To have been placed in the intensive care unit following COVID-19.
• Known previous nasal-sinus pathology.
• History of psychiatric pathology according to DSM IV criteria, ischaemic, neoplastic, inflammatory, infectious or neurodegenerative (meningitis, encephalopathy, encephalitis, stroke, neurodegenerative disease) known or suspected.
• History of loss of sense of smell prior to COVID infection.
• Patient affiliated to the Aide Médicale d'Etat.
• Person deprived of liberty by judicial or administrative decision, or subject to legal protection.

Trial design

Primary purpose: Basic Science

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

Study population

Experimental group

Description:

Adult subjects up to 55 years of age with persistent olfaction disorder after a symptomatic episode of COVID-19.

Treatment:

Other: Neurological examination and neuropsychological assessment

Other: Assessment of olfactory and taste functions

Other: Brushing of olfactory slits

Other: Nasal endoscopy

Other: Blood collection

Other: Olfactory evoked potentials

Other: Clinical examination