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ANalyzing Olfactory Dysfunction Mechanisms In COVID-19

ANalyzing Olfactory Dysfunction Mechanisms In COVID-19

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04445597
Acronym
ANOSMIC-19
Enrollment
150
Registered
2020-06-24
Start date
2020-05-07
Completion date
2024-12-31
Last updated
2023-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

SARS-CoV-2

Keywords

Hyposmia, Anosmia, Olfactory Dysfunction, COVID-19, SARS-CoV-2

Brief summary

We aim to understand the mechanism of olfactory dysfunction in COVID-19.

Detailed description

In December 2019, a new coronavirus causing severe acute respiratory syndrome was described in Wuhan, China. This virus, later named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), spread worldwide and has been designated a pandemic by the World Health Organization. By the beginning of March 2020, several Ear, Nose, Throat societies raised awareness of a frequent association between coronavirus disease 2019 (COVID-19) and smell disorders. In the present study, the investigators wish to begin to understand the pathogenesis of olfactory dysfunction in COVID-19.

Interventions

OTHERSampling of tissue

In all groups of participants, tissue from the nasal cavity and olfactory system will be surgically removed

Sponsors

Max Planck Research Unit for Neurogenetics
CollaboratorUNKNOWN
AZ Sint-Lucas Brugge
CollaboratorOTHER
Universitair Ziekenhuis Brussel
CollaboratorOTHER
Hospital Clinic of Barcelona
CollaboratorOTHER
Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

\- Deceased hospitalised patients, tested positive or negative for SARS-CoV-2 for patient or control group respectively

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of SARS-CoV-2 in the sampled tissueImmediately after deathIn the sampled tissues, the investigators will determine presence of SARS-CoV-2 by means of immunohistochemistry, RNA-scope and spatial transcriptomics

Countries

Belgium

Contacts

Primary ContactLaura Van Gerven
laura.vangerven@uzleuven.be+3216336342
Backup ContactMarnick Clijsters
marnick.clijsters@kuleuven.be+3216336342

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026