NCT06456008

Brief Summary

Smell/taste disorders are common conditions with a significant impact on quality of life. In September 2021, a specific consultation for patients with smell and taste disorders was initiated at the ENT-HNS (ear, nose, and throat, head and neck surgery) department of UZ Leuven, partly in light of post-COVID-19 related smell disorders. With this observational ambidirectional study, the investigators aim to better map smell/taste disorders in the Belgian/Flemish population. Using standard-of-care diagnostic tests and structured questionnaires, the investigators strive to gain more insight into the severity, impact, and progression/prognosis of smell/taste disorders.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
116mo left

Started Dec 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress27%
Dec 2022Dec 2035

Study Start

First participant enrolled

December 6, 2022

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

June 6, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

June 13, 2024

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2035

Last Updated

December 18, 2025

Status Verified

December 1, 2025

Enrollment Period

4.1 years

First QC Date

June 6, 2024

Last Update Submit

December 9, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Chemosensory function

    Observational up to 5 years follow-up

Interventions

Standard of care

Eligibility Criteria

Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients consulting for chemosensory dysfunction

You may qualify if:

  • The psychophysical testing as well as the questionnaires require a cooperative participant who can understand and follow instructions and communicate their choices.
  • Informed consent is necessary upon participation for prospective registry.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UZ/KU Leuven

Leuven, Vlaams-Brabant, 3000, Belgium

RECRUITING

MeSH Terms

Conditions

Taste DisordersOlfaction Disorders

Interventions

Standard of Care

Condition Hierarchy (Ancestors)

Sensation DisordersNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Quality Indicators, Health CareQuality of Health CareHealth Services AdministrationHealth Care Quality, Access, and Evaluation

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
5 Years
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 6, 2024

First Posted

June 13, 2024

Study Start

December 6, 2022

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

December 31, 2035

Last Updated

December 18, 2025

Record last verified: 2025-12

Locations