Prospective Registery of Smell/Taste Clinic Ear/Nose/Throat
ProspeRo'Scent
Prospective Registry of Outcome and Correlates of Chemosensory Dysfunction at the Smell & Taste Clinic of UZ Leuven
1 other identifier
observational
500
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2022
Longer than P75 for all trials
1 active site
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 Start
First participant enrolled
December 6, 2022
CompletedFirst Submitted
Initial submission to the registry
June 6, 2024
CompletedFirst Posted
Study publicly available on registry
June 13, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2035
December 18, 2025
December 1, 2025
4.1 years
June 6, 2024
December 9, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Chemosensory function
Observational up to 5 years follow-up
Interventions
Standard of care
Eligibility Criteria
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
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
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