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NCT06456008 Clinical Trial

Prospective Registery of Smell/Taste Clinic Ear/Nose/Throat

Olfactory Disorder Clinical Trial

— ProspeRo'Scent  

Official title:
Prospective Registry of Outcome and Correlates of Chemosensory Dysfunction at the Smell & Taste Clinic of UZ Leuven

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06456008
Other study ID # S67158
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 6, 2022
Est. completion date December 31, 2035

Study information
Verified date August 2023
Source Universitaire Ziekenhuizen KU Leuven
Contact Marnick Clijsters
Phone 003216348044
Email marnick.clijsters@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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, we aim to better map smell/taste disorders in the Belgian/Flemish population. Using standard-of-care diagnostic tests and structured questionnaires, we strive to gain more insight into the severity, impact, and progression/prognosis of smell/taste disorders.

Recruitment information / eligibility
Status Recruiting
Enrollment 500
Est. completion date December 31, 2035
Est. primary completion date January 1, 2025
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility 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. There are no exclusion criteria related to sex, gender, or ethnicity. There are no exclusion criteria related to medical history or prior treatments. This study conveys no additional risks for care groups such as pregnant women, or elderly

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Standard of care
Standard of care

Locations
Country Name City State
Belgium UZ/KU Leuven Leuven Vlaams-Brabant

Sponsors (1)
Lead Sponsor Collaborator
Universitaire Ziekenhuizen KU Leuven

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Chemosensory function Observational up to 5 years follow-up
See also
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