Actively Recruiting
Prospective Registry of Outcome and Correlates of Chemosensory Dysfunction at the Smell & Taste Clinic of UZ Leuven
Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2025-12-18
500
Participants Needed
1
Research Sites
469 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Smell and taste disorders are common conditions that can greatly affect a person's quality of life. Researchers at UZ Leuven started a specialized clinic in September 2021 to assess patients with these disorders, especially those related to post-COVID-19 effects. This observational study aims to better understand how smell and taste disorders affect people in the Belgian/Flemish population, focusing on how severe the symptoms are, their impact, and how they change over time. Participants receive standard care diagnostic tests and complete structured questionnaires as part of the study. This registry collects data prospectively and retrospectively, using routine clinical evaluations without introducing new treatments. The study follows participants for up to five years to observe changes in their chemosensory functions. During the study, participants will undergo psychophysical tests and fill out questionnaires to assess their smell and taste functions. Researchers will monitor these functions over time to understand the progression and prognosis of these disorders. Participation involves cooperating with tests and providing informed consent. The study does not exclude any participants based on sex, gender, ethnicity, medical history, or prior treatments, and participation can last up to five years.
CONDITIONS
Brief Title
Prospective Registery of Smell/Taste Clinic Ear/Nose/Throat
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The psychophysical testing and questionnaires require a cooperative participant who can understand instructions and communicate choices
- Informed consent is necessary to participate in the prospective registry
You will not qualify if you...
- There are no exclusion criteria related to sex, gender, ethnicity, medical history, or prior treatments
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 5 years
Participants who undergo routine care are observed to assess chemosensory function over time.
Trial Site Locations
Total: 1 location
1
UZ/KU Leuven
Leuven, Vlaams-Brabant, Belgium, 3000
Actively Recruiting
Research Team
M
Marnick Clijsters
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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