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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06115291
Other study ID # STUDY00146529
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date February 13, 2020
Est. completion date December 31, 2023

Study information

Verified date October 2023
Source University of Kansas Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To date, there is no validated pharmacotherapy for olfactory disorders. Interestingly, olfactory training - the intentional exposure to odorants for the purposes of retraining the sense of smell - has shown success with as many as 28% of subjects over the course of 12 weeks.


Description:

Study Objectives: The overall, primary goals of these studies are as follows: 1. To compare the outcomes of our olfactory testing battery for olfactory training to the previously published literature 2. To determine if using a larger panel of odorants (our 15 scents versus the 4 scents previously used in the literature) yields a significant difference in olfactory recovery.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 5
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - history of traumatic brain injury - ability to complete objective olfactory tests and comply with olfactory training protocol Exclusion Criteria: - Anyone lower than the age of 18, or greater than the age of 80 - Pregnant women, as sinonasal symptoms and changes in smell can occur in pregnancy and are multifactorial - Patients with poor or questionable compliance, as participation requires daily compliance with study protocol - Patient's that are unable to perform routine follow-up - Patients who are participating in another study during this trial - Patients with dementia, Alzheimer's disease, Parkinson's disease, or other neurocognitive disorders, as these conditions are associated with baseline olfactory dysfunction. - Patients with other systemic conditions known to impact the sinonasal cavity such as Wegener's granulomatosis, Churg Strauss, and immunodeficiency, as their impact on olfaction is unknown - Patients who are allergic to any of the smells or components of our olfactory testing and training

Study Design


Intervention

Other:
Smell Test
Oils are used for each of the different scents. Each scent is administered via an aromatherapy inhaling stick.

Locations

Country Name City State
United States University of Kansas Medical Center Kansas City Kansas

Sponsors (1)

Lead Sponsor Collaborator
University of Kansas Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Olfactory Threshold Changes in olfactory threshold when comparing pre- and post-olfactory training for performance in terms of percent correct per specific scent and overall combination of percent correct for all tested scents Change from baseline to month 6
Primary Olfactory Identification Changes in ability to detect and identify scents when comparing pre- and post-olfactory training for percent detected per individual scents and as a composite score reflecting performance on all scents Change from baseline to month 6
Secondary Tolerance with Olfactory Training Protocol Self-reported tolerance with following olfactory training protocol At follow-up visits
Secondary Neurocognition Assessment of neurocognition and impact on olfactory quality of life using the Mini-Mental Status Exam (MMSE) and Montreal Cognitive Assessment (MoCA) Change from baseline to month 6
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