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Japanese version of the method for assessment of retronasal olfactory functio

Not Applicable
Conditions
olfactory dysfunction
Registration Number
JPRN-UMIN000040379
Lead Sponsor
ippon Medical school
Brief Summary

19 healthy controls and 32 olfactory dysfunction patients were enrolled in this study. Retronasal odor identification function was assessed with oral taste powders. Validity analysis revealed that the 13 taste powders differentiated between normosmic participants and olfactory dysfunction patients. Based on our findings, we advocate 10 points of taste powders test as the cut-off point between patients and controls.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
41
Inclusion Criteria

Not provided

Exclusion Criteria

pregnant or lactating women, people who have food allergy or food intake regulation due to religious or health condition.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the validity of the method of retronasal olfactory dysfunction.
Secondary Outcome Measures
NameTimeMethod
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