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Objective olfaction test with olfacto-scintigraphy

Not Applicable
Recruiting
Conditions
Olfactory dysfunction
Registration Number
JPRN-jRCTs041180021
Lead Sponsor
Shiga Hideaki
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

1) Patients with olfactory dysfunction
2) Patients aged 20 years old or more
3) Gender unquestioned
4) Outpatient
5) Patients who have given voluntary written informed consent.

Exclusion Criteria

1) Patients who have serious visceral disease or have early history of the disease.
2) Patients who are pregnant, suspected to be pregnant or breastfeeding.
3) Patients who have early history of serious side-effects or allergy to thallium-201.
4) Patients who are considered not to be eligible by the investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation of olfactory nerve with Olfacto-scintigraphy 24 hrs after the nasal administration of thallium-201.
Secondary Outcome Measures
NameTimeMethod
Safety for the nasal administration of thallium-201 in patients with olfactory dysfunction
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