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Comparison of Olfactory Training in Olfactory Impaired Cases with Unknown Cause

Comparative Study of Olfactory Training in Patients with Idiopathic Olfactory Dysfunction

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs041250213
Enrollment
60
Registered
2026-03-24
Start date
2026-03-24
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic olfactory dysfunction Idiopathic olfactory dysfunction

Interventions

Study participants will be randomly assigned to either the soup food group or the olfactory training kit group at the time of enrollment. Participants in the soup food group will take the soup food on
D000094562

Sponsors

Shiga Hideaki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Idiopathic olfactory dysfunction. 2) No apparent cause in medical history, such as common cold (including COVID-19), head trauma, or dementia. 3) No abnormal findings in the nasal sinuses on nasal fiberoptic or sinus CT. 4) No significant intracranial cerebral atrophy, cerebrovascular disease, or brain tumor on head MRI. 5) Average of odor recognition threshold in T&T olfactometry of 2.6 to 4.0 (moderately depressed) or 4.2 to 5.4 (severely depressed). 6) Age is 50 years or older. 7) Gender is unspecified. 8) Outpatients. 9) Independent in daily activities. 10) Written informed consent has been obtained from the patient, freely given after a sufficient explanation of the study and before participation.

Exclusion criteria

Exclusion criteria: 1) Patients with olfactory dysfunction for more than 3 years. 2) Patients who received olfactory stimulation therapy within 1 month prior to the start of the study. 3) Patients taking oral steroids, nasal steroids, zinc preparations, vitamin B12 preparations or Chinese herbal preparations. 4) Patients with a threshold value exceeding 8 dB in either the right or left tympanic nerve area in an electrical taste test. 5) Patients with a history of airway hypersensitivity disease such as poorly controlled asthma. 6) Patients with a history of food allergy, or with a positive test result for allergens that cause food allergy in allergy test View 39. 7) Patients suffering from or with a history of serious internal organ diseases. 8) Patients who are deemed inappropriate as study participants by the principal investigator or a physician in charge of the research.

Design outcomes

Primary

MeasureTime frame
Average of odor recognition threshold in T&T olfactometry

Secondary

MeasureTime frame
Number of correct answers to the card-based olfactory identification ability test (Open Essence), results of the daily smell questionnaire, questionnaires on diet and health status, olfactory stimulus/meal record card, and percentage of adverse event occurrence.

Contacts

Public ContactHideaki Shiga

Kanazawa Medical University

shigah@kanazawa-med.ac.jp+81-76-218-8147

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026