UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000057760 |
|---|---|
| Receipt number | R000066011 |
| Scientific Title | Evaluation of the Efficacy of Taste Recall Rehabilitation in Individuals with Taste Dysfunction |
| Date of disclosure of the study information | 2025/05/02 |
| Last modified on | 2025/05/09 09:40:43 |
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Basic information
Public title
Evaluation of the Efficacy of Taste Recall Rehabilitation in Individuals with Taste Dysfunction
Acronym
Evaluation of the Efficacy of Taste Recall Rehabilitation in Individuals with Taste Dysfunction
Scientific Title
Evaluation of the Efficacy of Taste Recall Rehabilitation in Individuals with Taste Dysfunction
Scientific Title:Acronym
Evaluation of the Efficacy of Taste Recall Rehabilitation in Individuals with Taste Dysfunction
Region
| Japan |
Condition
Condition
taste dysfunction
Classification by specialty
| Not applicable |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
This study aims to elucidate the effects of taste recall rehabilitation in patients with taste disorders.
Basic objectives2
Safety
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
The effectiveness of taste recall training will be evaluated by comparing taste recognition thresholds before and after a three-day taste recall training program.
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
Taste recall traning
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 18 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
1. Adults aged 18 years or older
2. Patients diagnosed with taste disorders at the Department of Comprehensive Dental Care
3. Individuals who provided written informed consent to participate in the study
Key exclusion criteria
Patients with cognitive impairment indicated by an MMSE score of 23 or lower
Individuals who declined to participate in the study
Individuals with allergies to sucrose, sodium chloride, L(+)-tartaric acid, quinine hydrochloride dihydrate (quinine hydrochloride), hydrochloric acid, or monosodium glutamate
Smokers
Target sample size
28
Research contact person
Name of lead principal investigator
| 1st name | Satoru |
| Middle name | |
| Last name | Ebihara |
Organization
Tohoku University Graduate School of Medicine
Division name
Department of Rehabilitation Medicine
Zip code
980-8575
Address
Seiryo-machi 1-1, Aoba-ku, Sendai
TEL
0227177353
satoru.ebihara.c4@tohoku.ac.jp
Public contact
Name of contact person
| 1st name | Midori |
| Middle name | |
| Last name | Miyagi |
Organization
Tohoku University Graduate School of Medicine
Division name
Department of Rehabilitation Medicine
Zip code
980-8574
Address
Seiryo-machi 1-1, Aoba-ku sendai
TEL
0227177353
Homepage URL
midori.miyagi.b5@tohoku.ac.jp
Sponsor or person
Institute
Tohoku University
Institute
Department
Personal name
Funding Source
Organization
Tohoku University
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Ethics Committee Tohoku University Graduate School of Medicine
Address
2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, 980-8575, Japan
Tel
022-728-4105
ec-med@grp.tohoku.ac.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2025 | Year | 05 | Month | 02 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Preinitiation
Date of protocol fixation
| 2025 | Year | 05 | Month | 02 | Day |
Date of IRB
Anticipated trial start date
| 2025 | Year | 06 | Month | 10 | Day |
Last follow-up date
| 2030 | Year | 06 | Month | 10 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2025 | Year | 05 | Month | 02 | Day |
Last modified on
| 2025 | Year | 05 | Month | 09 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066011
