UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000035133 |
|---|---|
| Receipt number | R000040047 |
| Scientific Title | Exploratory clinical study on sensory evaluation of salty taste and umami mixed aqueous solution. |
| Date of disclosure of the study information | 2018/12/12 |
| Last modified on | 2023/12/22 16:51:08 |
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Basic information
Public title
Exploratory clinical study on sensory evaluation of salty taste and umami mixed aqueous solution.
Acronym
Exploratory clinical study on sensory evaluation of salty taste and umami mixed aqueous solution.
Scientific Title
Exploratory clinical study on sensory evaluation of salty taste and umami mixed aqueous solution.
Scientific Title:Acronym
Exploratory clinical study on sensory evaluation of salty taste and umami mixed aqueous solution.
Region
| Japan |
Condition
Condition
adults
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Study the interaction of salty taste and umami mixed aqueous solution on taste.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Exploratory
Trial characteristics_2
Explanatory
Developmental phase
Not applicable
Assessment
Primary outcomes
Taste (salty taste, umami, palatability etc.)
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Non-randomized
Randomization unit
Blinding
Open -but assessor(s) are blinded
Control
Dose comparison
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
6
Purpose of intervention
Prevention
Type of intervention
| Food |
Interventions/Control_1
0.1 % MSG + 0.1-0.9 % NaCl aqueous solution (w / v)
Interventions/Control_2
0.2 % MSG + 0.1-0.9 % NaCl aqueous solution (w / v)
Interventions/Control_3
0.3 % MSG + 0.1-0.9 % NaCl aqueous solution (w / v)
Interventions/Control_4
0.4 % MSG + 0.1-0.9 % NaCl aqueous solution (w / v)
Interventions/Control_5
0.5 % MSG + 0.1-0.9 % NaCl aqueous solution (w / v)
Interventions/Control_6
0.6 % MSG + 0.1-0.9 % NaCl aqueous solution (w / v)
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 20 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Female
Key inclusion criteria
Adult men and women who agreed to participate in this research with written informed consent.
Key exclusion criteria
(1) Persons with eating disorders.
(2) Persons with taste disorders.
(3) Persons who has eaten within 2 hours.
(4) Persons who judged that a principal investigator is inappropriate for participating in the examination.
Target sample size
12
Research contact person
Name of lead principal investigator
| 1st name | Hitomi |
| Middle name | |
| Last name | Hayabuchi |
Organization
Fukuoka Women's University
Division name
Department of Food and Health Sciences, International College of Arts and Sciences
Zip code
813-8529
Address
1-1-1 Kasumigaoka, Higashiku, Fukuoka, Japan
TEL
092-661-2411
s-hayabuchi@fwu.ac.jp
Public contact
Name of contact person
| 1st name | Kiyoshi |
| Middle name | |
| Last name | Koga |
Organization
Fukuoka Women's University
Division name
General Affairs Management Group
Zip code
813-8529
Address
1-1-1 Kasumigaoka, Higashiku, Fukuoka, Japan
TEL
092-661-2411
Homepage URL
keiei@fwu.ac.jp
Sponsor or person
Institute
Fukuoka Women's University
Institute
Department
Personal name
Funding Source
Organization
Fukuoka Women's University
Organization
Division
Category of Funding Organization
Local Government
Nationality of Funding Organization
Other related organizations
Co-sponsor
Ajinomoto co., Inc.
Name of secondary funder(s)
Ajinomoto co., Inc.
IRB Contact (For public release)
Organization
Research Ethics Review Committee at Fukuoka Women's University
Address
Kasumigaoka, Higashiku, Fukuoka, Japan
Tel
092-661-2411
keiei@fwu.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
福岡女子大学 / Fukuoka Women’s University
Other administrative information
Date of disclosure of the study information
| 2018 | Year | 12 | Month | 12 | 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
Main results already published
Date of protocol fixation
| 2016 | Year | 06 | Month | 22 | Day |
Date of IRB
| 2016 | Year | 06 | Month | 22 | Day |
Anticipated trial start date
| 2016 | Year | 07 | Month | 01 | Day |
Last follow-up date
| 2016 | Year | 10 | Month | 07 | Day |
Date of closure to data entry
| 2016 | Year | 10 | Month | 12 | Day |
Date trial data considered complete
| 2019 | Year | 05 | Month | 16 | Day |
Date analysis concluded
| 2019 | Year | 09 | Month | 30 | Day |
Other
Other related information
Management information
Registered date
| 2018 | Year | 12 | Month | 04 | Day |
Last modified on
| 2023 | Year | 12 | Month | 22 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000040047
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| Registered date | File name |
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