UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000056549 |
|---|---|
| Receipt number | R000064621 |
| Scientific Title | A test to assess blood glucose responses after intake of baked goods. |
| Date of disclosure of the study information | 2025/01/13 |
| Last modified on | 2024/12/24 11:21:26 |
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Basic information
Public title
A test to assess blood glucose responses after intake of baked goods.
Acronym
A test to assess blood glucose responses after intake of baked goods.
Scientific Title
A test to assess blood glucose responses after intake of baked goods.
Scientific Title:Acronym
A test to assess blood glucose responses after intake of baked goods.
Region
| Japan |
Condition
Condition
Healthy human
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To evaluate the glycemic index (GI) of the test foods.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Glycemic Index (GI)
Key secondary outcomes
Incremental area under the blood glucose response curve (IAUCg)
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Self control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Prevention
Type of intervention
| Food |
Interventions/Control_1
Take the references food in 9 minutes.
<Washout>
Take the references food in 9 minutes.
<Washout>
Take the test food D in 9 minutes.
<Washout>
Take the test food E in 9 minutes.
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
| 20 | years-old | <= |
Age-upper limit
| 50 | years-old | > |
Gender
Male and Female
Key inclusion criteria
1.Fasting plasma glucose level 70 - 110 mg/dL.
2.Individual having screening test result and questionnaire result judged to be appropriate for this study by investigator.
Key exclusion criteria
1.Diabetes mellitus under medical treatment.
2.Individual with a BMI of 30 or higher.
3.Individual with abnormal glucose tolerance in the past year`s testing.
4.Individual taking antipertensive drugs, etc.
5. Individual having sevre diseases (e.g.liver, kidney, heart, blood diseases, and infections requiring the notification)
6.Individual received gastrectomy, enterectomy, and gastro-intestinal diseases, judged to be inappropriate for this study.
7.Pregnant, women having the possibility, and lactating women.
8.Participants in order clinical trial.
9.Individual rejected participating in this study by chief investigator.
Target sample size
16
Research contact person
Name of lead principal investigator
| 1st name | Kenichi |
| Middle name | |
| Last name | Watanabe |
Organization
Niigata Bio-Research Park, Inc
Division name
Advisor
Zip code
956-0841
Address
316-2 Higashijima,Akiha-ku, Niigata City, Niigata, Japan
TEL
0250-25-1196
wataken@med.niigata-u.ac.jp
Public contact
Name of contact person
| 1st name | Hiroshi |
| Middle name | |
| Last name | Goto |
Organization
Niigata Bio Research Park, Inc
Division name
Business Promotion Department
Zip code
950-0841
Address
316-2 Higashijima,Akiha-ku, Niigata City, Niigata, Japan
TEL
0250-25-1196
Homepage URL
goto@nbrp.co.jp
Sponsor or person
Institute
Niigata Bio Research Park, Inc
Institute
Department
Personal name
Funding Source
Organization
Bourbon Corporation
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
NBRC Research Ethics Review Committee
Address
316-2 Higashijima,Akiha-ku, Niigata City, Niigata, Japan
Tel
0250-25-1196
nbrp-food-navi@nbrp.co.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 | 01 | Month | 13 | 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
| 2024 | Year | 11 | Month | 12 | Day |
Date of IRB
Anticipated trial start date
| 2025 | Year | 01 | Month | 13 | Day |
Last follow-up date
| 2025 | Year | 03 | Month | 02 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2024 | Year | 12 | Month | 24 | Day |
Last modified on
| 2024 | Year | 12 | Month | 24 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064621
