UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000051056 |
|---|---|
| Receipt number | R000058198 |
| Scientific Title | Test Study on the effect of food intake on postprandial blood glucose level |
| Date of disclosure of the study information | 2023/05/16 |
| Last modified on | 2023/08/16 15:13:58 |
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Basic information
Public title
Test Study on the effect of food intake on postprandial blood glucose level
Acronym
Test Study on the effect of food intake on postprandial blood glucose level
Scientific Title
Test Study on the effect of food intake on postprandial blood glucose level
Scientific Title:Acronym
Test Study on the effect of food intake on postprandial blood glucose level
Region
| Japan |
Condition
Condition
Healthy subjects
Classification by specialty
| Not applicable |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to determine the effect of a single intake of the test food on blood glucose levels in Japanese males and females aged 20 to 60.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
iAUC of blood glucose
Key secondary outcomes
Cmax of blood glucose
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Double blind -all involved are blinded
Control
Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Prevention
Type of intervention
| Food |
Interventions/Control_1
Single intake of test food
Interventions/Control_2
Single intake of placebo food
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
| 60 | years-old | > |
Gender
Male and Female
Key inclusion criteria
1.Japanese male and female subjects between 20 and 60 years of age at the time of consent.
2.Subjects who have received a full explanation of the purpose and content of the study, have the ability to consent, understand the study well, and have volunteered to participate in the study and have agreed to participate in the study in writing.
Key exclusion criteria
1.Subjects who have or have had diabetic diseases.
2.Subjects who are currently receiving medication or outpatient treatment for some serious disease.
3.Subjects who are currently undergoing exercise or diet therapy under the supervision of a physician.
4.Subjects who may develop allergies to the test food.
5.Subjects who have a current or history of drug dependence or alcohol dependence.
6.Subjects who are hospitalized for mental disorders (depression, etc.) or sleep disorders, or have a history of mental disorders in the past.
7.Subjects who have irregular rhythm of life due to night work or shift work.
8.Subjects who are with extremely irregular eating, sleeping, or other habits.
9.Subjects who have an extremely unbalanced diet.
10.Subjects who have or have had serious diseases such as brain diseases, malignant tumors, immune diseases, diabetes, liver diseases (hepatitis), kidney diseases, heart diseases, etc., thyroid diseases, adrenal diseases, and other metabolic diseases.
11.Subjects whose fasted blood glucose levels are 126 mg/dL or more or HbA1c levels are 6.5% or more.
12.Subject who use health foods and medicines that contain ingredients that affect blood glucose levels.
13.Subjects who have participated in other clinical trials (research) within 3 months retrospectively from the date of obtaining consent, or those who have plans to participate in other clinical trials (research) during the study period.
14.Subjects who have collected more than 200 mL of blood within 1 month or 400 mL within 3 months prior to the date of obtaining consent.
15.Subjects who are currently pregnant or breastfeeding. or who are likely to become so during the study period.
16.Subjects who have difficulty in complying with the recording of various questionnaires.
17.Subjects who are judged to be inappropriate as subjects based on clinical laboratory test values and measured values at the time of SCR.
Target sample size
10
Research contact person
Name of lead principal investigator
| 1st name | Satoshi |
| Middle name | |
| Last name | Fukumitsu |
Organization
NIPPN CORPORATION
Division name
Central Laboratory Innovation Center
Zip code
243-0041
Address
5-1-3, Midorigaoka, Atsugi, Kanagawa, Japan
TEL
046-222-6963
sfukumitsu@nippn.co.jp
Public contact
Name of contact person
| 1st name | Masao |
| Middle name | |
| Last name | Matsuoka |
Organization
M&I Science CORP.
Division name
Clinical Development Department
Zip code
531-0071
Address
NAKATSUGRAND Bld.10F, 1-17-26, Nakatsu, Kita-ku, Osaka-Shi, Osaka, Japan
TEL
06-7878-6780
Homepage URL
m.matsuoka@mis21.co.jp
Sponsor or person
Institute
others
Institute
Department
Personal name
Funding Source
Organization
others
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
NISHI-UMEDA Clinic for Asian Medical Collaboration Ethics Review Committee
Address
Maruit Nishi-Umeda Building 3F, 3-3-45 Umeda, Kita-ku, Osaka-shi, Osaka, Japan
Tel
06-4797-5660
jimukyoku@amc-clinc.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
| 2023 | Year | 05 | Month | 16 | 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
Completed
Date of protocol fixation
| 2023 | Year | 03 | Month | 31 | Day |
Date of IRB
| 2023 | Year | 04 | Month | 20 | Day |
Anticipated trial start date
| 2023 | Year | 05 | Month | 17 | Day |
Last follow-up date
| 2023 | Year | 06 | Month | 14 | Day |
Date of closure to data entry
| 2023 | Year | 06 | Month | 23 | Day |
Date trial data considered complete
| 2023 | Year | 06 | Month | 26 | Day |
Date analysis concluded
| 2023 | Year | 07 | Month | 04 | Day |
Other
Other related information
(Exclusion criteria continued)
18.Other subjects who are judged unsuitable as subjects by the principal investigator.
Management information
Registered date
| 2023 | Year | 05 | Month | 15 | Day |
Last modified on
| 2023 | Year | 08 | Month | 16 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000058198
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
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| Registered date | File name |
| Research case data | |
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| Registered date | File name |
