UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000059853 |
|---|---|
| Receipt number | R000068444 |
| Scientific Title | A study on blood beta-carotene kinetics after consumption of the test food: a randomized, double-blind, active-controlled, crossover comparison study |
| Date of disclosure of the study information | 2025/11/21 |
| Last modified on | 2025/11/21 15:35:06 |
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Basic information
Public title
A study on blood beta-carotene kinetics after consumption of the test food: a randomized, double-blind, active-controlled, crossover comparison study
Acronym
A study on blood beta-carotene kinetics after consumption of the test food: a randomized, double-blind, active-controlled, crossover comparison study
Scientific Title
A study on blood beta-carotene kinetics after consumption of the test food: a randomized, double-blind, active-controlled, crossover comparison study
Scientific Title:Acronym
A study on blood beta-carotene kinetics after consumption of the test food
Region
| Japan |
Condition
Condition
Healthy Japanese
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To observe blood beta-carotene kinetics after oral consumption of green juice products manufactured by different processes.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Pragmatic
Developmental phase
Not applicable
Assessment
Primary outcomes
1. Change in blood beta-carotene level from before the intervention to three hours after the intervention
Key secondary outcomes
1. Measured value of blood beta-carotene level before the intervention and three hours after the intervention
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Double blind -all involved are blinded
Control
Active
Stratification
Dynamic allocation
Institution consideration
Institution is not considered as adjustment factor.
Blocking
YES
Concealment
Central registration
Intervention
No. of arms
2
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Food |
Interventions/Control_1
<Duration>
Two single ingestions
<Test products>
Screening: Green juice powder B
Test 1: Green juice powder A
Test 2: Green juice powder B
<Administration>
Dissolve two packets (8 g) in 200 mL of water and consume.
*Test 1 followed by Test 2.
*The washout period is one week or more.
Interventions/Control_2
<Duration>
Two single ingestions
<Test products>
Screening: Green juice powder B
Test 1: Green juice powder B
Test 2: Green juice powder A
<Administration>
Dissolve two packets (8 g) in 200 mL of water and consume.
*Test 1 followed by Test 2.
*The washout period is one week or more.
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. Japanese
2. Men or women
3. Adults
4. Healthy individuals
5. Individuals whose BMI is < 30 kg/m2 at screening
6. Individuals whose blood beta-carotene level three hours after the consumption of the control product at screening is higher than before consumption
Key exclusion criteria
1. Individuals who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, or myocardial infarction
2. Individuals who have a pacemaker or an implantable cardioverter defibrillator (ICD)
3. Individuals who are currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, chronic kidney disease, cerebrovascular disorder, rheumatic disease, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases
4. Individuals who are taking "Foods for Specified Health Uses" or "Foods with Functional Claims"
5. Individuals who are taking or using medicines (including herbal medicines) or supplements, particularly those who regularly take beta-carotene, vitamin A, or multivitamins
6. Individuals who are allergic to medicines or foods related to the test product, particularly wheat, milk, beef, soy, chicken, banana, pork, or apple
7. Individuals who regularly consume vegetables, fruits, yogurt, or other similar foods
8. Individuals who regularly consume alcohol in excess (averaging more than about 20 g of pure alcohol per day) {e.g., 500 mL: a medium bottle of beer or about 1.5 cans of canned chu-hi, 180 mL: 1 go of sake or about 1.5 glasses of wine, 90 mL: half-go with shochu, 60 mL: a glass of whiskey brandy (double)}
9. Individuals who are pregnant, lactating, or planning to become pregnant during this study
10. Individuals who have been enrolled in other clinical studies within the last 28 days before the agreement to participate in this study or plan to participate in another study during this study
11. Individuals who are judged as ineligible to participate in this study by the physician
Target sample size
12
Research contact person
Name of lead principal investigator
| 1st name | Tsuyoshi |
| Middle name | |
| Last name | Takara |
Organization
Medical Corporation Seishinkai, Takara Clinic
Division name
Director
Zip code
141-0022
Address
9F Taisei Bldg., 2-3-2, Higashi-gotanda, Shinagawa-ku, Tokyo, Japan
TEL
03-5793-3623
t-takara@takara-clinic.com
Public contact
Name of contact person
| 1st name | Naoko |
| Middle name | |
| Last name | Suzuki |
Organization
ORTHOMEDICO Inc.
Division name
R&D Department
Zip code
112-0002
Address
2F Sumitomo Fudosan Korakuen Bldg., 1-4-1, Koishikawa, Bunkyo-ku, Tokyo, Japan
TEL
03-3818-0610
Homepage URL
nao@orthomedico.jp
Sponsor or person
Institute
Yakult Health Foods Co., Ltd.
Institute
Department
Personal name
Funding Source
Organization
Yakult Health Foods Co., Ltd.
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
The ethical committee of the Takara Clinic, Medical Corporation Seishinkai
Address
9F Taisei Bldg., 2-3-2, Higashi-gotanda, Shinagawa-ku, Tokyo, Japan
Tel
03-5793-3623
IRB@takara-clinic.com
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
医療法人社団盛心会 タカラクリニック (東京都)
Medical Corporation Seishinkai, Takara Clinic (Tokyo, Japan)
南町医院 (東京都)
Nerima Medical Association, Minami-machi Clinic (Tokyo, Japan)
Other administrative information
Date of disclosure of the study information
| 2025 | Year | 11 | Month | 21 | 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
Open public recruiting
Date of protocol fixation
| 2025 | Year | 11 | Month | 12 | Day |
Date of IRB
| 2025 | Year | 11 | Month | 12 | Day |
Anticipated trial start date
| 2025 | Year | 11 | Month | 21 | Day |
Last follow-up date
| 2026 | Year | 03 | Month | 01 | 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 | 11 | Month | 21 | Day |
Last modified on
| 2025 | Year | 11 | Month | 21 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000068444
