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Recruitment status Terminated
Unique ID issued by UMIN UMIN000036590
Receipt No. R000041627
Scientific Title Efficacy test of supplements containing plant extract for Japanese
Date of disclosure of the study information 2020/05/08
Last modified on 2019/05/15

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Basic information
Public title Efficacy test of supplements containing plant extract for Japanese
Acronym Efficacy test of supplements containing plant extract for Japanese
Scientific Title Efficacy test of supplements containing plant extract for Japanese
Scientific Title:Acronym Efficacy test of supplements containing plant extract for Japanese

Condition Healthy Japanese adult
Classification by specialty
Classification by malignancy Others
Genomic information NO

Narrative objectives1 The objective of this study is to verify the effects on body fat of test foods in adult men and women of BMI 25 and under 30 and abdominal visceral fat area (VFA) 80 cm^2.
Basic objectives2 Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Primary outcomes Body fat percentage and change
Neutral fat and change
Key secondary outcomes Weight and change
BMI and change
Waist circumference and change
Hip circumference and amount of change

Study type Interventional

Study design
Basic design Parallel
Randomization Randomized
Randomization unit Individual
Blinding Double blind -all involved are blinded
Control Placebo
Stratification YES
Dynamic allocation
Institution consideration

No. of arms 2
Purpose of intervention Treatment
Type of intervention
Interventions/Control_1 Intake of plant extract-containing food for 12 weeks
Interventions/Control_2 Intake of plant extract free food for 12 weeks

Age-lower limit
20 years-old <=
Age-upper limit
64 years-old >=
Gender Male and Female
Key inclusion criteria 1) Persons aged 20 to 65 years of age at the time of obtaining informed consent
2) A healthy person who is not currently treating any disease
3) Persons with BMI of 25.0 kg / m2 or more and less than 30.0 kg / m2 at screening
4) Persons with a VFA of 80 cm2 or more using a CT scanner system
5) Those who can visit the designated medical institution on the scheduled examination date
6) A person who agreed in writing after fully understanding the purpose and content of this study
Key exclusion criteria 1) Those who have difficulty participating in the study due to liver, kidney, heart disease, respiratory disorder, endocrine disorder, metabolic disorder, neurological disorder, consciousness disorder, diabetes (according to the criteria established by the Japan Diabetes Association), and other diseases.
2) Person with a history of cardiovascular disease
3) Those who are taking glucose metabolism, lipid metabolism, blood pressure improvement drugs
4) Those who regularly use medicines and health foods / supplements (including foods for specified health, functional labeling foods and nutritionally functional foods) that may affect this study (but stop taking it at the time of obtaining consent) The person who can do it does not correspond)
5) Persons who have allergies related to the test food
6) Those who have experienced poor mood or physical condition by blood collection in the past
7) Those who donated more than 200 mL from the month before the start of the test to the start of the test
8) Those who are participating in other clinical trials or within 4 weeks after the trial
9) Alcoholic drinkers and excessive smokers
10) Eating habits are extremely irregular
11) Those who wish to become pregnant during the study period, pregnant women (including those who may be pregnant) or those who are lactating
12) Those who can not agree with the purpose of the description of this exam that is conducted in advance
In addition, those who were judged inappropriate for this study by the study investigator
Target sample size 40

Research contact person
Name of lead principal investigator
1st name Yoshiaki
Middle name
Last name Shiojima
Organization RYUSENDO CO., LTD.
Division name President and CEO
Zip code 171-0021
Address 1-5-3 Nishi-ikebukuro, Toshima-ku, Tokyo 171-0021, Japan
TEL 03-3985-8346

Public contact
Name of contact person
1st name Megumi
Middle name
Last name Takahashi
Organization RYUSENDO CO., LTD.
Division name Development Office
Zip code 171-0021
Address 1-5-3 Nishi-ikebukuro, Toshima-ku, Tokyo 171-0021, Japan
TEL 03-3985-8346
Homepage URL


Funding Source
Organization RYUSENDO CO., LTD.
Category of Funding Organization Profit organization
Nationality of Funding Organization

Other related organizations
Name of secondary funder(s)

IRB Contact (For public release)
Organization Akanuma Surgeon Board Ethics Review Committee
Address Ishiyama 2-jo 6-chome 14-1, Minami-ku, Sapporo-shi, Hokkaido
Tel 011-591-1777

Secondary IDs
Secondary IDs NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2

Institutions 赤沼外科医院(北海道)

Other administrative information
Date of disclosure of the study information
2020 Year 05 Month 08 Day

Related information
URL releasing protocol
Publication of results Unpublished

URL related to results and publications
Number of participants that the trial has enrolled 0
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

Recruitment status Terminated
Date of protocol fixation
2019 Year 03 Month 25 Day
Date of IRB
2019 Year 03 Month 26 Day
Anticipated trial start date
2019 Year 05 Month 20 Day
Last follow-up date
2019 Year 08 Month 31 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other related information

Management information
Registered date
2019 Year 04 Month 24 Day
Last modified on
2019 Year 05 Month 15 Day

Link to view the page

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name

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