Unique ID issued by UMIN | UMIN000028982 |
---|---|
Receipt number | R000033163 |
Scientific Title | A confirmation study of the effect on human basal metabolism by consumption of the food which contains plant extract |
Date of disclosure of the study information | 2017/09/06 |
Last modified on | 2020/10/06 09:57:10 |
A confirmation study of the effect on human basal metabolism by consumption of the food which contains plant extract
An effect study of plant extract on human basal metabolism
A confirmation study of the effect on human basal metabolism by consumption of the food which contains plant extract
An effect study of plant extract on human basal metabolism
Japan |
Healthy male adult
Not applicable | Adult |
Others
NO
To confirm the effect of consumption of the food that contains plant extract on human basal metabolism.
Efficacy
Basal metabolic rate
*Heart rate
*Deep body temperature
*Sleep situation
Interventional
Cross-over
Randomized
Individual
Double blind -all involved are blinded
Placebo
2
Prevention
Food |
Test food consumption, 5 weeks for efficiency evaluation, within 7 weeks for safety evaluation.-Washout 5 to 12 weeks-Control food consumption, 5 weeks for efficiency evaluation, within 7 weeks for safety evaluation.-
Control food consumption, 5 weeks for efficiency evaluation, within 7 weeks for safety evaluation.--Washout 5 to 12 weeks-Test food consumption, 5 weeks for efficiency evaluation, within 7 weeks for safety evaluation.-
20 | years-old | <= |
49 | years-old | >= |
Male
1)Healthy males aged 20 to 49 years old.
2)Subjects whose body mass index (BMI) is 19.0 kg/m2 to 29.9kg/m2
3)Subjects whose visceral fat area is less than 100cm2
4)Subjects who have constant life cycle and custom to go to bed until around 1 a.m.
5)Subjects giving written informed consent.
1)Subjects who have severe disease in liver, kidney, heart, lung, digestive organ, blood, endocrine system and metabolic system.
2)Subjects who are receiving treatment or medication at the giving point of informed consent.
3)Subjects who have a history of allergic reaction or hypersensitivity to drug medicine and food.
4)Subjects who have a smoking habit.
5)Subjects who drink alcohol a lot.
6)Subjects who have midnight work or irregular shift work.
7)Subjects who cannot stay and lodging in the facility four times.
8)Subjects who are concerned about rashes and itching by attaching electrode pad.
9)Subjects who have no response in power spectrum of heart rate variability after stimulation of autonomic nerve system.
10)Subjects who are participating in the other clinical tests. Subjects who participated within 1 month prior to the current study and/or who plan to participate in the other clinical tests.
11)Subjects who have been judged as unsuitable for the study by the principal investigator or sub-investigator.
40
1st name | Takayuki |
Middle name | |
Last name | Kodama |
MORISHITA JINTAN CO.,LTD.
Health Care Product Department
540-0004
2-40, Tamatsukuri 1-Chome, Chuo-Ku, Osaka-city, Osaka
072-800-1044
t-kodama@jintan.co.jp
1st name | Makoto |
Middle name | |
Last name | Ichinohe |
CPCC Company Limited
Plan Sales Department
101-0047
4F Chusin Building, 3-3-5 Uchikanda Chiyoda-ku, Tokyo 101-0047, JAPAN
03-5297-3112
cpcc-contact@cpcc.co.jp
CPCC Company Limited
MORISHITA JINTAN CO.,LTD.
Profit organization
Institutional Review Board of Chiyoda Paramedical Care Clinic
2F Chushin Building, 3-3-5 Uchikanda Chiyoda-ku, Tokyo 101-0047, Japan
03-5297-5548
IRB@cpcc.co.jp
NO
2017 | Year | 09 | Month | 06 | Day |
Unpublished
Completed
2017 | Year | 08 | Month | 17 | Day |
2017 | Year | 09 | Month | 07 | Day |
2017 | Year | 09 | Month | 04 | Day |
2020 | Year | 10 | Month | 06 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000033163