Unique ID issued by UMIN | UMIN000023050 |
---|---|
Receipt number | R000026568 |
Scientific Title | A study for safety evaluation of excess consumption of the test drink. |
Date of disclosure of the study information | 2016/07/07 |
Last modified on | 2020/10/05 13:31:52 |
A study for safety evaluation of excess consumption of the test drink.
Safety evaluation of excess consumption of the test drink.
A study for safety evaluation of excess consumption of the test drink.
Safety evaluation of excess consumption of the test drink.
Japan |
Healthy adult
Not applicable | Adult |
Others
NO
Safety evaluation of excess consumption of the test drink in 4 consecutive weeks.
Safety
The incidence of side effects and adverse events.
Blood test
Urine test
Blood pressure/pulsation
Weight/body mass index
Medical interview
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Food |
The drink which contains indigestible dextrin. Intake 4-weeks.
20 | years-old | <= |
70 | years-old | > |
Male and Female
(1)Healthy adults aged 20 to 69years old.
(2)Subjects giving written informed consent.
(1)Subjects who are given continuous treatment by taking medicines.
(2) Subjects who constantly use oral medicines, functional foods and/or supplements having a possibility of affecting test results.
(3)Subjects who have previous and/or current medical history of serious disease (e.g., heart, liver, kidney, digestive organ).
(4) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period.
(5)Subjects who excessive alcohol intake.
(6) Subjects who have extremely irregular dining habits, and subjects who have midnight work or irregular shift work.
(7)Subjects who have previous medical history of drug and/or food allergy.
(8) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests.
(9)Subjects who donated over 200mL blood and/or blood components within the last one month to the current study.
(10) Subjects who donated over 400mL blood and/or blood components within the last three month to the current study.
(11) Females who donated over 400mL blood and/or blood components within the last four month to the current study.
(12) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study.
(13) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study.
(14)Others who have been determined ineligible by principal investigator or sub-investigator.
33
1st name | Suguru |
Middle name | |
Last name | Fujiwara |
CPCC Company Limited
Clinical Research Planning Department
101-0047
4F Chusin Building, 3-3-5 Uchikanda Chiyoda-ku, Tokyo 101-0047, JAPAN
03-5297-3112
s.fujiwara@cpcc.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
m.i@cpcc.co.jp
CPCC Company Limited
DyDo DRINCO, INC.
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
チヨダパラメディカルケアクリニック(東京) Chiyoda Paramedical Care Clinic (Tokyo)
2016 | Year | 07 | Month | 07 | Day |
Unpublished
Completed
2016 | Year | 05 | Month | 19 | Day |
2016 | Year | 07 | Month | 12 | Day |
2016 | Year | 07 | Month | 07 | Day |
2020 | Year | 10 | Month | 05 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026568