Unique ID issued by UMIN | UMIN000054004 |
---|---|
Receipt number | R000061653 |
Scientific Title | Excessive Intake Safety Test of the Research Food -Single Arm Open Label Trial- |
Date of disclosure of the study information | 2024/04/09 |
Last modified on | 2024/08/01 10:40:07 |
Excessive Intake Safety Test of the Research Food
-Single Arm Open Label Trial-
Excessive Intake Safety Test of the Research Food
-Single Arm Open Label Trial-
Excessive Intake Safety Test of the Research Food
-Single Arm Open Label Trial-
Excessive Intake Safety Test of the Research Food
-Single Arm Open Label Trial-
Japan |
Healthy adults
Adult |
Others
NO
To examine the safety of the research food by having males and females aged 20 to under 65 consume five times the daily recommended intake of the research food consistently for four weeks.
Safety
-Physical examination (weight, BMI, blood pressure, pulse)
-Blood test items (hematological examination, biochemical blood test)
-Urinalysis
-Incidence of adverse events and side effects
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Prevention
Food |
Participants are to take, without chewing, four tablets of the research food after breakfast once a day for four weeks.
20 | years-old | <= |
65 | years-old | > |
Male and Female
1.Age: 20 to less than 65 years
2.Japanese males and females
3.Individuals with a BMI of less than 30.0kg/m^2
4.Capable of entering data via a smartphone or PC electronic diary
5.Individuals who have received adequate explanation regarding the trial, can comprehend its contents, and have produced written consent
1.Currently undergoing pharmacological treatment (except for on-demand medicines)
2.Currently under dietary or exercise therapy supervised by a physician
3.Individuals with a current or past history of serious disease
4.Those aware of their propensity to develop diarrhea
5.Individuals with surgical history on the digestive tract (appendicitis is acceptable)
6.Individuals with current or past food or drug allergies
7.Habitual heavy drinkers (benchmark: daily pure alcohol consumption exceeding 40g)
8.Heavy smokers (benchmark: over 21 cigarettes per day)
9.Individuals who work night shifts in rotating shifts
10.Those planning major lifestyle changes (diet, sleep, exercise habits, etc.) during the test period, such as long trips
11.Currently pregnant or breastfeeding individuals, or those hoping to get pregnant during the trial period
12.Past occurrences of vasovagal reaction or felt unwell immediately after blood collection
13.Participants in other clinical trials of drugs or health foods, within four weeks post-trial, or planning to participate in other clinical trials after consent to participate in this trial
14.Those who performed blood donation or plasma donation within three months before the start of the trial
15.Individuals deemed unsuitable for the trial by the principal investigator or co-principal investigator
12
1st name | Shun |
Middle name | |
Last name | Schikula |
KINS Co,.Ltd.
Research and Development Team Manager
152-0021
1-33-6-206, Ebisunishi, Shibuya-ku, Tokyo
03-4580-2285
schikula_shun@yourkins.com
1st name | Yoshitada |
Middle name | |
Last name | Hira |
IMEQRD Co., Ltd.
Planning and Sales Department
104-0061
6-2-1 Ginza Chuo-ku Tokyo Japan
03-6704-5968
https://imeqrd.co.jp/
clinical-trial@imeqrd.co.jp
IMEQRD Co. Ltd.
KINS Co,.Ltd.
Profit organization
Suda Clinic institutional review board
2-8-14,Takadanobaba,Shinjyuku,Tokyo
03-6704-5968
jimukyoku@imeqrd.co.jp
NO
2024 | Year | 04 | Month | 09 | Day |
Unpublished
Completed
2024 | Year | 03 | Month | 04 | Day |
2024 | Year | 03 | Month | 26 | Day |
2024 | Year | 04 | Month | 10 | Day |
2024 | Year | 06 | Month | 11 | Day |
2024 | Year | 03 | Month | 29 | Day |
2024 | Year | 08 | Month | 01 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000061653