| Unique ID issued by UMIN | UMIN000055785 |
|---|---|
| Receipt number | R000063742 |
| Scientific Title | Evaluation of the effects of foods containing olive leaf extract powder for skin |
| Date of disclosure of the study information | 2024/10/08 |
| Last modified on | 2024/10/21 13:42:25 |
Evaluation of the effects of foods containing olive leaf extract powder for skin
Evaluation of the effects of foods containing olive leaf extract powder for skin
Evaluation of the effects of foods containing olive leaf extract powder for skin
Evaluation of the effects of foods containing olive leaf extract powder for skin
| Japan |
Not applicable
| Not applicable | Adult |
Others
NO
To verify the effects on skin based on skin texture, wrinkles, brightness, the age of skin, and blood vessel age after consumption for 12 weeks of olive leaf extract powder.
Safety,Efficacy
VISIA score
(1) Transedermal water loss (TEWL)
(2) Water content
(3) Blood vessel age
Interventional
Parallel
Randomized
Individual
Double blind -all involved are blinded
Placebo
2
Prevention
| Food |
Daily intake of test food for 12 weeks
Daily intake of placebo (control food) for 12 weeks
| 40 | years-old | <= |
| 69 | years-old | >= |
Male and Female
1) Healthy Japanese men and women between the ages of 40 and 69 at the time of consent.
2) Persons who feel that their skin is aging but are not taking active anti-aging care.
3) Persons who have been fully informed of the purpose and content of the study, and submit the written informed consent form
1)Persons who are on treatment for a serious illness.
2) Persons with or treating skin disease.
3) Persons who can be expected to have hay fever during the study.
4) Persons who had procedures that may affect the study.
5) Persons with food allergies or those who may be allergic to the test food.
6) Persons who regularly use licensed drugs or quasi-drugs that may affect the study.
7) Persons who regularly use health foods that may affect the study.
8) Persons who are participating in a clinical trial or have participated in another clinical trial within 1 months from the date of obtaining consent.
9) Persons with excessive sunburn.
10) Persons who intentionally cannot refrain from exposure to direct sunlight during the study.
11) Persons who are smokers or who are currently nonsmokers but have smoked within 3 months prior to the start of the study.
12) Persons who receive skin care treatments or use beauty devices daily.
13) Persons who have experience in cosmetic surgery.
14) Persons who have tattoos, surgical scars, or other scars on the measurement area (face or forearms)
15) Persons unable to maintain daily routines.
16) Persons who are on pregnant, lactating, or wishing to become pregnant.
17) Persons who plan to participate in other examinations during the study.
18) Persons who are deemed inappropriate for this study by the investigator.
50
| 1st name | Marie |
| Middle name | |
| Last name | Hayashida |
Nutrition Act Co.,Ltd.
Planning Sect
104-0061
3F Office floor, Daiwa Royal Ginza Bldg. 1-13-15 Ginza, Chuo-ku, Tokyo 104-0061 JAPAN
03-3538-5811
m-hayashida@n-act.co.jp
| 1st name | Masako |
| Middle name | |
| Last name | Mizuuchi |
APO PLUS STATION CO., LTD.
Clinical Operations Dept., CRO Business div.
103-0027
2-14-1, Nihonbashi, Chuo-ku, Tokyo, 103-0027, Japan
03-6777-7789
food-contact@apoplus.co.jp
APO PLUS STATION CO., LTD.
Nutrition Act Co.,Ltd.
Profit organization
Ethics Review Committee of Watanabe Hospital
1-5-16, Haneda, Otaku, Tokyo, 144-0043, Japan
03-3741-0223
food-contact@apoplus.co.jp
NO
医療法人社団 渡辺病院(東京都)
| 2024 | Year | 10 | Month | 08 | Day |
Unpublished
No longer recruiting
| 2024 | Year | 10 | Month | 04 | Day |
| 2003 | Year | 10 | Month | 08 | Day |
| 2024 | Year | 10 | Month | 09 | Day |
| 2025 | Year | 02 | Month | 28 | Day |
| 2024 | Year | 10 | Month | 08 | Day |
| 2024 | Year | 10 | Month | 21 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063742