UMIN-CTR Clinical Trial

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

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Basic information

Public title

Evaluation of the effects of foods containing olive leaf extract powder for skin

Acronym

Evaluation of the effects of foods containing olive leaf extract powder for skin

Scientific Title

Evaluation of the effects of foods containing olive leaf extract powder for skin

Scientific Title:Acronym

Evaluation of the effects of foods containing olive leaf extract powder for skin

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

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.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

VISIA score

Key secondary outcomes

(1) Transedermal water loss (TEWL)
(2) Water content
(3) Blood vessel age


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Daily intake of test food for 12 weeks

Interventions/Control_2

Daily intake of placebo (control food) for 12 weeks

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

40 years-old <=

Age-upper limit

69 years-old >=

Gender

Male and Female

Key inclusion criteria

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

Key exclusion criteria

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.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Marie
Middle name
Last name Hayashida

Organization

Nutrition Act Co.,Ltd.

Division name

Planning Sect

Zip code

104-0061

Address

3F Office floor, Daiwa Royal Ginza Bldg. 1-13-15 Ginza, Chuo-ku, Tokyo 104-0061 JAPAN

TEL

03-3538-5811

Email

m-hayashida@n-act.co.jp


Public contact

Name of contact person

1st name Masako
Middle name
Last name Mizuuchi

Organization

APO PLUS STATION CO., LTD.

Division name

Clinical Operations Dept., CRO Business div.

Zip code

103-0027

Address

2-14-1, Nihonbashi, Chuo-ku, Tokyo, 103-0027, Japan

TEL

03-6777-7789

Homepage URL


Email

food-contact@apoplus.co.jp


Sponsor or person

Institute

APO PLUS STATION CO., LTD.

Institute

Department

Personal name



Funding Source

Organization

Nutrition Act Co.,Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics Review Committee of Watanabe Hospital

Address

1-5-16, Haneda, Otaku, Tokyo, 144-0043, Japan

Tel

03-3741-0223

Email

food-contact@apoplus.co.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

医療法人社団 渡辺病院(東京都)


Other administrative information

Date of disclosure of the study information

2024 Year 10 Month 08 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


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



Progress

Recruitment status

No longer recruiting

Date of protocol fixation

2024 Year 10 Month 04 Day

Date of IRB

2003 Year 10 Month 08 Day

Anticipated trial start date

2024 Year 10 Month 09 Day

Last follow-up date

2025 Year 02 Month 28 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2024 Year 10 Month 08 Day

Last modified on

2024 Year 10 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063742