UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000059901
Receipt number R000068503
Scientific Title Anti-wrinkle evaluation test using test substance combination preparations
Date of disclosure of the study information 2025/11/28
Last modified on 2025/11/27 15:22:54

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Basic information

Public title

Anti-wrinkle evaluation test using test substance combination preparations

Acronym

Anti-wrinkle evaluation test using test substance combination preparations

Scientific Title

Anti-wrinkle evaluation test using test substance combination preparations

Scientific Title:Acronym

Anti-wrinkle evaluation test using test substance combination preparations

Region

Japan


Condition

Condition

Healthy adult female

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the anti-wrinkle effect of the test product.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

(1) Wrinkle grade on the outer corner of the eyes by visual and photographic evaluation
(2) Wrinkle area percentage, total average depth of wrinkles, average depth of maximum wrinkles, and maximum depth of maximum wrinkles on the corner of the eyes using replica

Key secondary outcomes

(1) Stratum corneum water content (2) TEWL
(3) Blemishes, wrinkles, pores, color irregularities, porphyrins, hidden spots, melanin index, hemoglobin index by VISIA imaging
Wrinkle grade on the outer corner of the eyes by visual and photographic evaluation
(4) IL-1RA/IL-1 alpha, cell area, degree of multiple exfoliation, carbonylated proteins, and Involucrin/Nile red stain, lipid quantification using tape-stripped stratum corneum
(5) Usability questionnaire


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

6

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

Using the half-face method, apply Test Product 1 to one side of the face for 12 weeks.

Interventions/Control_2

On the opposite side, which received Test Product 1, apply the control product for 12 weeks.

Interventions/Control_3

Using the half-face method, apply Test Product 2 to one side of the face for 12 weeks.

Interventions/Control_4

On the opposite side, which received Test Product 2, apply the control product for 12 weeks.

Interventions/Control_5

Using the half-face method, apply Test Product 3 to one side of the face for 12 weeks.

Interventions/Control_6

On the opposite side, which received Test Product 3, apply the control product for 12 weeks.

Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

40 years-old <=

Age-upper limit

60 years-old >=

Gender

Female

Key inclusion criteria

(1) Age between 40 and 60
(2) Female
(3) Subjects with wrinkles of grade 3 to 5 on the left and right corners of the eyes
(4) Subjects who only use 1-2 items of lotion or milky lotion after washing their face (after bathing)
(5) Subjects who have received a sufficient explanation of the purpose and content of this study, have the ability to consent, and who voluntarily apply for participation after having a good understanding of the study, and who are able to give written consent to participate in this study
(6) Subjects who are aware that there is no difference between the left and right sides of the wrinkles around the eyes and the skin condition of the evaluation area

Key exclusion criteria

1. Subjects who have urticaria, inflammation, eczema, trauma, acne, pimples, warts, blemishes, etc. or their traces on the evaluation site
2. Subjects with a history or current history of atopic dermatitis, or with atopic predisposition
3. Subjects who have received cosmetic treatment at the evaluation site or plan to receive it during the study period
4. Subjects who use creams, gels, all-in-one products, beauty devices, packs or oils on the evaluation site
5. Subjects who continuously use drugs, health foods, supplements, skin care products, cosmetics, quasi-drugs that advocate efficacy related to the efficacy examined in this study
6. Subjects who have performed the following within the past 4 weeks or plan to do so during the study period
a) Changed or started health foods, basic cosmetics or sunscreen agents used on the evaluation sites
b) Exposed to ultraviolet rays beyond daily life
c) Participated in other human trials
d) Received a special skin care treatment on the evaluation site
7. Subjects who work night shifts or day and night shifts
8. Subjects who are undergoing treatment at medical institutions for the treatment or prevention of disease, or those who are judged to require treatment
9. Subjects with a history of serious diseases of sugar metabolism, lipid metabolism, liver function, renal function, heart, circulatory system, respiratory system, endocrine system, immune system, nervous system, alcohol or drug dependence.
10. Subjects who are at risk of developing cosmetic or food allergies
11. Subjects who are pregnant, breastfeeding, or wish to become pregnant during the study period
12. Subjects who are judged by the principal investigator to be unsuitable for study participation
13. Subjects who have significantly different wrinkle grade scores between the left and right corners of the eyes or who are likely to engage in activities that tend to cause side-to-side wrinkles in their daily lives (such as people whose main job is driving a car)

Target sample size

75


Research contact person

Name of lead principal investigator

1st name Wakako
Middle name
Last name Inoue

Organization

YAWARA Dermatology Clinic

Division name

Director

Zip code

530-0041

Address

Sakashin Tenjinbashi Building 4F, 5-7-10 Tenjinbashi, Kita-ku, Osaka City, Osaka, Japan

TEL

06-6882-1130

Email

yawara@koseikai-jp.com


Public contact

Name of contact person

1st name Yuri
Middle name
Last name Okano

Organization

CIEL CO., LTD.

Division name

CIEL CO., LTD.

Zip code

130-0021

Address

Renafine 302, 2-10-11, Midori, Sumida-ku, Tokyo, Japan

TEL

03-6659-2767

Homepage URL


Email

yuri.okano@ciel-tokyo.com


Sponsor or person

Institute

DRC Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

YAMASA CORPORATION

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

Brain Care Clinic Ethics Review Committee

Address

Hakutyo Build. 2F,2-1-2 Shinjuku,Shinjuku-ku,Tokyo

Tel

06-6882-1130

Email

ethics_board@drc-web.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

DRC株式会社(大阪府)


Other administrative information

Date of disclosure of the study information

2025 Year 11 Month 28 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

Preinitiation

Date of protocol fixation

2025 Year 11 Month 12 Day

Date of IRB

2025 Year 11 Month 13 Day

Anticipated trial start date

2025 Year 11 Month 29 Day

Last follow-up date

2026 Year 04 Month 24 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2025 Year 11 Month 27 Day

Last modified on

2025 Year 11 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000068503