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A Study on skin improving effects of a pseudo-ceramide containing formulation

A Study on skin improving effects of a pseudo-ceramide containing formulation - Evaluation of a pseudo-ceramide containing formulation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000035170
Enrollment
60
Registered
2019-02-07
Start date
2019-02-07
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Apply the model water based lotion and model lotion on facial skin for twice a day for a week. And apply the pseudo-ceramide containing formulation and model lotion on facial skin for twice a day f
skin for twice a day for 4 weeks. Apply the model water based lotion and model lotion on facial skin for twice a day for a week. And apply the water based lotion on the market and model lotion on fac
skin for twice a day for 4 weeks.

Sponsors

Kao Corporation
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Healthy female aged from 20 to 49 years old. 2.Subjects who have sensitive and dry skin consciousness. 3.Subjects who can agree to participate in the study voluntarily in writing. 4.Subjects who can agree to change her currently-using cosmetics to designated ones during the test period.

Exclusion criteria

Exclusion criteria: 1.Subjects who has abnormalities in the skin of the measurement regions 2.Subjects who regularly goes to hospital. 3.Subjects with the anamnesis of an alcohol or a drug dependence. 4.Subjects who regularly use drugs (hypnotic drug, anti-allergic drug, analgetic drug, hormonal drug, laxative, antiflatulent etc...). 5.Subjects who has possibilities for emerging allergy to cosmetics and/or foods (including experiences of skin irritation by cosmetics within a year). 6.Subjects who has allergy to adhesive tape and/or medical tape. 7.Subjects who suffers pollen allergy, severe rhinitis and atopic dermatitis. 8.Subjects who is pregnant or lactating, or planned to become pregnant during a test period. 9.Subjects who participates in the other clinical studies within 4 weeks in the past, or person who scheduled to participate in other clinical studies during the test period. 10.Subjects who is judged as unsuitable for the study by the investigator for other reasons. 11.Subjects who herself and/or her family members are working for the cosmetics company, the food company, an advertising agency, investigation and consultant business, and a mass media-related company. 12.Person who experienced medical cosmetic treatments (i.e. cosmetic surgery, collagen injection etc..)

Design outcomes

Primary

MeasureTime frame
Evaluation of the transepidermal water loss,after treatments for 4 weeks use with the pseudo-ceramide containing formulation

Secondary

MeasureTime frame
Evaluation of the stratum corneum water content,transepidermal water loss,sebum secretion,skin color,skin viscoelasticity,stratum corneum,dermatological assessment,a questionnaire survey and VAS after treatments for 4 weeks use with the pseudo-ceramide containing formulation

Countries

Japan

Contacts

Public ContactDaisuke Watanabe

Kao Corporation R&D Skin Care Products Research

watanabe.daisuke2@kao.com0465-34-0559

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026