A study on the dermatological efficacy of lotion (BSL05-161025E)

A study on the dermatological efficacy of lotion (BSL05-161025E) - A study on the dermatological efficacy of lotion (BSL05-161025E)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000025455

Enrollment

Registered

2017-01-10

Start date

2017-01-18

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 test lotion and the placebo lotion on one half of the face and the other side, respectively, twice a day for 8 weeks.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Healthy Japanese females with wrinkle grading score from 2.75 to 3.25

Exclusion criteria

Exclusion criteria: -Subjects with sensitive skin or allergy against facial cleanser or cosmetic products -Subjects with skin diseases such as atopic dermatitis, psoriasis and severe acne -Subjects with pollen allergy -Subjects seemed inappropriate to participate in this study by the principle investigator -Subjects who have medical treatment or take some medicine for their facial skin

Design outcomes

Primary

Measure	Time frame
Evaluation of dermatological assessment, wrinkle assessment, skin water content, transepidermal water loss and skin elasticity before and after the repeated treatment for 4 and 8 weeks with the lotions.	—

Countries

Japan

Contacts

Public ContactYoko Endo

Kao Corporation R&D -Core Technology- Biological Science Research

endou.youko1@kao.co.jp0465-34-6116

Outcome results

None listed

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