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Study of humidity and membrane for skin properties

Study to examine the effect of humidity and formulation membrane on skin properties (2) - Study of humidity and membrane for skin properties

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038552
Enrollment
50
Registered
2019-12-01
Start date
2019-12-01
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

To stay 6 hours a day in each environments (low and middle humidity). To apply the formulation membrane on only the half face for 6 hours during stay in low humidity environment.

Sponsors

Kao Corporation
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Healthy females

Exclusion criteria

Exclusion criteria: 1.Subjects who has become pregnant and breast-feeding or have a possibility of pregnant during the study period. 2.Subjects with illnesses or diseases on their face, especially such as atopic dermatitis, or psoriasis, or severe acne. 3.Subjects who has serious suntan in their faces. 4.Subjects who performs outdoor sport periodically. 5.Subjects who take any OTC or prescription medications, especially anti-inflammation agents, anti-bacterial agents, analgesic agents, hormonal agents, laxative agents, intestinal agents, etc. 6.Subjects who attend the hospital (such as gastrointestinal disease, liver disease, kidney disease, cardiovascular heart disease, skin disease, or poor physical condition). And, panelists for less than one month after attend the hospital. 7.Subjects who has seen in a spa treatment (such as chemical peeling, or laser therapy). And, panelists who has seen in a cosmetic medicine (such as cosmetic surgery, or collagen infusion). 8.Subjects who cannot refrain from facial cleansing on the days of evaluation visits. 9.Subjects who cannot agree with not used mask on the days of evaluation visits. 10.Subjects who are participating or plan to participate in other intervention tests (cosmetics, foods) for facial skin during the test period. 11.Subjects deemed inappropriate to participate in this study by the principle investigator.

Design outcomes

Primary

MeasureTime frame
water content, transepidermal water loss, skin color, surface texture and sebum composition

Countries

Japan

Contacts

Public ContactNaoto Takada

Kao Corporation Biological Science Research

takada.naoto@kao.com0285-68-7231

Outcome results

None listed

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