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Evaluation of Skin Condition Changes Following Face sheet Mask Use After Cosmetic Medical Procedures

Evaluation of Skin Condition Changes Following Face sheet Mask Use After Cosmetic Medical Procedures - Evaluation of Skin Condition Changes Following Face sheet Mask Use After Cosmetic Medical Procedures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061129
Enrollment
10
Registered
2026-04-02
Start date
2026-04-03
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Adult

Interventions

Participants will apply a facial sheet mask immediately after treatment, followed by seven additional applications over a 28-day period according to a predefined schedule Apply Petrolatum immediately

Sponsors

Shin-Kawasaki Eve Clinic for Dermatology and Aesthetic Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Individuals aged 18 or older at the time of obtaining consent. 2) Individuals who wish to undergo laser treatment. 3) Individuals who have received a full explanation of the purpose and content of the research, have the capacity to give consent, fully understand the information, voluntarily volunteer to participate, and provide written consent to participate in the research.

Exclusion criteria

Exclusion criteria: 1) Individuals whom the principal investigator has determined to have differences in skin condition between the left and right sides of their face. 2) Individuals who plan to undergo cosmetic medical procedures on their face other than those covered by this study during the study period. 3) Individuals at risk of developing an allergic reaction to cosmetics or to ingredients contained in the test products used in this study. 4) Individuals who are pregnant or breastfeeding at the time of consent, or who wish to become pregnant during the study period. 5) Individuals who have participated in another human study within the past four weeks, or who plan to participate in another human study during the period of participation in this study. 6)Any other individuals deemed unsuitable for participation in the study by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Evaluation of skin conditions 1) VISIA facial imaging Analysis 2) Trans-epidermal water loss 3) Stratum corneum moisture content 4) Mexameter score

Secondary

MeasureTime frame
Subject self-assessment

Countries

Japan

Contacts

Public ContactSindhu Thangavel

ROHTO Pharmaceutical Co., Ltd. New Business Development Division/ Rohto Science Hub Tokyo, Tokyo Skin Lab

hsrpd@rohto.co.jp03-6832-6013

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026