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Exploratory Study of Skin Condition Following Use of Test Cosmetics

Exploratory Study of Skin Condition Following Use of Test Cosmetics - Exploratory Study of Skin Condition Following Use of Test Cosmetics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061128
Enrollment
20
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

Apply the three test products (lotion, serum, and cream) twice daily after washing in the morning and evening. Continue this for up to 12 weeks.

Sponsors

ROHTO Pharmaceutical Co., Ltd.
Lead Sponsor
Shin-Kawasaki Eve Clinic for Dermatology and Aesthetic Medicine
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Individuals aged 18 or older at the time of consent acquisition 2) Individuals who have received sufficient explanation regarding the purpose and content of this trial, possess the capacity to consent, voluntarily volunteer to participate after fully understanding, and can provide written consent to participate in this study.

Exclusion criteria

Exclusion criteria: Individuals 1) who used the products containing stem cell culture supernatant within 4 weeks. 2) at risk of developing allergies related to ingredients in this trial cosmetic or to cosmetics. 3) who are pregnant, breastfeeding, may be pregnant, or plan to become pregnant during the study. 4) in other clinical trial within 4 weeks. 5) considered unsuitable for the study by the principle investigator.

Design outcomes

Primary

MeasureTime frame
Skin conditions 1)VISIA's indicators 2)Trans epidermal water loss 3)Stratum corneum moisture content 4)Mexameter's score

Secondary

MeasureTime frame
Subject self-assessment

Countries

Japan

Contacts

Public ContactMiwako Shidomi

ROHTO Pharmaceutical Co., Ltd. Health Science & Data Planning Division

hsrpd@rohto.co.jp03-6832-6013

Outcome results

None listed

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