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Verification test of the effect of continuous use of the test product on skin condition

Verification test of the effect of continuous use of the test product on skin condition - Verification test of the effect of continuous use of the test product on skin condition

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055729
Enrollment
10
Registered
2024-10-08
Start date
2024-10-09
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 subject

Interventions

Test product 1 applies to the designated area for 6 weeks Test product 2 applies to the designated area for 6 weeks Test product 3 applies to the designated area for 6 weeks Control product applies

Sponsors

M&I Science CORP.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Japanese women between the ages of 20 and 65 at the time of obtaining written consent. 2.Subject who is aware of their skin dryness. 3.Subject who is able to strictly follow the instructions for use of the study products during the study period. 4.Subject who has been fully informed of the purpose and content of the study, is capable of consenting, understands the study well, voluntarily volunteers to participate in the study, and agrees to participate in the study in writing.

Exclusion criteria

Exclusion criteria: 1.Subject who has skin diseases (atopic dermatitis, contact dermatitis, etc.), traumatic injuries, or subjective symptoms such as pain that may affect the examination. 2.Subject who is attending a dermatological clinic at the time of consent. 3.Subject who has a serious disease or disorder that would make participation in the study a risk to the subject. 4.Subject with a history of hypersensitivity to cosmetics. 5.Subject is using or will use during the study period any drugs, health foods or supplements that are known to affect the study. 6.Subject is receiving hormone replacement therapy. 7.Subject who has a history of cosmetic therapy that may affect the study site. 8.Subject who has used cosmetic devices or cosmetic appliances within 1 month of obtaining consent. 9.Subject who has participated in another clinical trial (research) within 1 month of obtaining consent or who plans to participate in another clinical trial (research) during the study period. 10.Subject who is currently pregnant or lactating, or who may become pregnant or lactating during the study period. 11.Subject who is considered as an inappropriate candidate by the doctor in charge.

Design outcomes

Primary

MeasureTime frame
Stratum corneum water content

Secondary

MeasureTime frame
Transepidermal water loss, Texture, Skin viscoelasticity

Countries

Japan

Contacts

Public ContactMasao Matsuoka

M&I Science CORP. Clinical Development Department

m.matsuoka@mis21.co.jp06-7878-6780

Outcome results

None listed

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