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Epidemiological Study Using Test Products

Epidemiological Study Using Test Products - Epidemiological Study Using Test Products

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060461
Enrollment
9
Registered
2026-01-26
Start date
2026-01-26
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

Healthy people

Interventions

Use once a day or more for one month.

Sponsors

DHC Corporation
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Individuals who participated in the pre-trial and were in their 20s, 40s, or 60s at the time of obtaining consent for the pre-trial (2) Females (3) Individuals who have received sufficient explanation regarding the purpose and content of the main trial, possess the capacity to consent, have fully understood the information, voluntarily applied to participate, and are able to provide written consent to participate in the main trial

Exclusion criteria

Exclusion criteria: (1)deemed ineligible for internal structure examinations by medical institutions. (2)factors on the evaluation site skin that may affect test results. (3)history or current condition of atopic dermatitis, or those with an atopic predisposition. (4)undergone cosmetic medical procedures on the evaluation site, or who plan to undergo such procedures during the test period (5)received special skincare treatments on the evaluation site within the past 4 weeks, or who plan to receive such treatments during the test period (6)routinely apply pharmaceuticals or topical medications to the evaluation site (7)changed or newly started using health supplements, basic cosmetics applied to the evaluation site, or sunscreen within the past 4 weeks (8)exposed to ultraviolet rays beyond their normal daily activities within the past 4 weeks, or who plan to do so during the trial period (9)working night shifts or rotating day-night shifts (10)receiving treatment at medical institutions for disease treatment or prevention at the time of consent acquisition, or individuals judged to be in a condition requiring treatment (11)history of serious diseases affecting glucose metabolism, lipid metabolism, liver function, kidney function, the circulatory system, respiratory system, endocrine system, immune system, or nervous system (12)history of alcohol or drug dependence (13)risk of developing allergies to cosmetics or food (including those who experienced skin abnormalities such as rashes from cosmetics within the past year) (14)pregnant or breastfeeding at the time of consent acquisition,wish to become pregnant during the trial period (15)participated in another human trial within the past 4 weeks, or who plan to participate in another human trial during the scheduled period of this trial (16)silver fillings or dental implants (17)deemed unsuitable for trial participation by the Principal Investigator (or Investigator)

Design outcomes

Primary

MeasureTime frame
[Lip]stratum corneum moisture content, transepidermal water loss, skin viscoelasticity, dermal thickness, skin pH, stratum corneum condition, morphological evaluation via image analysis, internal structural changes via image analysis [Face]changes in skin condition indicators such as pigmentation, wrinkles, and pores

Countries

Japan

Contacts

Public ContactJunichiro Nagumo

DHC Corporation Fragrance and Cosmetics Unit

jnagumo@dhc.co.jp03-5765-9518

Outcome results

None listed

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