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A Study for the Effect of Food Containing Ceramide on Skin Quality

A Study for the Effect of Food Containing Ceramide on Skin Quality - A Study for the Effect of Food Containing Ceramide on Skin Quality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000016504
Enrollment
70
Registered
2015-02-20
Start date
2015-02-21
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

Effect of Food Containing Ceramide on Skin Quality

Interventions

Sponsors

TES Holdings Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: [1]Japanese males and females aged 20-60 years [2]Individuals who are healthy and do not treat any disease [3]Individuals who are aware of skin dullness or dryness [4]Individuals who sign the consent document after explanation of this study

Exclusion criteria

Exclusion criteria: [1]Individuals using medical products [2]Individuals with skin disease, such as atopic dermatitis, or strange skin conditions disease at measurement points [3]Individuals who are sensitive to test products [4]Individuals with probable seasonal allergy, such as pollinosis, during the test period [5]Individuals who used cosmetics corresponding to quasi-drug or having whitning or moisturizing effect in the past 1 month or will ingest those foods during the test period [6]Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplyments claiming whitning effect in the past 1 month or will ingest those foods during the test period [7]Individuals who will get sunburned during the test period [8]Individuals who conducted actions, such as hormone replacement therapy, beauty treatment or cosmetic medicine, or diseasae treatment requiring hospital admission, to affect measurement points in the past 3 months [9]Individuals who are alcohol dependent or have other mental disabilities [10]Individuals with possible changes of life style, such as working a night shift or conducting a long-term travel, during the test period [11]Individuals who participated in other clinical studies in the past three months [12]Individuals who are or are posslibly, or are lactating [13]Individuals judged inappropriate for the study by the principal

Design outcomes

Primary

MeasureTime frame
Color-difference Transepidermal water loss Skin moisture content Skin texture

Countries

Japan

Contacts

Public ContactToshiyasu Tamura

TES Holdings Co., Ltd Department of Clinical Trial

info@tes-h.co.jp03-6801-8480

Outcome results

None listed

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