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Verification of the effect of skin function improvement by intake of lactic acid bacteria.

Verification of the effect of skin function improvement by intake of lactic acid bacteria. - Verification of the effect of skin function improvement.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000035719
Enrollment
80
Registered
2020-01-30
Start date
2019-01-30
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 adults

Interventions

Test food: ingestion of food containing lactic acid bacteria 1 cupsule/day, 8 weeks Pracebo food: ingestion of food not containing lactic acid bacteria 1 cupsule/day, 8 weeks

Sponsors

Shiba Palace Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Japanese men and women aged 35 to 59 years old at the time of acquiring consent 2) Persons who care about dry skin 3) Persons who feel sagging skin 4) Persons who are aware of rough skin 5) Persons who are aware of rough skin due to drying, etc. on either the right cheek, the right neck, the upper back, the right shank, the right foot back, or the left cheek, or who have itching symptoms (it is desirable when there is desquamation), or who have flaky skin after bathing, every year from October to March 6) Persons who can stop drinking alcohols from the day before the observation date until the end of the measurement on the observation day 7) Persons who received a sufficient explanation of the purpose of this exam, have the capacity to consent, volunteer for participation after understanding well, and who agreed in writing to participate in this study 8) Persons with stains on their right cheek

Exclusion criteria

Exclusion criteria: 1) Persons who are judged inappropriate by the examining supervisor or doctor in charge of examination 2) Persons with chronic skin symptoms such as atopic dermatitis 3) Persons who used cosmetics containing hyaluronic acid, collagen, ceramide, vitamins etc. within 1 month before start of use 4) Persons who ingested supplements containing hyaluronic acid, collagen, ceramide, vitamins etc. within 1 month before start of use 5) Persons taking or planning to take medicine with hay fever 6) Persons who currently go to dermatology department 7) Persons participating in a test taking other foods or medicines, or applying cosmetics and medicines etc, or participated in similar exams in less than 3 months 8) Persons participating in other clinical trials 9) During pregnancy or planned, or those who are breastfeeding 10) Persons who may have an allergy such as having a history of hypersensitivity to the test article 11) Persons who are likely to have allergic symptoms depending on the test article components 12) Persons with significant abnormalities in the skin condition of the test site (cheek, upper back, neck, elbow, paw) 13) Persons who have chronic illness and regularly use medication 14) Persons who have athema 15) Persons with soy allergy

Design outcomes

Primary

MeasureTime frame
Changes in skin function before ingestion and after ingestion period

Countries

Japan

Contacts

Public ContactKo MASUDA

SOUKEN Co., Ltd Management Division

k_masuda@mail.souken-r.com03-5408-1555

Outcome results

None listed

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