Study to confirm the effect of continuous ingestion of food containing Lactobacillus brevis subsp. coagulans (Labre) on skin moisture.
- Conditions
- Healthy adult women
- Registration Number
- JPRN-UMIN000051886
- Lead Sponsor
- Medical Corporation Hokubukai Utsukushigaoka Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- Female
- Target Recruitment
- 100
Not provided
(1) Subjects who have a history of heart, liver, kidney disease, organ damage, diabetes, or other serious diseases (2) Subjects who have a history of gastrointestinal surgery (excluding appendectomy) (3) Subjects who are currently receiving medical drug treatment (4) Subjects who are pregnant, wish to become pregnant during the study, or are breastfeeding (5) Subjects who regularly take health functional foods, health foods, supplements, etc. that claim to enhance skin moisture and skin elasticity (6) Subjects who have factors that may affect the evaluation of this research at the measurement site (skin diseases such as atopic dermatitis, trauma, burn,inflammation, acne, wart, Japanese tattoos,modern tattoos, etc.) (7) Subjects who have undergone hyaluronic acid injection or Botox injection at the measurement site (8) Subjects who take foods or supplements containing lactobacilli or bifidobacteria 3 times or more a week (Suguki pickle, bran pickle, kimchi, "Labre capsules", etc.) (9) Shift workers, including late-night shifts (10) Subjects who drink more than 60 g pure alcohol equivalent/day on average (11) Subjects who smoke an average of 21 cigarettes or more per day (12) Subjects who donated blood within 3 months at screening (13) Subjects who are participating in clinical research or monitoring (food, pharmaceuticals, cosmetics) other than this research, or plan to participate during this research period (14) Subjects who are judged to be inappropriate for this study with other reasons by the principal investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method