Study of the effects of lactic acid bacteria intake on skin condition and inflammation-related markers in adult men and women with atopic predispositio
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000046242
- Lead Sponsor
- EP Mediate Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 44
Not provided
(1) Subjects who regularly use foods rich in lactic acid bacteria, health foods, and medicines at least three times a week. (2) Subjects who routinely take health foods that may affect the test results. (3) Subjects with experience in aesthetic medicine that affect the measurement site. (4) Subjects who received aesthetic medicine or hormone replacement therapy other than the measurement site from one year ago. (5) Subjects who have undergone esthetic treatment, scrubbing, or hair loss on the skin at the measurement site from one month ago to the end of the study. (6) Subjects who plan to get a sunburn due to long hours of outdoor work, etc. from one month ago to the end of the study. (7) Subjects who have a habit of washing their bodies by giving a strong stimulus to the measurement site. (8) Subjects who regularly use bath salts or subjects who have a habit of taking a hot spring at a frequency of 1 day or more a month. (9) Subjects with skin disorders at the measurement site. (10) Subjects who feel that rough skin occurs at the measurement site before and after menstruation. (11) Night and day shift worker. (12) Subjects who plan to travel abroad during the research period. (13) Subjects who have serious diseases, or diseases that affect the secretion of sex hormones, or have a history thereof. (14) Subjects who may develop allergic-like symptoms with research foods. (15) Subjects with a disease under treatment that affects the evaluation of this study, or with a history of serious illness. (16) Subjects whose pre-examination test values are significantly out of the reference range. (17) Subjects who have participated in other clinical studies within one month or will participate in. (18) Subjects who are planned to become pregnant or are pregnant or lactating. (19) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. (20) Subjects judged as unsuitable for the study by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method