JPRN-UMIN000050034
Not yet recruiting
未知
A study to evaluate on improvement of skin conditions by the supplementation with lactic acid bacteria - placebo-controlled, randomized, double blind, parallel-group comparison method - - A placebo-controlled, randomized, double-blind, parallel-group study to evaluate of lactic acid bacteria on the skin functions
ConditionsHealthy subjects
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Healthy subjects
- Sponsor
- Kaneka Corporation
- Enrollment
- 60
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •Subjects who met the following exclusion criteria are excluded from the study: 1\) regularly use of medicines or supplements for the skin, or regularly user of probiotics supplements 2\) have skin disease symptoms such as atopic dermatitis, or scars/ inflammation at the test sites 3\) have severe hay fever / allergic symptoms on face 4\) have food allergies 5\) have disease such as hepatic, renal, gastrointestinal, cardiac, respiratory, endocrine, or metabolic diseases 6\) have a history of cosmetic or medical treatments, hormone replacement therapy within the past 6 months, or intend to undergo such treatments during the study period 7\) cannot refrain from undergoing tanning / visiting strong sunlight area during the study period 8\) cannot refrain from direct sunlight for sports, etc 9\) have digestive diseases / a history of digestive surgery 10\) Pregnant, lactating, or intending to become pregnant 11\) Drinker (20 g/day or more of pure alcohol for 4 or more days per week), or cannot abstain from alcohol for 2 days prior to each examination. 12\) Shift workers, late night workers, or have a plan of travel abroad 13\) cannot avoid changing / addition of skin care products 14\) cannot avoid shaving the skin for 7 days prior to the date of each examination 15\) participated in other studies within 1 month prior to the date of informed consent, or have a plan to participate in other studies during this study. 16\) deemed inappropriate by the corresponding investigator with a medical license
Outcomes
Primary Outcomes
Not specified
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