JPRN-UMIN000034061
Completed
未知
A study for the effect of microorganism containing foods on skin condition. A randomized, double-blind, placebo-controlled, Parallel-group comparison trial. - A study for the effect of microorganism containing foods on skin condition
Conditionsone (Healthy adults)
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- one (Healthy adults)
- Sponsor
- TES holdings Co., Ltd.
- Enrollment
- 70
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\)Individuals who have diseases with medications. 2\)Individuals who receive medications within 1 month before examination. 3\)Individuals who have a medical history of serious disease of liver, kidney, heart, lung, blood and digestive tract. 4\)Individuals who have severe skin disorder, such as skin burn. 5\)Individuals who are difficult to take samples for gene expression analysis. 6\)Individuals who refuse to disclose their biological sexes. 7\)Individuals who may have an allergic symptom to test foods, or individuals who may have a serious allergic symptom to other foods, or medicaments. 8\)Individuals who are alcoholic or have mental disorders. 9\)Individuals who have a smoking habitat. 10\)Individuals who will change their life style during test period, such as traveling for a long period. 11\)Individuals who cannot keep from direct sunlight exposure, such as tanning activities, during test period. 12\)Individuals who may occur seasonal allergic symptoms, such as hay fever, and receive medications during test period. 13\)Individuals who have severe menopausal symptoms. 14\)Individuals who are taking or took foods or medications, specified for skin conditions or are planning to take these foods during test period. 15\)Individuals who cannot stop eating foods related with this test foods during test period. 16\)Individuals who have severe anemia. 17\)Individuals who donate more than 200 ml of blood within 1 month or more than 400 ml of blood within 3 months. 18\)Individuals who have a surgical or treatment history on the regions of measurement within 6 months. 19\)Individuals who are pregnant, breastfeeding, or planning to be pregnant in the near future. 20\)Individuals who are participating or participated in another clinical trial within the last 3 months. 21\)Individuals who and whose family living with them work for a company manufacturing or selling healthy foods or cosmetics. 22\)Individuals who are judged as unsuitable for participating this study by the investigator.
Outcomes
Primary Outcomes
Not specified
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