JPRN-UMIN000041618已完成未知
Inhibitory effect of the test food on ultraviolet-induced skin damage. - Inhibitory effect of the test food on ultraviolet-induced skin damage.
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 24
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 30years-old 至 60years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Subjects with photosensitivity disorder. 2)Subjects who take medicine that affect light sensitivity of skin. 3)Subjects who regularly go to a dermatology office. 4)Subjects who continuously take medicine, quasi-medicine, functional food or supplement which advocate or emphasize efficacy for which is evaluated in the trial. 5)Subjects who have skin disease or abnormality such as atopic dermatitis. 6)Subjects who may perform physical activity in the sunlight for a long time during test period. 7)Subjects who take anti-inflammatory medicine at least once a month. 8)Shift worker. 9)Subjects who receive or require medical or prophylactic treatment. 10)Subjects who have a medical history for severe disease or abnormality in glucose or lipid metabolism, endocrine or nerve system, or for psychiatric disorder. 11)Subjects who have a medical history or present illness of serious hepatopathy, kidney damage, heart disease, hematological and blood disease. 12)Subjects who have a medical history of serious gastrointestinal disease. 13)Subjects who have a medical history of alcoholism or drug addiction. 14)Subjects who have risk for allergy related to test foods. 15)Subjects who have s damage or inflammation on the measurement sites. 16)Subjects who have Severe anemia. 17)Subjects whose BMI is over 30.0 kg/m2 18)Subjects who smoke. 19)Subjects who will develop seasonal allergy symptoms like hay fever and take medicine. 20)Subjects who had been conducted an operation or beauty treatment on the measurement sites within the past 6 months. 21)Subjects who frequently intake food which might affect skin color. 22)Subjects who show abnormality in blood test during screening and test period. 23)Possible pregnancy, pregnancy and lactation 24)Subjects who were involved in another clinical studies within 4 weeks prior to the trial, or who will participate in another clinical studies. 25)Subjects who are judged to be inappropriate for the study by the principal investigator.
研究者
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