A human study to evaluate the skin health improvement effect and safety of ME-100

Kyung Hee University0 个研究点目标入组 110 人开始时间: 待定最近更新: 2020年3月23日

适应症

试验速览

暂无简介。

•1)Subject who voluntarily agree to participate and signs informed consent form
•2)Men and women aged 30 to under 60
•3)Subject who has a dry skin (skin moisture content index below 49AU measured using Corneometer®), eye wrinkles begin to form or have already formed (visual evaluation grade 3 or higher).

•1)Subjects with abnormal skin conditions such as spots, acne, erythema, and capillary dilation in the test area
•2)Subjects who have or are currently undergoing treatment for skin diseases such as atopic dermatitis and psoriasis
•3)Subjects who take contraceptives or hormones or diuretics
•4)Subjects who take a oral retinoid/steroid agent or use a skin external substance containing steroids or retinoids within 3 months before the first visit
•5)Subjects who use a functional cosmetic (retinoid agent, retinol, AHA) to improve wrinkles or moisturizing cosmetic within 2 weeks before the first visit
•6)Subjects who received treatment(skin stripping, lazer, chemical peeling, other skin care, etc.) on the facial area within 1 month or received treatment(botox, filler) on the facial area within 6 months before the first visit
•7)Subjects with diseases such as uncontrolled hypertension, uncontrolled diabetes, renal dysfunction, liver dysfunction, etc.
•8)Subjects who have been continuously consumed any healthy functional food within 1 month before the first visit
•9)Smokers or Subjects who smoke less than a year after quitting smoking
•10)Participation in other human study within 1 month before the first visit
•11)Subjects who are pregnant, nursing, or planning to conceive
•12)Subjects with hypersensitivity to test materials
•13)Any condition that the principal investigator believes may put the subjects at undue risk

发起方