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临床试验/KCT0004592
KCT0004592招募中未知

A 12week, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the evaluation of the efficacy and safety of 7-MEGATM500 on the Skin wrinkle improvement

Vitech0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
30(Year) 至 60(Year)(—)
性别
All

入选标准

  • 1) Adult men and women subjects aged 30 older or under 60
  • 2) The subjects with eye crease grade 3 or higher in visual evaluation
  • 3) The subjects who have agreed to participate in this test prior to the start of the test and have signed a written consent form

排除标准

  • 1) The subjects who have or are currently undergoing treatment for skin diseases such as atopic dermatitis and psoriasis
  • 2) The subjects who are sensitive or allergic to food for testing
  • 3) The subjects with abnormal skin conditions such as spots, acne, erythema, and capillary dilation in the test area
  • 4) Based on Visit 1, a person who received treatment on the facial (skin stripping, other skin care, etc.) or received treatment on the facial area within 6 months
  • 5) Based on Visit 1, a person who used a skin external substance containing steroids on the facial part or take an oral retinoid/steroid agent within 3 months of the standard visit
  • 6) Based on Visit 1, a person who used functional cosmetic (retinoid agent, retinol, AHA) or moisturizing cosmetic or skin care (LED mask, ion booster, etc.) to improve wrinkles within 2 weeks of visit
  • 7) Based on Visit 1, a person who has taken diet pills (absorbent and antidepressants, appetite suppressants, etc.) and contraceptives or hormones or diuretics within one month
  • 8) Based on Visit 1, a person who has taken health function foods containing antioxidants, hyaluronic acids, collagen, freedom of the moon flower, Omega 3, 6 fatty acids such as violet oil, krill oil, persimmon-nolene acid, affluence of manic tree oil (Omega-7), vitamin A, vitamin C, vitamin E, DHA/EPA, and other medicinal products consumed within two weeks
  • 9) Based on Visit 1, a person who has participated in other interventional clinical tests (including human application tests) within one month of the standard or plans to participate in other interventional clinical tests (including human application tests) after the start of this human application test.
  • 10) AST (GOT) or ALT (GPT) or ?-GTP is three times the normal scope of the testing agency
  • 11) Creatine level is more than twice the test institution's
  • 12) TSH 0.1 µIU/ml or 10 µIU/ml or higher
  • 13) Unregulated hypertension patients (based on measurement after 10 minutes of stabilization, at least 160mmHg of the hydraulic pressure or more than 100mmHg of the relaxant blood pressure)
  • 14) Diabetes patients whose blood sugar is unregulated (over 180 mg/dl in public blood)
  • 15) The subjects with schizophrenia, depression, drug addiction, etc.
  • 16)The subjects who are pregnant, nursing, or planning to conceive within three months;
  • 17) Those who are hospitalized, drug treatment, and rehabilitation treatment for alcohol use ·causing disorder, heart disease, and central nervous disorder through a history investigation
  • 18) Smokers or those who smoke less than a year after quitting smoking
  • 19) A person who is deemed inappropriate for this test by the researcher

研究者

发起方
Vitech

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