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临床试验/KCT0009186
KCT0009186已完成Unknown

A 24-Week, Randomized, Double-blind, Placebo-controlled Clinical Study to Evaluate the Efficacy and Safety of Proso Millet and Wheat Extract(Keranat™) on Hair Health

ovarex0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
100

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
19(Year) 至 60(Year)(—)
性别
All

入选标准

  • 1) Age 19 and 60
  • 2) Hair gloss score of 3 or less and a hair damage score of less than 18 according to the visual evaluation classification method.
  • 3) Willing to maintain the same hairstyle, hair color, hair length, and hair regimen throughout the study period.
  • 4) Subject must be able to comprehend and voluntarily sign study procedures
  • and consent forms.

排除标准

  • 1) Those diagnosed with and receiving treatment for the alopecia within 3months before screening(androgenetic alopecia, alopecia areata, Telogen effluvium, etc.)
  • 2) Use of that may affect hair or hair loss symptoms treatment medicine, dietary supplements, or treatments containing herbal medicine ingredients within 3 months before screening.
  • 3) Any active scalp or skin disease that may interfere with the study treatment and evaluations.
  • 4) Pregnancy or breastfeeding or planning pregnancy
  • 5) Case of abnormal values at creatinine (excess at the upper limit of the reference range)
  • 6) Case of abnormal values at ALT or AST (2 times excess at the upper limit of the reference range)

研究者

发起方
ovarex

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Evaluate the Efficacy and Safety of Proso Millet and... | 临床试验