跳至主要内容
临床试验/JPRN-UMIN000025667
JPRN-UMIN000025667已完成未知

A study on the dermatological efficacy of oral administration of beauty capsule - Evaluation of beauty ingredient for skin

SOUKEN Co., Ltd0 个研究点目标入组 30 人开始时间: 2017年1月18日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
30

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
25years-old 至 49years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • -Subjects who go to hospital regularly or went to hospital within the past 1 month for disease: skin, gastrointestinal system, liver, kidney, heart, blood pressure, and physical deconditioning. (Manual therapeutics, chiropractic and massage are not included.) -Subjects who are routinely taking oral medicine or applying external use medicine (ex. hypnotic, analgesic, anti-histamine, rhinitis drug, hormone preparation, cathartic, intestinal regulator, and others). -Subjects who have received medical cosmetic treatment before. -Subjects who have food or drug allergies. -Subjects who are pregnant, could be pregnant in near future, or are breast feeding. -Subjects who are participating in another clinical study. -Subjects who are deemed inappropriate to participate in this study by the principle investigator.

研究者

相似试验