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临床试验/KCT0008816
KCT0008816已完成Unknown

Pilot Study to prove the reproducibility of the intestinal environment of PMAS(Pharmaceutical Meta-Analytical Screening) System through the production of Equol after intake of Soy Isoflavone

HEM Pharma0 个研究点目标入组 36 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
36

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 o Limit(—)
性别
All

入选标准

  • 1. Healthy adults who are 19 years of age or older.
  • 2. Individuals who have willingly and voluntarily agreed to participate in this study.

排除标准

  • 1. Individuals who have a hypersensitivity or allergy to soy materials, such as soy isoflavones.
  • 2. Individuals who have been determined by the tester to be unsuitable for participation in the human application test.
  • 3. Individuals who have used systemic antibiotics within one week prior to Visit 1.
  • 4. Pregnant and lactating women.

研究者

发起方
HEM Pharma

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