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临床试验/ISRCTN83602901
ISRCTN83602901已完成不适用

A randomized, double-blind, parallel study to compare the relative absorption of UltraSOL Curcumin and Curcumin reference product

OmniActive Health Technologies Ltd0 个研究点目标入组 15 人开始时间: 2017年3月21日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
15

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

性别
All

入选标准

  • 1. Normal healthy individuals
  • 2. Age 18-55
  • 3. Males and females
  • 4. Must be able to perform required testing
  • 5. Participants agreed to sign an informed consent form

排除标准

  • 1. Pregnancy
  • 2. Use of prescription medications
  • 3. Gastrointestinal conditions
  • 4. Diabetics
  • 5. Alcohol and/or substance abuse history, and/or allergies to turmeric or curcumin
  • 6. Subjects consuming any foods or supplements containing curcumin

研究者

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