A Single Blinded and Cross over study to assess the bioavailability of CurQfen in comparison with normal unformulated Curcumin supplementation in healthy volunteers.

Akay Flavours Aromatics PvtLtd0 个研究点目标入组 50 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•1. Healthy volunteers of age 20 to 55 years of either sex who are not involved in any regular medication or supplementation.
•2. Subjects who are willing to give their written informed consent and comply with the protocol requirements.

•1. Patient who took turmeric contained food 2 days prior to screening
•2. Pregnant or lactating women.
•3. Subjects with known hypersensitivity to the investigational products.
•4. Subjects who have participated in any clinical trial in the past 1 month.
•5. Any subjects found to have entered in to the study in violation of this protocol or if the subject is uncooperative during the study.
•6. Any other condition that in the opinion of the investigator that does not justify the subjectâ??s participation in the trial

发起方

Akay Flavours Aromatics PvtLtd