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临床试验/CTRI/2020/03/023947
CTRI/2020/03/023947尚未招募未知

A randomized, double-blind, placebo-controlled, clinical study to evaluate the effect CUQ1720 on the postprandial response in healthy subjects and as an adjuvant to metformin in diabetic subjects.

Akay Flavours and Aromatics Private Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

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

入选标准

  • 1. BMI of 18-30 kg/m2

排除标准

  • For Healthy Subjects
  • 1. Fasting Blood Sugar < 110 mg/dl
  • 2. Hb1Ac less than 5.7 %
  • For diabetic Subjects
  • 1.Fasting Blood Sugar >= 120 to <= 150 mg/dl
  • 2.Hb1Ac: Greater than 6.5 %
  • 3.Subjects on metformin 500 mg, twice a day, since past 3 months
  • 4.Females of child bearing age, agree to use approved birth control methods during the study, and have negative urine pregnancy test at screening
  • 5.Subject willing to adhere with their routine diet, physical activity, and general lifestyle throughout the study
  • 6.Must be willing and able to give informed consent and comply with the study procedures.

研究者

发起方
Akay Flavours and Aromatics Private Limited

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