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临床试验/TCTR20170608002
TCTR20170608002已完成未知

Open-label clinical trial on the effect of “Nature’s Own” instant brown rice powder supplementation on glycaemic control in patients with type 2 diabetes mellitus not adequately controlled with oral hypoglycaemic agents

ili Husniati Yaacob0 个研究点目标入组 64 人开始时间: 2017年6月8日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
64

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
18 Years 至 70 Years(—)
性别
All

入选标准

  • •Age between 18 and 70 years old
  • •Diagnosed with diabetes of more than 6 months
  • •On at least one oral hypoglycaemic agent(s)
  • •HbA1c 7-9% (within the last 3 months on recruitment)
  • • Agree not to take other beverages, herbal or nutritional supplements for the duration of the study.

排除标准

  • •Severe diabetic complication(s) including end-stage renal disease and proliferative retinopathy.
  • •Pregnancy
  • •On insulin therapy

研究者

发起方
ili Husniati Yaacob

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