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临床试验/CTRI/2023/08/056330
CTRI/2023/08/056330已完成3 期

A Prospective, Randomised, Placebo Controlled Study to Evaluate the Impact ofGLUBLOC™ on postprandial blood glucose and insulin levels in healthy individuals post highcarbohydrate meal intake. - NI

My Pura Vida Wellness Pvt Ltd0 个研究点目标入组 35 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
35

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

  • Aged between 18–60 years,
  • BMI between 20 and 29.9 kg/m2
  • Fasting blood glucose = 5.7 mmol/l (or) = 99 mg/dl

排除标准

  • History of hypersensitivity to any of the investigational product, excipients, or Any known food allergies.
  • Pre-existing medical condition or taking medication known to affect glucose regulation and/or influence digestion and absorption of nutrients
  • History of diabetes mellitus (type I/II) or they used antihyperglycemic drugs or insulin to treat diabetes or related conditions
  • Use steroids, protease inhibitors or antipsychotic medicines as these drugs are known to impact glucose metabolism and body fat distribution.
  • Subjects with the history of uncontrolled hypertension and/or hyperthyroidism.
  • History of alcoholism
  • Subjects with psychiatric or neurological disability or mental health disorder
  • Subjects with serious health conditions such as cardiac disease, renal dysfunction, and cancers.
  • Female subjects who are pregnant or had planned for pregnancy in the following months or were breast-feeding.
  • Subjects who refuse to sign informed consent.
  • According to the investigator’s opinion, participants who are deemed unable to comply with the test requirements or otherwise deemed unsuitable.

研究者

发起方
My Pura Vida Wellness Pvt Ltd

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