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临床试验/NCT04877366
NCT04877366已完成不适用

A Randomized, Double-blind, Placebo- and Active-Controlled, Single-Center, Three-time-period, Crossover Study to Evaluate the Effects of Sprinkled Format REDUCOSE on Post-Prandial Glycemic Response in Asian Patients with Type 2 Diabetes

Société des Produits Nestlé (SPN)4 个研究点 分布在 2 个国家目标入组 30 人开始时间: 2021年7月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
4
主要终点
Post-prandial glycemic excursion (ARMs A and B)

研究概览

简要总结

This is a mechanistic, single-center, double-blind, placebo- and active-controlled, three-time-period, crossover study to evaluate the effect of sprinkled format REDUCOSE compared to placebo (double-blind; confirmative) and active control (open-label; acarbose - explorative) on post prandial glycemia in Asian patients with type 2 diabetes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Double (Participant, Investigator)

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Willing and able to sign written informed consent prior to study entry.
  • Participants who self-identify as Asian; male or female, >18 years of age.
  • Established diagnosis of type 2 diabetes (documented by either HbA1c 6.5 - 10.0% or a documented diagnosis of type 2 diabetes).
  • Treatment naïve or on active therapy with metformin at a daily dose of 500-3000 mg at screening. Dose of metformin must have been stable for at least 3 months prior to screening.
  • Participants must have a hematocrit value greater than or equal to 34.0% for females and 40% for males.
  • Participants must have a hemoglobin value greater than or equal to 11.0 g/dL for females and 13.5 g/dL for males.

排除标准

  • Fasting plasma glucose >220 mg/dl at screening.
  • Impaired kidney function, eGFR of <60 mL/min/1.73 m2 at screening.
  • BMI >35 kg/m
  • Weight ≤ 50 kg.
  • Elevated liver transaminase > 3 ULN at screening.
  • Ongoing or recent (i.e. < 3 month) treatment with any oral or injectable glucose-lowering drug other than metformin.
  • Ongoing or recent (i.e. < 3 month) injectable insulin therapy.
  • Ongoing or recent (i.e. < 3 month) weight loss interventions (e.g. dietary weight loss programs) or any history of bariatric surgery or any documented weight loss >5% within previous 6 months.
  • Ongoing or recent (i.e. < 3 month) treatment with anorectic drugs, systemic steroids, medications known to affect gastric motility, or any condition known to affect gastro-intestinal integrity and food absorption.
  • Major medical/surgical event requiring hospitalization in the last 3 months.
  • Known allergy and intolerance to product components or paracetamol.
  • Alcohol intake higher than 2 servings per day. A serving is 0.4 dl of strong alcohols, 1 dl of red or white wine, or 3 dl of beer.
  • Are unable to comply with protocol procedures in the opinion of the investigator.
  • Have a hierarchical link with the research team members.
  • Positive pregnancy test or breast-feeding at screening.
  • Participants who have been dosed in another clinical study with any investigational drug/new chemical entity within 30 days or 5 half-lives (whichever is longer) prior to screening.
  • Donation of blood or significant amount of blood loss within 8 weeks prior to screening. Participants must also agree to not donate blood within 8 weeks after their last visit.

结局指标

主要结局

Post-prandial glycemic excursion (ARMs A and B)

时间窗: 0 ,15, 30, 60, 120, and 180 minutes.

Incremental area under the curve post-prandial glycemic excursion (iAUC 0-1h, iAUC 0-2h, iAUC 0-3h).

次要结局

  • Plasma glucose Tmax (ARMs A and B)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Plasma interleukin-6 (ARMs A and B)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Total glucose (All ARMS)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Plasma GLP-1 (ARMs A and B)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Serum insulin (All ARMs)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Plasma GIP (ARMs A and B)(0 ,15, 30, 60, 120, and 180 minutes.)
  • 2h post-prandial glucose levels (ARMs A and B)(0 ,15, 30, 60, and 120 minutes.)
  • Plasma glucose iCmax (ARMs A and B)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Plasma glucose AUC (ARMs A and B)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Gastric emptying (ARMs A and B)(0 ,15, 30, 60, 120, and 180 minutes.)
  • Matsuda Index (ARMs A and B)(0, 30, 60, and 120 minutes.)

研究者

发起方
Société des Produits Nestlé (SPN)
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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