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临床试验/NCT07762768
NCT07762768尚未招募不适用

Effect of CSIR-Developed High-Protein, Low-Glycaemic Index Rice on Glycaemic Response in Individuals With Prediabetes: An Acute and Subacute Crossover Study

Diabetes Foundation, India1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
36
试验地点
1
主要终点
Study Phase 1: Meal Tolerance Test

研究概览

简要总结

This is a randomized, controlled, two-phase crossover study will be conducted in adults aged 18-60 years with prediabetes to compare the effects of a CSIR-developed high-protein, low-glycaemic index rice with conventional rice. Phase I will evaluate acute postprandial glucose, insulin, C-peptide, GLP-1, and hunger/satiety responses, while Phase II will assess 72-hour continuous glucose monitoring (CGM) outcomes, including mean glucose and glycaemic variability. Eligible participants will be randomly assigned to receive both rice types in a crossover manner, with each participant serving as their own control. Individuals with diabetes, major systemic illnesses, abnormal liver or renal function, pregnancy, or glucose-lowering medication use will be excluded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-60 years
  • Individuals with prediabetes, defined by oral glucose tolerance test (OGTT) as:
  • Fasting plasma glucose ≥100 mg/dL and <126 mg/dL, and/or
  • 2-hour plasma glucose ≥140 mg/dL and <200 mg/dL following ingestion of 75 g anhydrous glucose
  • Willingness to participate and comply with study procedures

排除标准

  • Diagnosed diabetes mellitus
  • Acute infections or any debilitating illness
  • History of hepatic, pancreatic, renal, or cardiovascular disease
  • Abnormal liver or renal function tests
  • Recent (<3 months) weight change ≥5% or use of weight-altering medications
  • Use of glucose-lowering medications
  • Pregnancy or lactation
  • Known allergy or intolerance to study foods
  • Any condition that, in the investigator's opinion, may interfere with study participation

研究组 & 干预措施

Intervention Group

Active Comparator

CSIR-Developed High-Protein, Low-Glycaemic Index Rice

干预措施: Intervention Group (Dietary Supplement)

Control Group

Active Comparator

Conventional Rice

干预措施: Intervention Group (Dietary Supplement)

结局指标

主要结局

Study Phase 1: Meal Tolerance Test

时间窗: 1 day

incremental area under the curve(mg/dL)

次要结局

  • meal tolerance study(1 day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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