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临床试验/NCT02999321
NCT02999321已完成不适用

The Effects of Aspartame on Appetite, Body Composition and Oral Glucose Tolerance

Purdue University2 个研究点 分布在 1 个国家目标入组 93 人开始时间: 2016年8月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
93
试验地点
2
主要终点
change oral glucose tolerance

研究概览

简要总结

Assess the impact of chronic use of aspartame on glycemia, appetite and body composition.

详细描述

Participants will be randomly assigned to one of three parallel arms: 0% (water), 5 mg, 15mg aspartame. Participants will have an oral glucose tolerance test at the beginning and end of a 12 week intervention. . Participants will report to the lab weekly for 12 weeks to pick up their next week's intervention products and measurements for body weight, waist circumference, blood pressure and heart rate. They will consume their intervention products daily for 12 weeks. They will record appetite sensations and collect a 24 hour urine sample at weeks 0, 4, 8, and 12.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
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

  • BMI 18-25
  • Fasting blood sugar between 72 and 108 mg/dl via capillary finger-stick.

排除标准

  • 未提供

研究组 & 干预措施

0% aspartame (water)

Experimental

participants will not have any aspartame, this is a control.

干预措施: water (Other)

15mg aspartame

Experimental

participants will receive 5 mg aspartame in a beverage, and 10mg in capsules.

干预措施: aspartame (Other)

5 mg aspartame

Experimental

participants will receive 5 mg aspartame in a beverage.

干预措施: aspartame (Other)

结局指标

主要结局

change oral glucose tolerance

时间窗: week 12 4 hours

sample taken at time point 0

次要结局

  • Appetite(every hour for 1 day at week 12)
  • Body composition(week 12)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard Mattes

Professor of Nutrition Sciences

Purdue University

研究点 (2)

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