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临床试验/NCT02007577
NCT02007577已完成不适用

Beneficial Effect of Salicylates: Insulin Action, Secretion or Clearance?

Stanford University1 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2010年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
41
试验地点
1
主要终点
Quantification of Insulin Action With the Insulin Suppression Test (IST)

研究概览

简要总结

The possibility that obesity-associated inflammatory changes may play a role in the pathogenesis of type 2 diabetes (2DM) has led to increased interest in the possibility that salicylates might represent a useful treatment to improve glucose tolerance. Several studies, performed in patients with 2DM, as well as in nondiabetic, obese individuals, have demonstrated that salicylates have beneficial effects on glucose and insulin metabolism, but have not led to a coherent view as to the mechanism(s) involved.

In this research proposal we will use specific methods to quantify insulin mediated glucose uptake (IMGU), glucose-stimulated insulin secretion rate (GS-ISR), and insulin clearance (I-Cl) in overweight/obese, nondiabetic, insulin resistant individuals. We will use the insulin suppression test (IST) to quantify IMGU in nondiabetic, overweight/obese volunteers to identify those individuals who are sufficiently insulin resistant to be enrolled in this study. We will then use the graded glucose infusion technique in these insulin resistant subjects to generate specific measures of both GS-IS and I-Cl. Following these baseline measurements, salsalate or placebo will be administered for one month to the participants, after which time the IST and the graded glucose infusion will be repeated to quantify and compare the changes in IMGU, GS-ISR, and I-Cl that have resulted from salsalate versus placebo. These results will provide for the first time quantitative data of the effect of salicylates on IMGU, GS-ISR, and I-Cl in overweight/obese, insulin resistant, nondiabetic individuals.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single (Participant)

入排标准

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

入选标准

  • Healthy volunteers,
  • BMI 25-35kg/m2,
  • Without severe anemia, kidney, liver disease or any current GI ulcers or bleeding
  • Or on any medication contraindicated with salsalate

排除标准

  • Recent history of GI bleed or ulcers,
  • CVD or on anticoagulants
  • Severe kidney or liver disease
  • Allergies to aspirin
  • Taking aspirin or anti inflammatory medication on a regular basis and cannot be taken off for the duration of the study

研究组 & 干预措施

salsalate 3500mg in 2 divided doses a day

Active Comparator

Participants will take 3, 500 mg tablets with breakfast and 4, 500 mg tablets with dinner

干预措施: salsalate (Drug)

placebo

Placebo Comparator

Participants will take 3 placebo tablets with breakfast and 4 placebo tablets with dinner

干预措施: Placebo (Drug)

结局指标

主要结局

Quantification of Insulin Action With the Insulin Suppression Test (IST)

时间窗: after treatment for one month

Compare changes in insulin sensitivity as assesses by the IST before and after treatment between salsalate and placebo group

次要结局

  • Quantification of Insulin Clearance With the Graded Glucose Infusion Test (GGIT)(one month on treatment)

研究者

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

Gerald M Reaven

Professor Emeritus

Stanford University

研究点 (1)

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