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临床试验/NCT02550548
NCT02550548已完成1 期

Incretin Action in Physiology and Diabetes

David D'Alessio, M.D.1 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2016年4月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
39
试验地点
1
主要终点
Beta cell sensitivity

研究概览

简要总结

This project is designed to advance understanding of the incretin effect in health and disease. This system of gut-islet linkage is essential for normal glucose tolerance, impaired in T2DM, and amenable to therapeutic intervention. However, there are important gaps in understanding incretin function that limit application of this system; this project will address several of these. A secondary, but critical aspect of this research is focus on inter-individual variation in the physiology of the incretin system. This is a novel direction for research in this field and is critical to advancing the concept of individualized medical care in diabetes by establishing whether there is a physiologic basis for predicting the existence of responders and non-responders to incretin therapies.

Currently, we have described only Aim 1 from this grant in this protocol registration. While Aim 2 and 3 are described in the grant, Aim 1 will be conducted first and the results from this Aim and / or the publication of other results in the field may affect the approach to Aims 2 and 3.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • healthy adult volunteers
  • fasting plasma glucose value ≤ 95 mg/dL, measured at screening visit
  • HbA1c ≤ 5.9%, measured at screening visit

排除标准

  • history of diabetes diagnosis, including gestational diabetes
  • presence of Type II diabetes mellitus among any first degree family members
  • rheumatoid arthritis
  • inflammatory bowel disease
  • unstable angina or uncompensated heart failure
  • pulmonary disorders including COPD and asthma
  • malabsorptive GI disease, such as celiac disease, or gastric bypass
  • significant hepatic disease
  • renal insufficiency (eGFR < 60 mL/kg/min)
  • anemia (hematocrit < 34%) as measured at screening visit
  • pregnancy
  • uncontrolled hypertension
  • consumption of daily medications that alter glucose metabolism or GI function (glucocorticoids, psychotropics, narcotics, metoclopramide)

研究组 & 干预措施

GIP infusion

Experimental

During a 240 minute hyperglycemic clamp, subjects will have (after 90 minutes of the clamp) GIP infused at 4 incremental dosages, (initial dose will be 2.0 ng/kg/min, followed by 4.0, 8.0, and 16.0 ng/kg/min). Each dose will be infused continuously for 30 minutes, followed immediately by the next higher dose. The total time of this procedure is 240 minutes.

干预措施: GIP infusion (Drug)

GLP-1 infusion

Experimental

During a 240 minute hyperglycemic clamp, subjects will have (after 90 minutes of the clamp) GLP-1 infused at 4 incremental dosages, (initial dose will be 1.0 ng/kg/min, followed by 2.0, 3.0, and 4.0 ng/kg/min). Each dose will be infused continuously for 30 minutes, followed immediately by the next higher dose. The total time of this procedure is 240 minutes.

干预措施: GLP-1 infusion (Drug)

GIP + GLP-1 infusion

Experimental

During a 240 minute hyperglycemic clamp, subjects will have (after 90 minutes of the clamp) GIP + GLP-1 infused simultaneously at 4 incremental dosages (doses will be half the amounts described above). These doses will be infused continuously for 30 minutes, followed immediately by the next higher doses. The total time of this procedure is 240 minutes.

干预措施: GIP infusion (Drug)

GIP + GLP-1 infusion

Experimental

During a 240 minute hyperglycemic clamp, subjects will have (after 90 minutes of the clamp) GIP + GLP-1 infused simultaneously at 4 incremental dosages (doses will be half the amounts described above). These doses will be infused continuously for 30 minutes, followed immediately by the next higher doses. The total time of this procedure is 240 minutes.

干预措施: GLP-1 infusion (Drug)

GIP + Ex-9 infusion

Experimental

During a 240 minute hyperglycemic clamp, subjects will have (after 90 minutes of the clamp) GIP infused at 4 incremental dosages (as described above) with Ex-9 infused at a steady dose of 2.5 mcg/kg/min starting 90 minutes before the GIP infusion and maintained throughout the clamp experiment. The total time of this procedure is 240 minutes.

干预措施: GIP infusion (Drug)

GIP + Ex-9 infusion

Experimental

During a 240 minute hyperglycemic clamp, subjects will have (after 90 minutes of the clamp) GIP infused at 4 incremental dosages (as described above) with Ex-9 infused at a steady dose of 2.5 mcg/kg/min starting 90 minutes before the GIP infusion and maintained throughout the clamp experiment. The total time of this procedure is 240 minutes.

干预措施: Ex-9 infusion (Drug)

结局指标

主要结局

Beta cell sensitivity

时间窗: 30 minute infusion periods

Beta-cell sensitivity for each incretin will equal the slope of the insulin secretion rate divided by the specific incretin level (GLP-1 or GIP)

次要结局

未报告次要终点

研究者

发起方
David D'Alessio, M.D.
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

David D'Alessio, M.D.

Professor, Division Chief of Endocrinology

Duke University

研究点 (1)

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