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临床试验/NCT01934816
NCT01934816终止不适用

Effects of KATP Channel Blockers on GLP-1 and Its Analogues' Mediated Microvascular Function

Katarina Kos2 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2013年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
2
试验地点
2
主要终点
Change in skin blood flow to GLP-1 and its analogues

研究概览

简要总结

This study aims to examine the involvement of KATP channels on the microvascular actions of the incretin GLP-1 and its analogues in healthy individuals and to determine whether the acute oral administration of different KATP channel blockers which are oral medications for Type 2 diabetes such as Glibenclamide and Glimepiride differentially modulate the microvascular responses in these individuals.

详细描述

In addition to the glucose lowering effect, incretin based therapies have also an effect on the vascular system. Previous animal work and initial human studies suggest that incretins may be cardioprotective and act as vasodilators through opening of KATP channels.

Initial evidence suggests that beneficial vascular effects of incretin modifying agents may be nullified by the co-current treatment of the sulfonylurea (SU) drug glibenclamide. The investigators hypothesis is that the GLP-1 and SUs may have conflicting effects on the KATP channels and thus vascular function.

Interestingly the vascular actions of GLP-1 were not modified by a different treatment SUs called glimepiride, thereby raising the possibility that SUs differentially modulating the vascular actions of GLP-1 though this remains controversial.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • BMI ≤ 25 kg/m2

排除标准

  • current or past history of diabetes (HbA1C more or equal 45mmol/mol)
  • history of postprandial hypoglycaemia and dumping syndrome
  • established cardiovascular disease
  • established cerebrovascular disease
  • blood pressure ≥ 140/85 mmHg
  • Raynaud's disease
  • severe impairment of renalhepatic, thyroid or adrenocortical function
  • current treatment with any anti-hypertensive treatment
  • lipid lowering therapy or systemic steroids
  • lactation, pregnancy
  • established vascular disease
  • bariatric surgery
  • significant weight change within the last 3 months

结局指标

主要结局

Change in skin blood flow to GLP-1 and its analogues

时间窗: 6 weeks

Skin blood flow will be assessed before and after microinjection of GLP-1 or its analogues and the injection site monitored and compared to sites injected with placebo

次要结局

未报告次要终点

研究者

发起方
Katarina Kos
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Katarina Kos

Senior Lecturer

Royal Devon and Exeter NHS Foundation Trust

研究点 (2)

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