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临床试验/NCT03329651
NCT03329651
已完成
不适用

The Interaction Between Metformin and Acute Exercise

Kristian Karstoft1 个研究点 分布在 1 个国家目标入组 34 人2017年11月10日

概览

阶段
不适用
干预措施
Metformin treatment
疾病 / 适应症
Impaired Glucose Tolerance
发起方
Kristian Karstoft
入组人数
34
试验地点
1
主要终点
Difference in postprandial glycemic control as assessed by mean blood glucose concentration during a 4 hour mixed-meal tolerance test
状态
已完成
最后更新
7年前

概览

简要总结

Physical activity is a first line treatment for patients with type 2 diabetes (T2D), however, the vast majority of patients with T2D do not achieve satisfying glycemic control with physical activity alone, which is why pharmacological treatment with metformin is most often initiated.

It is known that metformin and exercise both activates 5' adenosine monophosphate-activated protein kinase (AMPK) in skeletal muscle and liver, and the activation of AMPK results in many different metabolic effects, including improvements in glycemic control. Because of this similarity in mechanism of action, an interaction between metformin and exercise is plausible, but knowledge in the area is sparse. Thus, the aim of this study is to assess the effects of acute physical activity with and without concomitant metformin treatment, in order to investigate whether an interaction between the two occur.

Subjects with impaired glucose tolerance will be randomized (1:1) to metformin/placebo treatment in a double-blinded way. Following a treatment run-in period of 17 days, two experimental days (one with acute exercise and one without acute exercise), separated by one week, will be performed in each subject.

This registration concerns a sub-study of another study which has previously been registrered at ClinicalTrials.gov (Unique Protocol ID: H-17012307). The specific outcomes in this registration have not previously been registered.

注册库
clinicaltrials.gov
开始日期
2017年11月10日
结束日期
2018年10月1日
最后更新
7年前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
Kristian Karstoft
责任方
Sponsor Investigator
主要研究者

Kristian Karstoft

Principal Investigator

Rigshospitalet, Denmark

入排标准

入选标准

  • Glucose-lowering-medication naïve T2D and/or subjects with impaired glucose tolerance defined as: 2-h plasma glucose (PG) in the 75-g OGTT (7.8-11.0 mmol/L) and/or HbA1c (39-47 mmol/mol)
  • Caucasian
  • BMI \> 25 but \< 40 kg/m2
  • Low to moderate physically active (≤90 min of structured physical activity/week)

排除标准

  • Pregnancy
  • Glucose-lowering treatment
  • Treatment with steroids and other immunomodulating drugs
  • Contraindication to increased levels of physical activity
  • Liver disease (ALAT elevated more than 3 times above upper normal limit, or reduced levels of the liver function markers albumin and KF II+VII+X)
  • Renal insufficiency (eGFR\<60 ml/min)
  • Prior history of lactic acidosis
  • HbA1c \>55 mmol/mol and/or 2-hPG in the 75-g OGTT \> 15 mmol/L

研究组 & 干预措施

Metformin treatment

干预措施: Metformin treatment

Placebo treatment

干预措施: Placebo treatment

结局指标

主要结局

Difference in postprandial glycemic control as assessed by mean blood glucose concentration during a 4 hour mixed-meal tolerance test

时间窗: Day 17 (no acute exercise [control day]) and 24 (following an acute exercise bout)

次要结局

  • Difference in exogenous glucose uptake as assessed by rate of ingested glucose tracer appearance in blood(Day 17 (no acute exercise [control day]) and 24 (following an acute exercise bout))
  • Difference in endogenous glucose production as assessed by rate of infused glucose tracer appearance in blood(Day 17 (no acute exercise [control day]) and 24 (following an acute exercise bout))
  • Difference in peripheral glucose uptake as assessed by rate of glucose disappearance from blood(Day 17 (no acute exercise [control day]) and 24 (following an acute exercise bout))

研究点 (1)

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