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临床试验/NCT00153166
NCT00153166已完成2 期

The Contribution of Inflammation and Insulin Resistance to Intermittent Claudication

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2004年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
76
试验地点
1
主要终点
Lower Extremity Skeletal Muscle Glucose Uptake

研究概览

简要总结

This trial will test the hypothesis that inflammation and insulin resistance contribute to reduced walking distance in subjects with intermittent claudication by impairing vascular reactivity and skeletal muscle metabolic function.

详细描述

People with peripheral arterial disease (PAD), an important clinical manifestation of atherosclerosis, often suffer symptoms of intermittent claudication that impair their walking ability and adversely affect their quality of life. People with PAD are also at increased risk for adverse cardiovascular events, including myocardial infarction, stroke and death. Unfortunately, medical therapies directed to the functional and limb-threatening manifestations are limited. Little attention has been paid to the biologic processes that cause PAD, and to atherogenic mechanisms that may preferentially affect the peripheral circulation.

Vascular inflammation and insulin resistance are two important and interdependent conditions that are associated with atherosclerosis. Subjects in this trial (160 adults with stable intermittent claudication who are not taking insulin or insulin-sensitizing medications, such as thiazolidinediones) will be randomized in a placebo-controlled, parallel design manner, to atorvastatin 80 mg orally daily (to reduce inflammation) and pioglitazone 45 mg orally once daily (to improve insulin sensitivity). Forty healthy adult subjects, age and gender-matched to a subset of the study group, will be enrolled to serve as a control population. Primary and secondary study endpoints include: treadmill walking time, endothelium-dependent vasodilation, and insulin-mediated skeletal muscle glucose uptake.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • symptomatic intermittent claudication for >= 6 months
  • resting ankle/brachial index (ABI) <=0.90
  • maximal treadmill walking time between 1-20 minutes
  • >= 20% decrease in ABI post treadmill exercise
  • 4 week statin wash-out prior to initial study testing (if applicable)

排除标准

  • myocardial infarction or coronary artery bypass surgery within past 6 months
  • lower extremity revascularization (surgical or percutaneous) within past 6 months
  • transient ischemic attack or ischemic stroke within past 6 months
  • pregnancy
  • uncontrolled hypertension (systolic pressure > 180mmHg and/or diastolic pressure > 100mmHg
  • serum creatinine >2.5
  • hepatic transaminases (AST, ALT) > 3x upper limit of normal (ULN)
  • creatine kinase > 5x ULN
  • known hypersensitivity to HMG-CoA reductase inhibitors
  • insulin dependent Type 2 diabetes
  • current treatment with thiazolidinedione

研究组 & 干预措施

Patients with PAD (Including diabetics)

Experimental

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: atorvastatin and pioglitazone (Drug)

Patients with PAD (Including diabetics)

Experimental

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: atorvastatin/placebo (Drug)

Patients with PAD (Including diabetics)

Experimental

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: pioglitazone/placebo (Drug)

Patients with PAD (Including diabetics)

Experimental

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: placebo/placebo (Drug)

PAD (Excluding Diabetics)

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: atorvastatin and pioglitazone (Drug)

PAD (Excluding Diabetics)

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: atorvastatin/placebo (Drug)

PAD (Excluding Diabetics)

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: pioglitazone/placebo (Drug)

PAD (Excluding Diabetics)

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: placebo/placebo (Drug)

Healthy Controls

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: atorvastatin and pioglitazone (Drug)

Healthy Controls

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: atorvastatin/placebo (Drug)

Healthy Controls

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: pioglitazone/placebo (Drug)

Healthy Controls

Active Comparator

Randomized to either atorvastatin and pioglitazone, atorvastatin/placebo, pioglitazone/placebo, or placebo/placebo.

干预措施: placebo/placebo (Drug)

结局指标

主要结局

Lower Extremity Skeletal Muscle Glucose Uptake

时间窗: 60 minutes

Net calf skeletal muscle glucose uptake determined by Patlak modeling.

次要结局

  • 'M' = Whole Body Insulin Sensitivity(every 5 minutes for 20 minutes)

研究者

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

Mark Alan Creager, MD

Principal Investigator

Brigham and Women's Hospital

研究点 (1)

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