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临床试验/NCT00759291
NCT00759291已完成2 期

The Impact of Free Fatty Acid Reduction on Vascular Function in the Metabolic Syndrome

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2006年4月1日最近更新:
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
40
试验地点
1
主要终点
Flow Mediated Vasodilation

研究概览

简要总结

This study will test the hypothesis that reducing the release of free fatty acids (FFA) from fat cells will restore insulin-mediated, endothelium-dependent vasodilation in people with the metabolic syndrome.

详细描述

We hypothesize that acipimox, by decreasing plasma FFA concentrations, will augment endothelium-dependent vasodilation in conduit vessels and insulin-mediated vasodilation in forearm resistance arterioles in vivo, whole-body insulin sensitivity, and AKT (also known as Protein Kinase B) and endothelial nitric oxide synthase (eNOS) phosphorylation in skin biopsy specimens ex vivo, when compared with placebo.

研究设计

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

入排标准

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

入选标准

  • Adults with metabolic syndrome, defined as the presence of 3 of 5 components of the syndrome as defined by the National Cholesterol Education Program including:
  • abdominal obesity
  • elevated fasting blood sugar (110 mg/dL< glucose < 126 mg/dL)
  • elevated fasting blood triglycerides (> 150 mg/dL)
  • hypertension (BP > 140/90 mm HG)
  • Normal cardiovascular examination

排除标准

  • Diabetes mellitus
  • Untreated hypercholesterolemia (LDL > 75th percentile for age)
  • Cigarette smoking within 1 year
  • Renal insufficiency (creatinine > 1.4 mg/dl)
  • Blood dyscrasia
  • Hepatic dysfunction (ALT > 2x normal)
  • Evident coronary/peripheral atherosclerosis

研究组 & 干预措施

Acipimox

Active Comparator

Acipimox treatment QID for 7 days

干预措施: acipimox (Drug)

Placebo

Placebo Comparator

Placebo treatment QID for 7 days

干预措施: Placebo (Drug)

结局指标

主要结局

Flow Mediated Vasodilation

时间窗: After 7 days of each treatment.

Brachial artery response to a 5 minute blood pressure cuff-applied ischemic period

次要结局

未报告次要终点

研究者

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

Joshua A. Beckman, MD

Associate Professor of Medicine, Harvard Medical School

Brigham and Women's Hospital

研究点 (1)

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