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临床试验/NCT00608465
NCT00608465终止4 期

Defining Strategies for Improving Endothelial and Fibrinolytic Dysfunction in Obesity

Vanderbilt University1 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2006年5月最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
终止
入组人数
4
试验地点
1
主要终点
This Study Will Analyze Patients' Genetic Make up to Identify Who May be at Greater Risk for Heart Disease and Strokes in Relationship to High Blood Pressure and Central Obesity.

研究概览

简要总结

The combination of high blood pressure and having central obesity is an increasing important factor for heart disease in men and women. It can also lead to the early development of hardening of the arteries and increased risk of a stroke. This study will analyze patients' genetic make up to identify who may be at greater risk for heart disease and strokes in relationship to high blood pressure and central obesity.

详细描述

Obesity is an increasingly important risk factor for cardiovascular disease in men and women and is associated with the premature development of atherosclerosis, and increased risk of stroke. A classical perspective of cardiovascular risk does not adequately explain all of the cardiovascular events associated with obesity. Elevated plasma levels of plasminogen activator inhibitor type I (PAI-1) are one of the biochemical hallmarks for obesity and likely contribute the increased risk of atherothrombotic events in patients with obesity. The central hypothesis of this proposal is that the increased risk of atherothrombotic events in patients with obesity. The central hypothesis of this proposal is that vascular PAI-1 excess promotes the development of intravascular thrombosis. We will test the hypothesis that secreted factors from adipocytes have autocrine, paracrine and endocrine effects that have a deleterious effect on the fibrinolytic system, either by enhancing PAI-1 production or impairing endothelial t-PA release. From a public health perspective, there is no greater threat to America's cardiovascular health than the epidemic of obesity. It is anticipated that this study will provide new insights nto the molecular mechanisms that contribute to the development of fibrinolytic dysfunction and cardiovascular disease in obesity.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

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

  • Male or females between the ages of 18 to 65 years of age.
  • Documented diagnosis for the metabolic syndrome:
  • Subjects with hypertension (SP>130mmHg)
  • Subjects with central obesity (females waist >35"; males waist >40")
  • Subjects with dyslipidemia (HDL <40mg/dl, triglycerides > 150 mg/dl)
  • Subjects who are insulin resistance (fasting glucose >100mg/dl)

排除标准

  • Subjects who smoke
  • Women who are pregnant (confirmed by urine beta-HCG).
  • Women who are breast feeding
  • Subjects with documentation of the following health risk:
  • Subjects with serum creatinine >2.0 mg/dl (males), >1.8 mg/dl (females)
  • Subjects whose creatinine clearance < 50 mls/min
  • Subjects with serum potassium >5.5mEql
  • Subjects with Type 2 diabetes with microalbuminuria (spot urine protein/creatinine ration >0.2)
  • Subjects who are currently taking the following medications:

研究组 & 干预措施

Treatment B

Active Comparator

Ramipril

干预措施: Ramipril (Drug)

Treatment A

Active Comparator

Eplerenone (study drug)

干预措施: Eplerenone (Drug)

结局指标

主要结局

This Study Will Analyze Patients' Genetic Make up to Identify Who May be at Greater Risk for Heart Disease and Strokes in Relationship to High Blood Pressure and Central Obesity.

时间窗: 10-weeks

Secreted Factors From Adipocytes Have Autocrine, Paracrine and Endocrine Effects That Have a Deleterious Effect on the Fibrinolytic System, Either by Enhancing PAI-1 Production or Impairing Endothelial t-PA Release

时间窗: 10-Week 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

James Muldowney

Assistant Professor of Medicine

Vanderbilt University

研究点 (1)

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