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临床试验/NCT01406015
NCT01406015已完成不适用

Mineralocorticoid Receptor and Obesity Induced Cardiovascular Complications

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2009年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
38
试验地点
1
主要终点
Change From Baseline in Post-ischemic Dilatation

研究概览

简要总结

The purpose of this study is to find out if spironolactone, a drug that blocks the action of aldosterone, can make the blood vessels work better in people with obesity. The investigators also want to find out whether spironolactone causes changes in levels of insulin and markers of inflammation.

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
Triple (Participant, Care Provider, Investigator)

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

  • Age 18-70 years
  • Good health as evidenced by history and physical exam
  • Body Mass Index (BMI): >30 kg/m2 and <45 kg/m2
  • Exclusion criteria:
  • Medical illnesses other than treated hypothyroidism
  • Blood Pressure (BP) >135/85 or systolic BP <90 mm Hg
  • Hepatic disease (transaminase > 3 times normal)
  • Renal impairment (Creatinine clearance <60 ml/min)
  • Baseline serum Potassium (K) >5.0 mmol/L
  • History of drug or alcohol abuse
  • Allergies to spironolactone
  • Participation in any other concurrent clinical trial
  • Women using oral contraceptives within the last 3 months

排除标准

  • 未提供

研究组 & 干预措施

Spironolactone

Active Comparator

干预措施: Spironolactone (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Change From Baseline in Post-ischemic Dilatation

时间窗: Baseline and Week 6

Ultrasonography of the brachial artery was performed to evaluate endothelial function by flow mediated dilatation (FMD) studies. A blood pressure cuff was placed on the participant's upper arm and was compressed for 5 minutes. After release of compression, brachial artery diameter and blood flow velocity were measured. FMD was expressed as the percentage change in brachial artery diameter. A positive change from Baseline indicates improvement.

次要结局

  • Change From Baseline in Para-aminohippurate (PAH) Clearance(Baseline and Week 6 (Prior to PAH infusion and at 50 and 60 minutes post PAH infusion))
  • Change From Baseline in Markers of Inflammation(Baseline and Week 6)
  • Change From Baseline in Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)(Baseline and Week 6 (Prior to ingesting glucose and every 30 minutes for 120 minutes))
  • Change From Baseline in Insulin Sensitivity Index (ISI)(Baseline and Week 6 (Prior to ingesting glucose and every 30 minutes for 120 minutes))

研究者

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

Rajesh K. Garg

Associate Physician

Brigham and Women's Hospital

研究点 (1)

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