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临床试验/NCT00732160
NCT00732160已完成不适用

Aldosterone and Glucose Homeostasis

Vanderbilt University1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2008年9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
34
试验地点
1
主要终点
Insulin Secretion

研究概览

简要总结

Determine the effect of aldosterone on how the body handles glucose (sugar).

详细描述

Determine the effect of aldosterone on glucose metabolism in humans.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ambulatory subjects, 18 to 70 years of age, inclusive
  • For female subjects, the following conditions must be met:
  • a postmenopausal status for at least 1 year, or b status-post surgical sterilization, or c if of childbearing potential, utilization of adequate birth control and willingness to undergo urine beta-hcg testing prior to drug treatment and on every study day
  • Metabolic Syndrome as defined by the presence of > 3 of the following:
  • a Systolic Blood Pressure > 130 mm Hg OR Diastolic Blood Pressure > 85 mm Hg. b Glucose Intolerance (Fasting Plasma Glucose > 100 mg/dL) c Increased triglyceride level > 150mg/dL (1.7mmol/L) d Decreased levels of HDL cholesterol For males, less than 40 mg/dL For females, less than 50 mg/dL e Waist circumference For males, greater than 40 inches (102 cm) For females, greater than 35 inches (89 cm).

排除标准

  • Previously diagnosed Type I Diabetes , or the use of anti-diabetic medication. Subjects with type II diabetes not on medication will be allowed to participate if fasting blood glucose is <200mg/dL.
  • Prior allergies to medications used in the study protocol (e.g. L-arginine, potassium chloride).
  • Screening plasma potassium <3.5 mmol/L or use of chronic potassium supplements for the treatment of hypokalemia
  • Use of hormone replacement therapy
  • If on statin therapy for hypercholesterolemia, a change in dose within the past 6 months.
  • Breast-feeding
  • Cardiovascular disease such as prior myocardial infarction, presence of angina pectoris, significant arrhythmia, congestive heart failure (LV hypertrophy acceptable), deep vein thrombosis, pulmonary embolism, second or third degree heart block, mitral valve stenosis, aortic stenosis or hypertrophic cardiomyopathy
  • Treatment with anticoagulants
  • History of serious neurologic disease such as cerebral hemorrhage, stroke, seizure, or transient ischemic attack
  • History or presence of immunological or hematological disorders
  • Diagnosis of asthma requiring use of inhaled beta agonist >1 time per week
  • Clinically significant gastrointestinal impairment that could interfere with drug absorption
  • Impaired hepatic function [aspartate amino transaminase (AST) and/or alanine amino transaminase (ALT) >2.0 x upper limit of normal range]
  • Impaired renal function [estimated glomerular filtration rate (eGFR) of <60ml/min] as determined by the four-variable Modification of Diet in Renal Disease (MDRD) equation, where serum creatinine (Scr) is expressed in mg/dl and age in years:
  • eGFR <60 ml/min
  • Hematocrit <35%
  • Any underlying or acute disease requiring regular medication which could possibly pose a threat to the subject or make implementation of the protocol or interpretation of the study results difficult, such as arthritis treated with non-steroidal antiinflammatory drugs
  • Treatment with chronic systemic glucocorticoid therapy (more than 7 consecutive days in 1 month)
  • Treatment with lithium salts
  • History of alcohol or drug abuse
  • Treatment with any investigational drug in the 1 month preceding the study
  • Mental conditions rendering the subject unable to understand the nature, scope and possible consequences of the study
  • Inability to comply with the protocol, e.g., uncooperative attitude, inability to return for follow-up visits, and unlikelihood of completing the study

研究组 & 干预措施

HS-V/A; LS-V/A

Experimental

High Sodium diet- Vehicle infusion then Aldosterone infusion Low Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: Vehicle Infusion (V) (Drug)

HS-V/A; LS-V/A

Experimental

High Sodium diet- Vehicle infusion then Aldosterone infusion Low Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: Aldosterone infusion (A) (Drug)

HS-V/A; LS-V/A

Experimental

High Sodium diet- Vehicle infusion then Aldosterone infusion Low Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: High Sodium Diet (HS) (Other)

HS-V/A; LS-V/A

Experimental

High Sodium diet- Vehicle infusion then Aldosterone infusion Low Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: Low Sodium Diet (LS) (Other)

HS-A/V; LS-A/V

Experimental

High Sodium diet- Aldosterone infusion then Vehicle infusion Low Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: Aldosterone infusion (A) (Drug)

HS-A/V; LS-A/V

Experimental

High Sodium diet- Aldosterone infusion then Vehicle infusion Low Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: Vehicle Infusion (V) (Drug)

HS-A/V; LS-A/V

Experimental

High Sodium diet- Aldosterone infusion then Vehicle infusion Low Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: High Sodium Diet (HS) (Other)

HS-A/V; LS-A/V

Experimental

High Sodium diet- Aldosterone infusion then Vehicle infusion Low Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: Low Sodium Diet (LS) (Other)

LS-V/A; HS-V/A

Experimental

Low Sodium diet- Vehicle infusion then Aldosterone infusion High Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: Aldosterone infusion (A) (Drug)

LS-V/A; HS-V/A

Experimental

Low Sodium diet- Vehicle infusion then Aldosterone infusion High Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: Vehicle Infusion (V) (Drug)

LS-V/A; HS-V/A

Experimental

Low Sodium diet- Vehicle infusion then Aldosterone infusion High Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: High Sodium Diet (HS) (Other)

LS-V/A; HS-V/A

Experimental

Low Sodium diet- Vehicle infusion then Aldosterone infusion High Sodium diet- Vehicle infusion then Aldosterone infusion

干预措施: Low Sodium Diet (LS) (Other)

LS-A/V; HS-A/V

Experimental

Low Sodium diet- Aldosterone infusion then Vehicle infusion High Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: Aldosterone infusion (A) (Drug)

LS-A/V; HS-A/V

Experimental

Low Sodium diet- Aldosterone infusion then Vehicle infusion High Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: Vehicle Infusion (V) (Drug)

LS-A/V; HS-A/V

Experimental

Low Sodium diet- Aldosterone infusion then Vehicle infusion High Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: High Sodium Diet (HS) (Other)

LS-A/V; HS-A/V

Experimental

Low Sodium diet- Aldosterone infusion then Vehicle infusion High Sodium diet- Aldosterone infusion then Vehicle infusion

干预措施: Low Sodium Diet (LS) (Other)

结局指标

主要结局

Insulin Secretion

时间窗: 3 hours

Acute Insulin response during Hyperglycemic clamp (delta insulin uU/mL, t=0-10)

次要结局

  • Insulin Sensitivity(3 hours)

研究者

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

James Matt Luther

Assistant Professor of Medicine

Vanderbilt University

研究点 (1)

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