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临床试验/NCT02339506
NCT02339506已完成不适用

Stress and the Nervous System

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2015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
不适用
状态
已完成
入组人数
23
试验地点
1
主要终点
Cardiovagal Baroreflex Sensitivity (Modified Oxford Technique)

研究概览

简要总结

Models of stress such as hypoglycemia have identified that stress results the next day in decreased baroreflex sensitivity. This project will test the hypothesis that these delayed changes in autonomic nervous system function are secondary to a rise in ACTH. The investigators will infuse cosyntropin versus placebo in a double-blind, crossover study in healthy adults and measure the delayed effects on the autonomic system as measured by cardiovagal baroreflex sensitivity.

详细描述

Stress has complex effects on the body's physiology. Models of stress such as hypoglycemia have identified that stress activates the hypothalamic-pituitary-adrenal (HPA) axis and sympathoadrenal system acutely. Additionally, there are delayed effects of prior exposure to hypoglycemia. The day after being exposed to a hypoglycemic stimulus there are: 1) decreases in the catecholamine release to a new hypoglycemic stress; 2) decreases in the muscle sympathetic nerve activity (MSNA) response to either a new hypoglycemic challenge or transient hypotension; 3) decreases in cardiac vagal baroreflex sensitivity (BRS); and 4) increases in sensitivity to thermal pain and altered temporal summation (decreased tolerance to a repeated minimally painful stimulus). This project will test the hypothesis that these delayed changes in autonomic nervous system function are secondary to a rise in ACTH that occurs in response to stress.

Primary Aim. Infusion of ACTH (cosyntropin) will lead the next day to decreased cardiovagal baroreflex sensitivity in healthy subjects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects must be currently healthy, BMI 18-32 kg/m2, and not be on any medications.
  • This study will recruit men and women. Due to concerns about estrogen's effects on hormone levels and possible contributions of menstrual symptoms on pain sensing thresholds, we will schedule the inpatient studies to avoid the early follicular phase in normally cycling women.
  • Subjects must have normal laboratory values for:
  • Complete blood count
  • Serum creatinine, sodium, potassium, glucose, liver enzymes
  • Urine pregnancy test (if female)

排除标准

  • We will exclude individuals with:
  • Systolic blood pressure > 140 or < 90 mm Hg
  • Diastolic blood pressure > 90 mm Hg
  • Creatinine clearance ≤ 60 mL/min, as calculated by MDRD formula
  • Known DM, CHF, CAD, PVD, CVA, MI, asthma
  • Known or history of Cushing's disease or adrenal insufficiency
  • Known neurologic disease
  • Known psychiatric disease
  • Steroid use (oral or inhaled, local or systemic injections, within the past 6 months)
  • Significant concomitant medical illnesses
  • Current excessive alcohol (>10oz ethanol/week)
  • Current use of recreational drugs
  • Current smokers
  • Current pregnancy
  • Chronic use of non-steroidal anti-inflammatory or narcotic medications
  • Evidence of ischemia or heart block on screening electrocardiogram (greater than type I-second degree heart block, left bundle branch block, or ST-T wave changes in 2 or more contiguous leads)
  • Subjects taking any prescription medications (other than oral birth control pills) or herbal medications will be excluded.

研究组 & 干预措施

Cosyntropin

Active Comparator

Subjects will receive cosyntropin infusion at 70 mcg/hr for two sessions of 2.5 hours each on day 2 of a three day admission to our research center.

干预措施: Cosyntropin (Drug)

Normal saline (Placebo)

Placebo Comparator

Subjects will receive normal saline infusion for two sessions of 2.5 hours each on day 2 of a three day admission to our research center.

干预措施: Placebo (Drug)

结局指标

主要结局

Cardiovagal Baroreflex Sensitivity (Modified Oxford Technique)

时间窗: Baseline, 4-hours after infusion, 24-hours after infusion

Cardiovagal baroreflex sensitivity will be measured with the Modified Oxford Technique before, during, and after drug infusions, to evaluate the effects of cosyntropin infusions.

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

Gail Kurr Adler

Associate Professor

Brigham and Women's Hospital

研究点 (1)

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