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临床试验/NCT00694733
NCT00694733进行中(未招募)不适用

Regulation of Cortisol Metabolism and Fat Patterning

Oregon Health and Science University1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2005年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
140
试验地点
1
主要终点
To measure 24-hour CPR, free cortisol, and cortisol binding globulin levels in plasma; HSD 1 activity, glucocorticoid receptor binding, and cortisol levels in adipocytes; and urinary excretion of cortisol, cortisone and their metabolites.

研究概览

简要总结

The purpose of this study is to determine if estrogen or testosterone can affect cortisol levels and where fat builds up in our bodies.

详细描述

Subjects will be studied 3 or 4 times on the inpatient unit of the Oregon Clinical and Translational Research Center. During each visit, testing will include measuring the amount of whole body fat and fat in the stomach area, muscle, and liver; levels of cortisol in the blood, urine, and fat tissue (taken from a biopsy); how well insulin works (insulin sensitivity).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 62 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 40 postmenopausal women (age 40-62) and 30 men (age 18-45) will be recruited if they are healthy, at their lifetime maximal weight, have been weight stable for at least six months prior to entry, have a BMI between 19 and 39.9 kg/m2, and be willing to commit to not making significant changes to their diet or daily activities while enrolled in the study.

排除标准

  • Subjects will be excluded for potential confounders on body weight, cortisol production rates, sex steroid metabolism, or contraindications to strong magnetic fields:
  • Age less than 18 to exclude those who might be experiencing alterations in cortisol production or weight as a result of adolescent growth
  • Subjects who exercise > 30 minutes/day, 3 times a week
  • Heavy alcohol drinkers (> 2 drinks/ day)
  • Subjects with medical diagnosis including diabetes, heart disease, and cancer
  • Subjects with psychiatric illness (i.e., depression, psychosis, bipolar, schizophrenia; or are taking medications for these disorders)
  • BMI 40 kg/m2, since obesity influences levels of sex steroids and sex hormone binding globulin; or body weight > 136 kg (300 lbs), since this is the weight limit for the DEXA and MR machines
  • Presence of metal in the body such as body piercing, shrapnel, cardiac pacemakers or aneurysm clips
  • Endocrine diseases affecting body composition, such as untreated hypothyroidism or Cushing's syndrome, will be excluded by history and physical examination, or by laboratory evaluation if necessary.
  • Women with a contraindication to estrogen use will also be excluded, including: an estrogen dependent malignancy, active thrombophlebitis, history of deep venous thrombosis, hypertriglyceridemia, untreated hypertension, cardiovascular disease, migraine headaches, or current tobacco use.
  • Women with frequent hot flashes or disrupted sleep will also be excluded since they will be unlikely to tolerate randomization to placebo and continued symptoms and altered sleep cycles will independently affect cortisol secretion patterns.
  • All volunteers will have had a normal mammogram within the previous 12 months.
  • Any subject with previously unevaluated postmenopausal bleeding will not be included and, instead, will be referred to a physician for evaluation.
  • Women who underwent surgical menopause (bilateral ovariectomy) must be at least one year out from their surgery before considered eligible so as to allow weight stabilization after the procedure.
  • Men will have had a prostate exam by their primary health provider within the previous year or by the PI at the time of screening for this study.
  • Any subjects taking a blood thinning medication or with an abnormal exam will not be included and, instead, will be referred to a physician for evaluation

研究组 & 干预措施

1

Placebo Comparator

Men on placebo injections for 4 months

干预措施: Placebo injection (Drug)

2

Active Comparator

Men who receive Depo Lupron for 4 months, then are replaced with testosterone and aromatase inhibitor for 4 months.

干预措施: Depo Lupron/Aromatase inhibitor (Drug)

3

Active Comparator

Men who receive Depo Lupron for 4 months, then are replaced with testosterone and placebo for 4 months.

干预措施: Depo Lupron/placebo (Drug)

4

Placebo Comparator

Women on placebo cream

干预措施: placebo (Drug)

5

Active Comparator

Women on estrogen cream

干预措施: Estrogen cream (Drug)

结局指标

主要结局

To measure 24-hour CPR, free cortisol, and cortisol binding globulin levels in plasma; HSD 1 activity, glucocorticoid receptor binding, and cortisol levels in adipocytes; and urinary excretion of cortisol, cortisone and their metabolites.

时间窗: Before and after hormone replacement therapy

次要结局

  • To measure intramyocellular fat and intrahepatic fat by MRS, visceral and subcutaneous abdominal fat by CT scan, body composition (fat mass, lean mass, and bone mass) by DXA, and insulin sensitivity.(Before and after hormone replacement therapy)

研究者

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

Jonathan Purnell

Principal Investigator

Oregon Health and Science University

研究点 (1)

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