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临床试验/NCT02269072
NCT02269072撤回不适用

Testosterone Regulation of the Natriuretic Peptide System

Massachusetts General Hospital0 个研究点开始时间: 2015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
撤回
主要终点
Atrial natriuretic peptide levels

研究概览

简要总结

The proposed study is a physiologic investigation of the effects of testosterone on the natriuretic peptide system. The hypotheses of the study are that testosterone administration will decrease natriuretic peptide levels and salt excretion. The entire protocol is 8 weeks in duration.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Men: aged 18 to 40 years, normal testosterone and free testosterone levels, no history of hypertension, and BMI between 18.5 and
  • Women: aged 18 to 40 years old, regular menstrual periods, negative pregnancy test, no oral contraceptives for ≥ 3 mos, no history of hypertension, BMI between 18.5 and 25.

排除标准

  • Antihypertensives, diuretics or insulin, diabetes mellitus, prior cardiovascular, abnormal liver or renal disease, history of cancer, atrial fibrillation, or abnormal sodium or potassium level.

研究组 & 干预措施

Testosterone

Active Comparator

Testosterone cream applied daily

干预措施: Nesiritide (Drug)

Testosterone

Active Comparator

Testosterone cream applied daily

干预措施: Testosterone (Drug)

Testosterone

Active Comparator

Testosterone cream applied daily

干预措施: Leuprolide (Drug)

Testosterone

Active Comparator

Testosterone cream applied daily

干预措施: Anastrozole (Drug)

Placebo

Placebo Comparator

Identical placebo cream applied daily

干预措施: Nesiritide (Drug)

Placebo

Placebo Comparator

Identical placebo cream applied daily

干预措施: Leuprolide (Drug)

Placebo

Placebo Comparator

Identical placebo cream applied daily

干预措施: Anastrozole (Drug)

Placebo

Placebo Comparator

Identical placebo cream applied daily

干预措施: Placebo (Drug)

结局指标

主要结局

Atrial natriuretic peptide levels

时间窗: 8 weeks

次要结局

  • Urinary salt excretion(8 weeks)

研究者

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

Karen Klahr Miller, MD

Director, Neuroendocrine Research Program in Women's Health

Massachusetts General Hospital

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