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临床试验/NCT01308814
NCT01308814已完成2 期

Depression, Estrogen Replacement, and Cardiovascular Health in the Perimenopause

University of North Carolina, Chapel Hill1 个研究点 分布在 1 个国家目标入组 172 人开始时间: 2010年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
172
试验地点
1
主要终点
Change in Psychiatric Diagnosis as Assessed by the Structured Clinical Interview for DSM Disorders I/NP

研究概览

简要总结

Study Background and Objectives: In the U.S. the majority of heart disease deaths are in women, not men. Much of the gender disparity in CVD rates relate to the burden of CV risk in women after the menopause. Depression has been associated with an increased risk for CVD morbidity and mortality. Even histories of recurrent depression in euthymic individuals are associated with elevated CV risk. Understanding the depression-CVD link may have particular relevance for women since women experience depression at a rate twice that of men. Substantial convergent evidence indicates that ovarian failure (estrogen deprivation) is one likely mechanism contributing to both CVD and depression in women. The perimenopause, a time associated with a two-fold increase in rates of depression, may provide an ideal opportunity for studying the pathophysiology of CV risk and depression in women.

The primary objective of this study is to examine the prophylactic role of estradiol in the development of depressive symptoms and the progression of cardiovascular risk in perimenopausal women with or without histories of depression. The investigators predict that women susceptible to depression will be particularly vulnerable to the acceleration of CVD in the context of the perimenopause and, consequently, will show differentially greater benefit of estradiol treatment during the menopause transition for both indices of CV risk (e.g. inflammation, endothelial function, stress reactivity), as well as depressive symptoms.

研究设计

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

入排标准

年龄范围
45 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • must be between 45 and 60 years of age
  • must be in the menopause transition (irregular/ absent menstrual cycles or hot flashes)
  • must be are medically healthy

排除标准

  • currently taking antidepressant medication

研究组 & 干预措施

Placebo

Placebo Comparator

Placebo patches for 12 months and placebo pills for 12 days every 2 months.

干预措施: Placebo (Drug)

Estradiol

Experimental

Transdermal 17β-estradiol (100 ug/day) for 12 months and oral micronized progesterone (200 mg/day) for 12 days every two months.

干预措施: Estradiol (Drug)

结局指标

主要结局

Change in Psychiatric Diagnosis as Assessed by the Structured Clinical Interview for DSM Disorders I/NP

时间窗: Baseline and when prompted by CES-D score

Change in Depressive Symptoms as Indicated by The Center for Epidemiologic Studies Depression Scale (CES-D)

时间窗: Baseline, month 12

Change from pre-trial (baseline) to post-trial (month 12) in the Center for Epidemiologic Studies Depression Scale (CES-D). The CES-D has a Range from 0-60, with higher scores indicating the presence of more symptomatology. A score of 16 or greater is indicative of clinically significant symptoms of depression.

Change in Stress Reactivity During Laboratory Session Including Trier Social Stress Test

时间窗: Baseline, month 12

Primary measures reflecting stress reactivity will consist of mean arterial pressure (MAP), vascular resistance index (VRI), plasma cortisol, and plasma IL-6. For each of these four measures, a delta score (change from rest to stress) will be calculated and then standardized as Z scores. The individual Z scores will then be averaged to yield a single Stress Reactivity profile measure (average z score) - a composite Z score reflecting magnitude of activation in the four primary stress-responsive pathways. This composite z score at baseline will be subtracted from the composite z score at 12 months to yield this outcome measure.

次要结局

  • Change in Functional Well-being as Assessed by the Medical Outcomes Study 36-item Short Form (SF-36)(Baseline, month 12)
  • Percentage Meeting Criteria for Metabolic Risk [Baseline and Month 12](Baseline, month 12)
  • Change in Percentage of Brachial Artery Diameter(Baseline, month 12)
  • Change in Baroreceptor Sensitivity(Baseline, month 12)

研究者

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

Susan Girdler, PhD

Principal Investigator

University of North Carolina, Chapel Hill

研究点 (1)

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