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Phase 3 N=172 Randomized Triple-blind Treatment

Perimenopausal Estrogen Replacement Therapy Study

Perimenopause · Menopause · Depression

Enrolled (actual)
172
Serious AEs
0.0%
Results posted
Aug 2017
Primary outcome: Primary: Change in Depressive Symptoms as Indicated by The Center for Epidemiologic Studies Depression Scale (CES-D) — 1.04; -1.02 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Estradiol (Drug); Placebo (Drug)
Age
Adult · 45+ yrs
Sex
Female
Sponsor
University of North Carolina, Chapel Hill
Primary completion
Mar 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Depressive Symptoms as Indicated by The Center for Epidemiologic Studies Depression Scale (CES-D)
1.04; -1.02
PRIMARY
Change in Psychiatric Diagnosis as Assessed by the Structured Clinical Interview for DSM Disorders I/NP
PRIMARY
Change in Stress Reactivity During Laboratory Session Including Trier Social Stress Test
0.02; -0.18
SECONDARY
Change in Functional Well-being as Assessed by the Medical Outcomes Study 36-item Short Form (SF-36)
0.94; 2.32
SECONDARY
Percentage Meeting Criteria for Metabolic Risk [Baseline and Month 12]
17; 17; 10; 9
SECONDARY
Change in Percentage of Brachial Artery Diameter
-0.65; 0.56
SECONDARY
Change in Baroreceptor Sensitivity
0.19; 0.43

Summary

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.

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • currently taking antidepressant medication
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01308814). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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