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EPAT: Estrogen in the Prevention of Atherosclerosis Trial

Primary Purpose

Atherosclerosis, Postmenopause

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Micronized 17B-estradiol
Sponsored by
National Institute on Aging (NIA)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Atherosclerosis focused on measuring cardiovascular disease, CVD, estrogen, cholesterol, LDL, lipids, postmenopausal

Eligibility Criteria

46 Years - 80 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Postmenopausal female (serum estradiol less than 20 pg/ml) 46 to 80 years old Fasting LDL-C levels 130 to 210 mg/dL Triglyceride levels less than 400 mg/dL Current non-smoker Exclusion Criteria: Clinical evidence of cardiovascular disease HDL-C level less than 30 mg/dL Fasting blood glucose greater than 200 mg/dL Previous hormonal replacement therapy (non-contraceptive) over 10 years duration and/or current use within 1 month Uncontrolled hypertension Untreated thyroid disease Renal insufficiency Clinical evidence of congestive heart failure Life threatening disease with prognosis less than 5 years Alcohol intake greater than 5 drinks per day (1 drink = 1 1/2 oz distilled spirits, 4 oz wine, or 12 oz beer) or substance abuse (intravenous drug abuse, cocaine use) History of estrogen dependent cancer or detected at screening or any other disorder precluding use of ERT Hot flashes greater than 5 per day which interfere with daily activity and preclude randomization to placebo.

Sites / Locations

  • Atherosclerosis Research Unit, Division of Cardiovascular Medicine, Department of Medicine

Outcomes

Primary Outcome Measures

rate of change of distal common carotid artery (CCA) far wall intima-media thickness (IMT)

Secondary Outcome Measures

lipid and non-lipid factors

Full Information

First Posted
June 20, 2005
Last Updated
December 9, 2009
Sponsor
National Institute on Aging (NIA)
Collaborators
Mead Johnson Nutrition
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1. Study Identification

Unique Protocol Identification Number
NCT00115024
Brief Title
EPAT: Estrogen in the Prevention of Atherosclerosis Trial
Official Title
Estrogen in the Prevention of Atherosclerosis Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2005
Overall Recruitment Status
Completed
Study Start Date
April 1994 (undefined)
Primary Completion Date
November 1998 (Actual)
Study Completion Date
November 1998 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute on Aging (NIA)
Collaborators
Mead Johnson Nutrition

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine the effects of estrogen replacement therapy (ERT) on the progression of early atherosclerosis in healthy postmenopausal women without preexisting cardiovascular disease (CVD).
Detailed Description
The primary goal of this randomized, controlled trial is to determine if ERT stabilizes, retards, and/or reverses the progression of atherosclerosis in postmenopausal women. We will further evaluate the association of lipid and non-lipid factors of ERT-mediated reduction in the progression of early atherosclerosis. Ultrasonography will be used to measure the rate of change in the thickness of the carotid artery. Blood samples will be used for measuring lipid and non-lipid mediators of ERT. A total of 222 healthy postmenopausal women 46 to 80 years old without CVD symptoms will be randomized to receive either micronized 17B-estradiol (Estrace) 1mg/day, or a matching placebo tablet daily. All women will be on a low fat/low cholesterol diet, and will receive pravastatin if their LDL cholesterol level exceeds 160 mg/dL. Participants will undergo ultrasonography at baseline and every 6 months throughout the 2 years of randomized treatment. Measurements of lipid and non-lipid biochemical markers will also be done at baseline and every 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerosis, Postmenopause
Keywords
cardiovascular disease, CVD, estrogen, cholesterol, LDL, lipids, postmenopausal

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
222 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Micronized 17B-estradiol
Primary Outcome Measure Information:
Title
rate of change of distal common carotid artery (CCA) far wall intima-media thickness (IMT)
Secondary Outcome Measure Information:
Title
lipid and non-lipid factors

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
46 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Postmenopausal female (serum estradiol less than 20 pg/ml) 46 to 80 years old Fasting LDL-C levels 130 to 210 mg/dL Triglyceride levels less than 400 mg/dL Current non-smoker Exclusion Criteria: Clinical evidence of cardiovascular disease HDL-C level less than 30 mg/dL Fasting blood glucose greater than 200 mg/dL Previous hormonal replacement therapy (non-contraceptive) over 10 years duration and/or current use within 1 month Uncontrolled hypertension Untreated thyroid disease Renal insufficiency Clinical evidence of congestive heart failure Life threatening disease with prognosis less than 5 years Alcohol intake greater than 5 drinks per day (1 drink = 1 1/2 oz distilled spirits, 4 oz wine, or 12 oz beer) or substance abuse (intravenous drug abuse, cocaine use) History of estrogen dependent cancer or detected at screening or any other disorder precluding use of ERT Hot flashes greater than 5 per day which interfere with daily activity and preclude randomization to placebo.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Howard N. Hodis, MD
Organizational Affiliation
University of Southern California, Atherosclerosis Research Unit, Division of Cardiovascular Medicine, Department of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Atherosclerosis Research Unit, Division of Cardiovascular Medicine, Department of Medicine
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11730394
Citation
Hodis HN, Mack WJ, Lobo RA, Shoupe D, Sevanian A, Mahrer PR, Selzer RH, Liu Cr CR, Liu Ch CH, Azen SP; Estrogen in the Prevention of Atherosclerosis Trial Research Group. Estrogen in the prevention of atherosclerosis. A randomized, double-blind, placebo-controlled trial. Ann Intern Med. 2001 Dec 4;135(11):939-53. doi: 10.7326/0003-4819-135-11-200112040-00005.
Results Reference
result
PubMed Identifier
17329508
Citation
Steiner AZ, Xiang M, Mack WJ, Shoupe D, Felix JC, Lobo RA, Hodis HN. Unopposed estradiol therapy in postmenopausal women: results from two randomized trials. Obstet Gynecol. 2007 Mar;109(3):581-7. doi: 10.1097/01.AOG.0000251518.56369.eb.
Results Reference
derived

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EPAT: Estrogen in the Prevention of Atherosclerosis Trial

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