The Estrogen Replacement and Atherosclerosis Trial ; Primary Outcome Measure is Mean Minimal Coronary Artery Diameter After Avg of 3.2 Yrs. (ERA)
Primary Purpose
Heart Disease
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
0.625 mg of conjugated equine estrogen
0.625 mg of conjugated equine estrogen plus 2.5 mg of medroxyprogesterone acetate
placebo tablets
Sponsored by
About this trial
This is an interventional prevention trial for Heart Disease
Eligibility Criteria
Inclusion Criteria:
- postmenopausal
- not currently receiving estrogen-replacement treatment
- one or more epicardial coronary stenoses of at least 30 percent of the luminal diameter, as measured by quantitative coronary angiography
Exclusion Criteria:
- known or suspected breast or endometrial carcinoma
- previous or planned coronary-artery bypass surgery,
- a history of deep-vein thrombosis or pulmonary embolism,
- symptomatic gallstones,
- serum aspartate aminotransferase level more than 1.5 times the normal value,
- fasting triglyceride level of more than 400 mg per deciliter
- serum creatinine level of more than 2.0 mg per deciliter
- more than 70 percent stenosis of the left main coronary artery,
- uncontrolled hypertension, or
- uncontrolled diabetes.
Sites / Locations
- Wake Forest University School of Medicine
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
unopposed estrogen
estrogen-plus-medroxyprogesterone
placebo
Arm Description
0.625 mg of conjugated equine estrogen
0.625 mg of conjugated equine estrogen plus 2.5 mg of medroxyprogesterone acetate
placebo
Outcomes
Primary Outcome Measures
mean minimal coronary-artery diameter
mean minimal coronary-artery diameter within each subject at follow-up, analyzed on an intention-to-treat basis
Secondary Outcome Measures
stenosis as a percentage of the reference diameter
development of new lesions in a patient
Models focusing on change in diameter were also examined
Full Information
NCT ID
NCT03097120
First Posted
April 26, 2011
Last Updated
May 19, 2023
Sponsor
Wake Forest University Health Sciences
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT03097120
Brief Title
The Estrogen Replacement and Atherosclerosis Trial ; Primary Outcome Measure is Mean Minimal Coronary Artery Diameter After Avg of 3.2 Yrs.
Acronym
ERA
Official Title
The Estrogen Replacement and Atherosclerosis Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
January 1995 (undefined)
Primary Completion Date
January 2001 (Actual)
Study Completion Date
January 2001 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Background: Heart disease is a major cause of illness and death in women. To understand better the role of estrogen in the treatment and prevention of heart disease, more information is needed about its effects on coronary atherosclerosis and the extent to which concomitant progestin therapy may modify these effects.
Methods: The investigators randomly assigned a total of 309 women with angiographically verified coronary disease to receive 0.625 mg of conjugated estrogen per day, 0.625 mg of conjugated estrogen plus 2.5 mg of medroxyprogesterone acetate per day, or placebo. The women were followed for a mean (±SD) of 3.2±0.6 years. Base-line and follow-up coronary angiograms were were analyzed by quantitative methods. Follow-up coronary angiograms were obtained after an average of 3.2 years of follow up.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Disease
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
309 (Actual)
8. Arms, Groups, and Interventions
Arm Title
unopposed estrogen
Arm Type
Active Comparator
Arm Description
0.625 mg of conjugated equine estrogen
Arm Title
estrogen-plus-medroxyprogesterone
Arm Type
Active Comparator
Arm Description
0.625 mg of conjugated equine estrogen plus 2.5 mg of medroxyprogesterone acetate
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Drug
Intervention Name(s)
0.625 mg of conjugated equine estrogen
Intervention Description
one tablet containing 0.625 mg of conjugated equine estrogen and a placebo tablet daily
Intervention Type
Drug
Intervention Name(s)
0.625 mg of conjugated equine estrogen plus 2.5 mg of medroxyprogesterone acetate
Intervention Description
one tablet of 0.625 mg of conjugated equine estrogen plus one tablet 2.5 mg of medroxyprogesterone acetate daily
Intervention Type
Drug
Intervention Name(s)
placebo tablets
Intervention Description
two placebo tablets daily
Primary Outcome Measure Information:
Title
mean minimal coronary-artery diameter
Description
mean minimal coronary-artery diameter within each subject at follow-up, analyzed on an intention-to-treat basis
Time Frame
at average of 3.2 years follow-up
Secondary Outcome Measure Information:
Title
stenosis as a percentage of the reference diameter
Time Frame
at average of 3.2 years follow-up
Title
development of new lesions in a patient
Time Frame
at average of 3.2 years follow-up
Title
Models focusing on change in diameter were also examined
Time Frame
at average of 3.2 years follow-up
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
postmenopausal
not currently receiving estrogen-replacement treatment
one or more epicardial coronary stenoses of at least 30 percent of the luminal diameter, as measured by quantitative coronary angiography
Exclusion Criteria:
known or suspected breast or endometrial carcinoma
previous or planned coronary-artery bypass surgery,
a history of deep-vein thrombosis or pulmonary embolism,
symptomatic gallstones,
serum aspartate aminotransferase level more than 1.5 times the normal value,
fasting triglyceride level of more than 400 mg per deciliter
serum creatinine level of more than 2.0 mg per deciliter
more than 70 percent stenosis of the left main coronary artery,
uncontrolled hypertension, or
uncontrolled diabetes.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David M. Herrington, MD, MHS
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wake Forest University School of Medicine
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
10822123
Citation
Herrington DM, Reboussin DM, Klein KP, Sharp PC, Shumaker SA, Snyder TE, Geisinger KR. The estrogen replacement and atherosclerosis (ERA) study: study design and baseline characteristics of the cohort. Control Clin Trials. 2000 Jun;21(3):257-85. doi: 10.1016/s0197-2456(00)00054-4. Erratum In: Control Clin Trials 2000 Aug;21(4):414.
Results Reference
background
PubMed Identifier
10954759
Citation
Herrington DM, Reboussin DM, Brosnihan KB, Sharp PC, Shumaker SA, Snyder TE, Furberg CD, Kowalchuk GJ, Stuckey TD, Rogers WJ, Givens DH, Waters D. Effects of estrogen replacement on the progression of coronary-artery atherosclerosis. N Engl J Med. 2000 Aug 24;343(8):522-9. doi: 10.1056/NEJM200008243430801.
Results Reference
result
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The Estrogen Replacement and Atherosclerosis Trial ; Primary Outcome Measure is Mean Minimal Coronary Artery Diameter After Avg of 3.2 Yrs.
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