Estrogen, HDL, and Coronary Heart Disease in Women
Cardiovascular Diseases, Coronary Disease, Heart Diseases
About this trial
This is an interventional health services research trial for Cardiovascular Diseases
Eligibility Criteria
Inclusion criteria: age >55 years without natural menses for at least 5 years or a serum FSH levels >40 IU/L without natural menses for at least 1 y or bilateral oophorectomy documented coronary artery disease Exclusion criteria: history of breast or endometrial carcinoma history of deep-vein thrombosis or pulmonary embolism previous or planned coronary bypass gallstones fasting TG levels >400 mg/dl uncontrolled diabetes uncontrolled hypertension serum creatinine >2 mg/dl a >70% stenosis of the left main coronary artery.
Sites / Locations
- HNRCA at Tufts University
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Experimental
Experimental
Sugar Pill
Estrogens, Conjugated (USP)
Medroxyprogesterone 17-acetate
Placebo
Conjugated Equine Estrogen 0.625 mg/day for 3 years, drug
Conjugated Equine Estrogen 0.625 mg/day plus Medroxyprogesterone Acetate 2.5 mg/day