Oral Contraceptives in the Metabolic Syndrome
Metabolic Syndrome X, Insulin Resistance, Obesity
About this trial
This is an interventional prevention trial for Metabolic Syndrome X focused on measuring Inflammatory markers, oral contraceptions, obesity, metabolic syndrome X
Eligibility Criteria
Inclusion Criteria: Acceptable health based on interview, medical history, physical examination, and laboratory tests (comprehensive metabolic panel - SMA20, and complete blood count - CBC); Have not taken oral contraceptives (OCs) in the past 3 months; Ability to comply with the requirements of the study; Ability and willingness to provide signed, witnessed informed consent. In addition, women with the metabolic syndrome must meet the National Cholesterol Education Program (NCEP) defined criteria of the metabolic syndrome, that is, having at least 3 of the 5 factors: increased waist circumference > 35 inches, hypertriglyceridemia ≥ 150 mg/dL, low high-density lipoprotein (HDL) cholesterol < 50 mg/dL in women, hypertension (≥ 130/≥ 85 mmHg), fasting glucose ≥ 100 mg/dL. Obese women with or without the metabolic syndrome should have a Body Mass Index (BMI) > 30 kg/m2 and lean women should have a Body Mass Index BMI < 25 kg/m2. Exclusion Criteria: Diabetes mellitus by fasting glucose or a 2-hour oral glucose tolerance test (OGTT); Clinically significant pulmonary, cardiac (including but not limited to ischemic heart disease, stable/unstable angina, and congestive heart failure), renal, hepatic, cholestatic, neurologic, psychiatric, infectious, and malignant disease (other than melanoma skin cancer); History of thromboembolism, myocardial infarction, cerebrovascular accident, vascular disease, known coagulopathy, prolonged immobilization, or recent major surgery (within past 6 months); Systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 100 mmHg (mild hypertension is not an exclusion criterion); History of breast cancer, migraine headaches, or age ≥ 35 years and smoker of ≥ 20 cigarettes/day; Use of metformin, thiazolidinediones, anti-hyperlipidemic drugs, anti-hypertensive drugs, glucocorticoids, or anti-androgens (spironolactone, flutamide, etc.) within 3 months; Documented or suspected illicit drug abuse or alcoholism within one year; Ingestion of any investigational drugs within 3 months prior to the study onset; and Pregnancy or lactation (≤ 6 weeks postpartum); Hematocrit < 33g/dL. These exclusion criteria are based on study requirements and also go beyond guidelines for OC use published by the World Health Organization.
Sites / Locations
- Virginia Commonwealth University General Clinical Research Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Obese women with metabolic syndrome
Obese women without metabolic syndrome
lean women without metabolic syndrome