Phase
Condition
Cardiovascular Disease
Chest Pain
Heart Attack (Myocardial Infarction)
Treatment
N/AClinical Study ID
Ages 21-40 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Normal menstrual cycles of 25-35 days in length for at least previous 3 cycles
21-40 years of age
BMI > 18, < 30
Serum P4 > 9 ng/ml on single sample collected between days 18-25 of self-reportedmenstrual cycle
Flexible schedule allowing morning blood draws on less than 48 hour notice
In good general health
Commit to remain on stable diet during study period (no changes to normal dietaryhabits)
Commit to using non-hormonal contraceptive methods during study period except thoseprescribed in the experimental protocol
No objections to taking study drugs
Exclusion
Exclusion Criteria:
Oral contraceptive use or other hormone supplement within the preceding 2 months
Long-acting hormonal contraceptive use in the past 12 months (e.g., Depo-Provera®)
Contraindications to study drugs
Current or past pregnancy within the previous 6 months or currently trying to conceive
Desiring to conceive in the next 8 months
Breastfeeding in the past 2 months
Diagnosed Diabetes or Metabolic Syndrome
Current or previous use of cholesterol lowering drugs within the preceding 12 months
Diagnosed Polycystic Ovary Syndrome
History of, or self-reported, substance abuse
Smoker
Previous infertility treatment excluding male factor issues
Use of an investigational drug within the past 2 months
Study Design
Study Description
Connect with a study center
Oregon Health & Sciences University, Department of Obstetrics and Gynecology, Women's Health Research Unit
Portland, Oregon 97239-3098
United StatesSite Not Available

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