Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Southern California
With
Society of Family Planning
Age
18–35
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
Women between ages 18-35 years
* Regular menstrual cycles (24-35 days) for the past 2 months
* Ovulatory at defined by midluteal progesterone level \>3 ng/mL (Day 18-25)
* Belongs to one of the following categories: normal weight (BMI = 18.5-24.9 kg/m2), obese (BMI = 30-39.9 kg/m2) or extremely obese (BMI ≥ 40 kg/m2)
* Participant has no intention of or desire to conceive (e.g., active attempt to become pregnant or in vitro fertilization) for the duration of the study
* Participant agrees to consistently use an effective method of nonhormonal contraception throughout the duration of study, which could include: condoms (male or female) with or without a spermicidal agent, diaphragm or cervical cap with spermicide, non-hormonal intra-uterine devise (IUD), or sterilization.
* Able to give informed consent
You may not be if
• Known renal or liver disease
* Known pituitary disorder
* Known adrenal disorder
* Known thyroid disorder
* Use of medication known to alter the cytochrome P450 system
* Use of depot-medroxyprogesterone acetate in the previous 6 months or any other hormonal contraceptive in the previous 3 months
