Overview
Endocrinology Profile in Patients Undergoing Clomiphene, Letrozole, and Combination Clomiphene and Letrozole Cycles
Status:
Unknown status
Unknown status
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The goal of the study is to measure serial hormonal levels in patients undergoing clomiphene, letrozole, and a combination clomiphene and letrozole cycle. This information may help us to optimize less expensive medications for ovulation induction, reduce the number of treatment cycles to achieve a successful pregnancy, and use a medication regimen that may result in fewer multiple gestation pregnancies.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
University Hospitals Cleveland Medical CenterTreatments:
Clomiphene
Enclomiphene
Letrozole
Zuclomiphene
Criteria
Inclusion Criteria:- Age 18-40 years old
- Body mass index (BMI) > 18 kg/m^2 and < 40kg/m^2
- No contraindications to clomiphene or letrozole
- Ovulatory women
- 1 month without any fertility medication
Exclusion Criteria:
- Patients unable to consent for the study
- Patients with polycystic ovarian syndrome or anovulatory women