Selecting optimized method for ovulation inductio
Phase 3
- Conditions
- infertility.Female infertility
- Registration Number
- IRCT201106236871N1
- Lead Sponsor
- Vice chancellor for research, Bushehr University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 104
Inclusion Criteria
Infertile anovulating PCO women in reproductive age of 18-30 and BMI of 19-25. Exclusion criteria: Any abnormality in thyroid and prolactin tests; structural abnormalities of uterus and tubes; metabolic disorders; cardiac and liver disease; cushing disease and OCP users.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pregnancy. Timepoint: 14 days after ovulation. Method of measurement: ßhCG Test.;Adequate follicle (16-22mm). Timepoint: 13th - 14th day of mensturation cycle. Method of measurement: Vaginal sonography.;Serum progestron level. Timepoint: The 21th day of mensturation cycle. Method of measurement: Biochemical methods for measuring progestron titer.;Alive fetus. Timepoint: The 7th week of pregnancy. Method of measurement: Vaginal sonography.
- Secondary Outcome Measures
Name Time Method Multiple pregnancy. Timepoint: 7th week. Method of measurement: Ultasonography.