Comparing the efficacy of long-term and short-term doses of letrozole in ovulation induction among patients with polycystic ovary syndrome
Not Applicable
- Conditions
- polycystic ovary syndrome.E28.2
- Registration Number
- IRCT2016030926962N2
- Lead Sponsor
- Vice chancellor for research Urmia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
Age 38-18 years - poly cystic ovary syndrome proven - resistance to clomiphene citrate thyroid -Tested normal - normal prolactin - the absence of other causes of infertility, including male factor - normal Hysterosalpangiography
Exclusion criteria: Ovarian Cysts- Follicle-stimulating hormone> 10 - Patients with Ovarian Hyper stimulation Syndrome
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The number of mature follicles. Timepoint: 11 cycle days after intervention. Method of measurement: Vaginal ultrasound.;Endometrial thickness at the time of HCG injection. Timepoint: 11 cycle days after intervention. Method of measurement: Vaginal ultrasound.;The number of Gonal. Timepoint: After intervantion, days 5, 7 and 9 of the cycle. Method of measurement: Vaginal ultrasound.
- Secondary Outcome Measures
Name Time Method Event Pregnancy. Timepoint: After intervention. Method of measurement: Test BHCG.;Abortion rate. Timepoint: After intervention. Method of measurement: Clinical and sonographic reports.;Multiple event. Timepoint: After intervention. Method of measurement: Ultrasound Report.