Assessment of pregnancy rate by laparoscopic ovarian cautery in patients with poly cystic ovary syndrome and Previous failed IVF procedures
- Conditions
- infertility.Female infertility associated with anovulationN97.0
- Registration Number
- IRCT20090526001952N14
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 34
Women with poly cystic ovary syndrome who have two of the three diagnostic criteria Rotterdam at least
Age between 18- 35 year- old
Body mass index less than 30
Normal semen analysis in their spouse
Previous failed IVF procedures at least for 2 times
No laparoscopic contraindications
Aged more than 39 year
Previous ovarian surgery
Co-existing endocrine diseases including diabetes mellitus, estrogen-dependent tumors, thyroid disease, Cushing’s syndrome, or congenital adrenal hyperplasia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Chemical pregnancy rate. Timepoint: Beta-hCG test 14 days after embryo transfer. Method of measurement: Laboratory kits for Beta-hCG assay.;Clinical pregnancy rate. Timepoint: 6 to 7 weeks after embryo transfer. Method of measurement: Observing the gestational sac along with fetal heart activity in vaginal ultrasound.
- Secondary Outcome Measures
Name Time Method