Comparison between the success rate of standard method vs dose-dependent ovarian electrocautery in polycystic ovary syndrome
Not Applicable
Recruiting
- Conditions
- Infertility.Female infertility associated with anovulation
- Registration Number
- IRCT20171210037820N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Age: 18-38, Infertile women (duration more than 2 year)
with polycystic ovarian syndrome
cause of infertility: disorder of ovulation
Normal semen analysis in partner
Normal hystrosalpangography and laparoscopy
Interested for participation
Resistance to Clomiphene citrate
Exclusion Criteria
Other cause of infertility
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ovulation rate or pregnancy. Timepoint: every month up to 6 months. Method of measurement: Observing ovulation signs in serial transvaginal sonography or pregnancy.;Measuring progesterone level at 21th day of menstrual cycle. Timepoint: 21th day of first menstrual cycle after surgery. Method of measurement: According to level (ng/ml) / ELISA (Enzyme-linked immunosorbent assay) method.;LH, testosterone, and DHEAS serum level. Timepoint: Third day of first menstrual cycle after surgery. Method of measurement: According to LH (IU/ml) and testosterone (ng/dl) and DHEAS (µg/dl) level / ELISA (Enzyme-linked immunosorbent assay) method.
- Secondary Outcome Measures
Name Time Method