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Assessment of pregnancy rate by laparoscopic ovarian cautery in patients with poly cystic ovary syndrome and Previous failed IVF procedures

Not Applicable
Conditions
infertility.
Female infertility associated with anovulation
N97.0
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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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