Comparison of dualL-Trigger and hcg-Trigger on infertile patients with normal ovarian response
Not Applicable
- Conditions
- infertility.N97.0,N97.Female infertility associated with anovulation,Female infertility of tubal origin,Female infertility associated with male factors,Female infertility of other origin,Female infertility, unspecified,
- Registration Number
- IRCT2015061722795N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 126
Inclusion Criteria
inclusion criteria:
age18-40 years;regular mense(25-34 days);BMI between 18-35;FSH days 3 <10
exclusion criteria:
FSH days 3 >=10;AMH=<1.1;expectancy for ovarian hyper response(>=16 follicles on the last trans vaginal sonography );endocrine deases(DM ,hyperprolactinemia,thyroide dysfunction ,CAH,cushing syndrome);PCOs;uterine anomaly in HSG or hysteroscopy;sever male factor(azospermia require to TESE or PESA);history of OHSS;criteria of ovarian hyper response or ovarian poor response
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of Metaphase II oocyte. Timepoint: on oocyte retrieval day. Method of measurement: evaluation by embryologist under microscope.;Number of Metaphase II oocytse ,total number of oocytes,number of embryoss. Timepoint: oocyte retrieval day,day3 after oocyte retrieval or IVF. Method of measurement: evaluation under microscope by an embryologist and scoring by scientific evidence.
- Secondary Outcome Measures
Name Time Method Biochemical pregnancy ,clinical pregnancy,abortion ,OHSS. Timepoint: two weeks after transfer for biochemical pregnancy,4weeks for clinical pregnancy,2 weeks after transfer for OHSS. Method of measurement: BHCG for biochemical ,trans vaginal sonography for clinical,clinical evaluation for OHSS.