Comparison of clinical outcomes in tow sperm selection procedure
Not Applicable
- Conditions
- Male factor infertility.Male infertility
- Registration Number
- IRCT201504307223N3
- Lead Sponsor
- Royan Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Primary male factor infertility (at least, two of their semen parameters were considered as abnormal according to the WHO-2010)
Exclusion criteria: Females factor infertility basely WHO criteria (2010) with higher than 35 years and less than 6 oocytes
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sperm motility. Timepoint: In daye of ICSI procedure. Method of measurement: Using optical microscope, based WHO criteria.;Sperm concentration. Timepoint: In daye of ICSI procedure. Method of measurement: Using optical microscope, based WHO criteria.;Sperm morphology. Timepoint: In daye of ICSI procedure. Method of measurement: Using optical microscope, based WHO criteria.;Fertilization rate. Timepoint: 24 hours after ICSI procedure. Method of measurement: View of 2 pronucleuse with invert microscp.;Chemical pregnancy. Timepoint: 18 days after ICSI procedure. Method of measurement: Measurement of Beta HCG level in serum.;Quality of embryo. Timepoint: Three days post-oocyte retrieval. Method of measurement: Using a three-point scoring system including fragmentation rate, number of blastomere, shape and size.;Clinical l pregnancy. Timepoint: 12 weeks after ICSI procedure. Method of measurement: Fetal heart beat.
- Secondary Outcome Measures
Name Time Method