assess of effect of oral vitamin E on increase of intra uterine inseminization success in infertile me
Not Applicable
- Conditions
- Male infertility.Male infertility
- Registration Number
- IRCT2013122815961N1
- Lead Sponsor
- Shiraz University of Medical Sciences- Vice Chancellor for research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Inclusion criteria : Sperm count less than or equal to 15000000 CC ? progressive motility less than or equal to 32%? normal shaped sperm less than or equal to 4% according to WHO 2011 criteria for male infertility ? doing IUI for the first time
Exclusion criteria : not willing to cooperate in the project ? not willing to use vitamin E for any reason ? showing sensitivity to vitamin E
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sperm counts. Timepoint: After two mounts of treatment. Method of measurement: Semen analysis.;Sperm motility. Timepoint: After two mounts of treatment. Method of measurement: Semen analysis.;Percentage of normal shape sperm. Timepoint: After two mounts of treatment. Method of measurement: Semen analysis.
- Secondary Outcome Measures
Name Time Method Clinical pregnancy rate. Timepoint: 6-8 weeks after IVF. Method of measurement: By follow up of the patients and sonography.;Chemical pregnancy rate. Timepoint: 16-18 days after IVF. Method of measurement: By measurement of B-HCG.