Assess of effect of oral vitamin E on increase of In Vitro Fertilization success in infertile me

Not Applicable

• Conditions: Male infertility.; Oligospermia NOS

• Registration Number: IRCT2014020616506N1
• Lead Sponsor: Shiraz University of Medical Sciences- Vice Chancellor for research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Inclusion conditions:
120 of the patients who have been candidated for IVF due to male infertility, have been diagnosed through the semen analysis upon WHO’s criteria and have satisfied the conditions of performing IVF based on existing criteria ( i.e. after semen processing, it contains less than 1-2 million motile sperms, or less than 10 million motile sperms in addition to more than 2 years infertility without any response to IUI ) will be studied.
Exclusion conditions:
If people are not willing to cooperate in the project or consuming vitamin E, for any reason and also show any sensitivity to vitamin E, will be excluded from the project.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparison of sperm counts. Timepoint: After two mounts of treatment. Method of measurement: Semen analysis.;Comparison of sperm motility. Timepoint: After two mounts of treatment. Method of measurement: Semen analysis.;Comparison of the percentage of normal shape sperm. Timepoint: After two mounts of treatment. Method of measurement: Semen analysis.

Secondary Outcome Measures

Name	Time	Method
Comparison of clinical pregnancy rate. Timepoint: 6-8 weeks after IVF. Method of measurement: By follow up of the patients and sonography.;Comparison of chemical pregnancy rate. Timepoint: 16-18 days after IVF. Method of measurement: By measurement of B-HCG.