Normal embryonic development relies on the correct transmission of genetic information, and sperm DNA plays a crucial part in this process. Causes of poor sperm DNA integrity include unhealthy lifestyles such as smoking and exposure to gonadotoxins, as well as, obesity, varicoceles, infections, advanced paternal age and systemic disorders. An increase in DNA fragmentation in sperm has been linked to lower fertilisation rate, poorer quality embryos, lower pregnancy rate, and high miscarriages rate. The best way for sperm selection and processing in assisted reproductive technologies (ART) should be noninvasive and cost-effective. It should also make it possible to identify high-quality spermatozoa and produce more favorable results in terms of pregnancy and live birth rates.7 Meanwhile, the microfluidic sperm separation technology is a less expensive and less invasive alternative. This method allows for the selection of motile sperm that have a normal morphology, low levels of reactive oxygen species (ROS), and low DFI
Study Type
OBSERVATIONAL
Enrollment
280
Clinique Ovo
Montreal, Quebec, Canada
Clinical Pregnancy Rate
Compare clinical pregnancy rate in couples with high Sperm DNA fragmentation
Time frame: approximately 8 weeks
Number of utilizable blastocysts obtained
Compare the number of utilizable embryos obtained in couples using TESA-ICSI vs Zymot-ICSI
Time frame: Approximately 20 days
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