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Automated Sperm Selection

Infertility

Intracytoplasmic sperm injection (ICSI) is one of the standard clinical treatments for infertility. ICSI involves the injection of a single sperm into an oocyte with a sharp micropipette. Injecting a sperm with DNA fragmentation (i.e., physical breakage of the DNA double strands) into the oocyte deterministically lowers the IVF fertilization rate \[1\]\[2\] and increases the miscarriage rate \[3\]\[4\]. Since the invention of ICSI in 1992, single sperm selection in ICSI has been made manually by embryologists, who select sperm by qualitatively choosing sperm with "good" motility and/or morphology based on their empirical experience. This involves significant subjectivity and inconsistency. We have developed a robotic system to select sperm with low sperm DNA fragmentation. Automated sperm selection also eliminates the subjectivity and inconsistency in manual sperm selection. The system consists of a camera to acquire images of sperm and a software to analyze the images. Embryologists select sperm by observing the same sperm characteristics as in the software criteria (e.g., speed etc.), but the software provides a more accurate and quantitative measure of sperm characteristics, thus ensuring the selected sperm have low DNA fragmentation.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    19 to 43

Participation Criteria

Inclusion Criteria:

* Patients undergoing ICSI
* Female partner between 19-43 years of age using own or donor oocytes

Exclusion Criteria:

* Patients who do not provide informed consent
* Patients with less than 6 mature eggs collected
* Patients undergoing IVF without ICSI
* Morphology \<4% normal forms
* 100% immotile sperm
* Cases where surgically-retrieved sperm is used for ICSI

Study Location

CReATe Fertility Centre
CReATe Fertility Centre
Toronto, Ontario
Canada

Contact Study Team

Backup Contact

Justin Tan

[email protected]
416-323-7727
Primary Contact

Clinical Research Coordinator

[email protected]
416-323-7727
Study Sponsored By
Create Fertility Center
Participants Required
More Information
Study ID: NCT05240469