Evaluation of SiD's System for Improving Assisted Reproduction Treatments

NCT05611164 | Completed

• 1 other identifier: P002-SP002
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 2

Brief Summary

According to the WHO, infertility affects 15% of reproductive age couples worldwide. Among the assisted reproductive technologies available for patients with infertility, intracytoplasmic sperm injection (ICSI) has become one of the most widely employed and is now thought to be the most common method for oocyte insemination outside of the human body. ICSI entails the selection of an individual sperm cell and its injection directly into an oocyte. Usually, an embryologist performs the selection of the individual sperm cell to inject by subjectively observing the morphology and progression of the candidate spermatozoon. Subjectivity and time constrains, however, suggest the best possible candidate might not always be selected. Further optimization of ICSI technology remains a significant goal, yet the majority of approaches proposed in the literature have returned mixed results. The deployment of an artificial intelligence (AI) software capable of detecting and non-invasively predicting the value of individual spermatozoa in real time could significantly improve ICSI. SiD (IVF 2.0 Ltd, London, UK) is a software designed to identify, evaluate, and assist in the spermatozoon selection process ahead of ICSI. SID uses a mathematical model to evaluate individual spermatozoa in real-time according to their motility patterns (for instance velocity, linearity, straightness) and their morphology. The software has been developed by making use of retrospective data analysis, but its prospective evaluation is still pending. With the above in mind, this study intends to address the following question: can the use of a software assistant for the selection of individual sperm cells for injection (SiD), improve ICSI outcomes (oocyte fertilization, embryo development and quality, embryo ploidy, pregnancy, and live birth)? Patients with a clinical indication for undergoing ICSI will be prospectively enrolled into the study. Following ovarian stimulation, the oocytes retrieved from each patient will be randomly split into two groups and inseminated by ICSI using sperm selected either subjectively by an embryologist (control group) or by the software assistant SiD (experimental group). Embryos will be allowed to develop for up to six days and until blastocyst formation assessments are completed. Embryos might be subjected to cytogenetic screening or used for embryo transfer according to patient needs. The recorded outcomes will be anonymized prior to statistical analysis.

Conditions

Infertility

Outcome Measures

Primary Outcomes (3)

• Fertilization rate

  Rate of oocytes that present two pronuclei or cell division

  16-18 hours after ICSI

• Blastocyst formation rate

  Rate of oocytes that have a defined trophectoderm and inner cell mass

  around 120 hours after ICSI

• Usable blastocyst formation rate

  Rate of oocytes that have a blastocyst that is transferable accoring to its quality

  around 120 hours after ICSI

Secondary Outcomes (3)

• Ploidy status

  trophectoderm biopsy is performed around 120 hours after ICSI

• Biochemical pregnancy

  2 weeks after blastocyst transference

• Clinical pregnancy

  6 weeks after blastocyst transference

Study Arms (2)

Sperm selected by embryologist without software assistance

NO INTERVENTION

For each patient, oocytes collected following one ovarian stimulation cycle are randomly distributed in two groups ("no intervention" and "experimental" arms), in a sibling oocyte study design. In the "no intervention" arm, the individual spermatozoa for injection are selected subjectively by the embryologist.

Sperm selected with AI assistant SiD

EXPERIMENTAL

For each patient, oocytes collected following one ovarian stimulation cycle are randomly distributed in two groups ("no intervention" and "experimental" arms), in a sibling oocyte study design. In the "experimental" arm, the spermatozoa selection for injection is performed based on the recommendation of the AI assistant SiD.

Device: Software assisted selection of individual spermatozoa for intracytoplasmic sperm injection

Interventions

Software assisted selection of individual spermatozoa for intracytoplasmic sperm injection DEVICE

Half of the oocytes will be injected with a sperm selected with SiD's assistance

Sperm selected with AI assistant SiD

Eligibility Criteria

• Age: 18 Years - 40 Years
• Sex: female
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Participant's age between 18 and 40 years of age.
• Informed consent signed by the patient before treatment.
• IVF treatments with medical or embryology indication to perform ICSI.
• Cycles with at least 2 oocytes in Metaphase II.
• Fresh ejaculated motile sperm.
• Fresh oocytes.
• Selection of sperm using a 7% or 10% PVP solution.
• Presence of motile sperm at the time of sperm selection for ICSI.
• Videos recorded with a total magnification of 200x.

You may not qualify if:

• Patients diagnosed with recurrent pregnancy loss.
• Spermatozoa extracted by testicular biopsy.
• Frozen/thawed spermatozoa.
• Frozen/thawed oocytes in any case.
• That the recommendations for use of SiD have not been fully followed.
• Poor quality of saved ICSI video.
• Inability to reliably trace sperm-oocyte-embryo throughout the process.
• Oocytes that are not in Metaphase II.
• Patients with immotile sperm

Sponsors & Collaborators

• IVF 2.0 Limited: lead
• New Hope Fertility Center Mexico: collaborator

Study Sites (2)

New Hope Fertility Center

Guadalajara, Jalisco, 44630, Mexico

Location

New Hope Fertility Center

Mexico City, 11000, Mexico

Location

MeSH Terms

Conditions

Infertility

Interventions

Sperm Injections, Intracytoplasmic

Condition Hierarchy (Ancestors)

Genital Diseases; Urogenital Diseases

Intervention Hierarchy (Ancestors)

Fertilization in Vitro; Reproductive Techniques, Assisted; Reproductive Techniques; Therapeutics; Investigative Techniques

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 3, 2022
• First Posted: November 9, 2022
• Study Start: April 1, 2022
• Primary Completion: September 5, 2022
• Study Completion: October 31, 2022
• Last Updated: November 14, 2022

Record last verified: 2022-11

Data Sharing

• IPD Sharing: Will not share

Locations

ME (2)