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Automated Intracytoplasmic Sperm Injection (ICSIA)

Paired Non Inferiority Study Comparing Overture's Intracytoplasmic Sperm Injection Automated (ICSIA) System to the Standard Manual ICSI Process

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05633316
Acronym
ICSIA
Enrollment
10
Registered
2022-12-01
Start date
2022-12-05
Completion date
2024-11-30
Last updated
2023-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility, Female

Brief summary

The purpose of this research study is to evaluate Overture's automated Intracytoplasmic Sperm Injection (ICSIA) System. ICSIA is an investigational medical device that automates injection of sperm into eggs. This study will evaluate survival and fertilization rates of oocytes handled via ICSIA and compare to survival and fertilization rates of oocytes which are manually injected with sperm.

Detailed description

Today Intracytoplasmic Sperm Injection (ICSI) is performed manually; a highly skilled technician manually injects a single sperm cell into an oocyte using a set of microinjectors. Success of ICSI is contingent on operator skills and has a direct impact on the number of fertilized oocytes available and cumulative pregnancy rates. Automation of the ICSI technique may help improve consistency and efficiency of the process, as well as improve reproducibility across operators. Overture has developed the ICSI system to automate these critical processes, named ICSIA. ICSIA is composed of the same devices and consumables used for manual ICSI, but these devices have been integrated using a software interface with artificial intelligence to identify oocytes and allow for proper puncture of the oocyte and injection of the sperm without human intervention. The information from this study will be used by the study Sponsor, Overture Life, Inc, to help future development of the System and for submission of data to the United States Food and Drug Administration (FDA). During the study, patients will undergo a conventional IVF cycle, or donor IVF cycle. After the oocyte retrieval or thawing of donor oocytes, the oocytes will be placed into equal groups: test and control. Test group oocytes will undergo ICSI via ICSIA (the investigational device), and control group oocytes will undergo manual ICSI as is routinely performed. The oocytes will be immediately evaluated for survival and fertilization rates and remain separate for the duration of the study. ICSIA has been extensively tested in hamster and mice oocytes, and fertilization/survival rates after ICSIA have been between 89%-96%. After ICSI, conventional IVF processes will be followed and fertilized oocytes cultured up to blastocyst stage. Blastocysts will be biopsied for preimplantation genetic testing for aneuploidy (PGT-A) which assesses the embryo's chromosomes. All biopsied blastocysts will be frozen, and frozen embryo transfers (FET) scheduled after genetic results have been received. Embryo freezing and thaw will be performed manually. Selection of the embryo for transfer (whether test or control) will be at random.

Interventions

DEVICEInvestigational device named ICSIA

Oocytes will undergo intracytoplasmic sperm injection using the ICSIA (the investigational) device.

DEVICEManual ICSI

Oocytes will undergo intracytoplasmic sperm injection using the ICSI manual protocol

Sponsors

New Hope Fertility Center
CollaboratorOTHER
Overture Life
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

After the oocyte retrieval or thawing of donor oocytes, oocytes will be randomly assigned into equal groups: test and control. Test group oocytes will undergo ICSI via ICSIA (the investigational device), and control group oocytes will undergo manual ICSI as is routinely performed.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Infertile women undergoing IVF treatment with ICSI

Exclusion criteria

* Severe male factor infertility

Design outcomes

Primary

MeasureTime frameDescription
Survival ratesBetween 0 hours and 2 hours post-ICSIIt refers to the integrity of the oocytes after sperm injection out of the total number of oocytes injected.
Fertilization ratesBetween 16 hours and 20 hours post-ICSIIt refers to the number of oocytes that show to be correctly fertilized showing two pronuclei and a second polar body out of the total number of oocytes injected.

Secondary

MeasureTime frameDescription
Blastocyst ratesBetween 120 hours and 168 hours post-ICSIRefers to the number of fertilized embryos that develop into a good quality blastocyst after 5-7 days of in vitro culture
Euploidy rates1 month after biopsyRefers to the number of blastocysts that are biopsied that are diagnosed as euploid
Clinical pregnancy rates6 weeks after embryo transferRefers to the number of patients that are replaced with an embryo and result pregnant with fetal heartbeat out of the total patients that are transferred.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026