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Automated Intracytoplasmic Sperm Injection (ICSIA) (ICSIA)

Primary Purpose

Infertility, Female

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Investigational device named ICSIA
Manual ICSI
Sponsored by
Overture Life
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Infertility, Female

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Infertile women undergoing IVF treatment with ICSI Exclusion Criteria: Severe male factor infertility

Sites / Locations

  • New Hope Fertility Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

ICSIA

Control

Arm Description

Intracytoplasmic sperm injection will be performed using the automated system named ICSIA (investigational device)

In this control group oocytes will undergo manual ICSI as is routinely performed.

Outcomes

Primary Outcome Measures

Survival rates
It refers to the integrity of the oocytes after sperm injection out of the total number of oocytes injected.
Fertilization rates
It 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 Outcome Measures

Blastocyst rates
Refers to the number of fertilized embryos that develop into a good quality blastocyst after 5-7 days of in vitro culture
Euploidy rates
Refers to the number of blastocysts that are biopsied that are diagnosed as euploid
Clinical pregnancy rates
Refers 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.

Full Information

First Posted
October 31, 2022
Last Updated
July 5, 2023
Sponsor
Overture Life
Collaborators
New Hope Fertility Center
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1. Study Identification

Unique Protocol Identification Number
NCT05633316
Brief Title
Automated Intracytoplasmic Sperm Injection (ICSIA)
Acronym
ICSIA
Official Title
Paired Non Inferiority Study Comparing Overture's Intracytoplasmic Sperm Injection Automated (ICSIA) System to the Standard Manual ICSI Process
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 5, 2022 (Actual)
Primary Completion Date
November 30, 2023 (Anticipated)
Study Completion Date
November 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Overture Life
Collaborators
New Hope Fertility Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Female

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ICSIA
Arm Type
Experimental
Arm Description
Intracytoplasmic sperm injection will be performed using the automated system named ICSIA (investigational device)
Arm Title
Control
Arm Type
Experimental
Arm Description
In this control group oocytes will undergo manual ICSI as is routinely performed.
Intervention Type
Device
Intervention Name(s)
Investigational device named ICSIA
Intervention Description
Oocytes will undergo intracytoplasmic sperm injection using the ICSIA (the investigational) device.
Intervention Type
Device
Intervention Name(s)
Manual ICSI
Intervention Description
Oocytes will undergo intracytoplasmic sperm injection using the ICSI manual protocol
Primary Outcome Measure Information:
Title
Survival rates
Description
It refers to the integrity of the oocytes after sperm injection out of the total number of oocytes injected.
Time Frame
Between 0 hours and 2 hours post-ICSI
Title
Fertilization rates
Description
It 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.
Time Frame
Between 16 hours and 20 hours post-ICSI
Secondary Outcome Measure Information:
Title
Blastocyst rates
Description
Refers to the number of fertilized embryos that develop into a good quality blastocyst after 5-7 days of in vitro culture
Time Frame
Between 120 hours and 168 hours post-ICSI
Title
Euploidy rates
Description
Refers to the number of blastocysts that are biopsied that are diagnosed as euploid
Time Frame
1 month after biopsy
Title
Clinical pregnancy rates
Description
Refers 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.
Time Frame
6 weeks after embryo transfer

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Infertile women undergoing IVF treatment
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infertile women undergoing IVF treatment with ICSI Exclusion Criteria: Severe male factor infertility
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Zhang, MD
Organizational Affiliation
New Hope Fertility Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
New Hope Fertility Center
City
New York
State/Province
New York
ZIP/Postal Code
10019
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Automated Intracytoplasmic Sperm Injection (ICSIA)

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