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Automation of Gamete Preparation, Intracytoplasmic Sperm Injection (ICSI), Embryo Culture, and Vitrification

Primary Purpose

Infertility

Status
Not yet recruiting
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Gamete preparation, ICSI, embryo culture and vitrification robot assistant
Routine Manual ICSI Workflow
Sponsored by
Conceivable Life Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Infertility

Eligibility Criteria

undefined - 50 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Medical indication to perform ICSI. Informed consent signed by the patients before treatment. Medical indication for the use of autologous or donor oocytes. Medical indication for the use of autologous or donor sperm. Motile sperm. Exclusion Criteria: Recurrent pregnancy loss. Previous history of total fertilization failure. Surgical sperm retrieval. Severe male factor infertility. Known semen liquefaction problems. Any other case abnormalities that could potentially reduce success rates according to the criteria of the senior embryologist in charge.

Sites / Locations

  • New Hope Fertility Centre, Guadalajara
  • New Hope Fertility Centre, Mexico City

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Test group (Robot-assisted gamete preparation, ICSI, embryo culture and vitrification)

Control group (routine manual ICSI workflow)

Arm Description

Outcomes

Primary Outcome Measures

Timing
Time to complete each automated procedure
Efficiency
proportion of automated procedures achieving their goal
Autonomy
proportion of completed procedure not requiring human intervention
Walk-away time
time savings realized by an embryologist who is able to attend other duties while the robotic assistant is at work

Secondary Outcome Measures

Sperm survival and quality (seminogram)
Proportion of oocytes fertilized
Embryos survival and quality (by morphology assessment)
Clinical pregnancy rates following embryo transfer

Full Information

First Posted
October 4, 2023
Last Updated
October 4, 2023
Sponsor
Conceivable Life Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT06074835
Brief Title
Automation of Gamete Preparation, Intracytoplasmic Sperm Injection (ICSI), Embryo Culture, and Vitrification
Official Title
Automation of Gamete Preparation, Intracytoplasmic Sperm Injection (ICSI), Embryo Culture, and Vitrification: A Proof of Concept Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 30, 2023 (Anticipated)
Primary Completion Date
October 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Conceivable Life Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Patients suffering from infertility may seek assisted conception treatment. In a full treatment cycle, the sperm and eggs (gametes) from the intended parents will be looked after by skilled laboratory staff (embryologists) who will rely on manual laboratory processes to achieve fertilization. The most commonly employed method to achieve fertilization is intracytoplasmic sperm injection (ICSI), a treatment that involves the injection of a single sperm cell directly inside an egg. The embryos so obtained are then be maintained in an appropriate environment (incubator) for several days before deciding whether they can be immediately used to attempt to establish a pregnancy (embryo transfer), or should be frozen in preparation for a future treatment (cryopreservation). The laboratory steps required to complete a full assisted conception treatment (from sperm and egg retrieval, to fertilization, and then to embryo transfer and/or cryopreservation) are often manual and time-consuming, and thus the success of the treatment is highly dependent on the skill of individual staff and outcomes can be affected by fatigue, stress, and workload. The combination of robotics and artificial intelligence (AI) has the potential to provide improvements to, and standardize, the fertility laboratory, but such integration has not been achieved routinely. Other medical fields, such as regenerative medicine, have long benefited from the implementation of robotic solutions; however, modern automation has yet to find its way into the fertility laboratory. The goal for Conceivable Life Sciences (the study sponsor) is the delivery of a suite of solutions that, collectively, will allow a fully autonomous ICSI cycle to take place (from sperm/egg preparation, to sperm injection, to embryo culture and cryopreservation) in an effort to reduce costs, assist laboratory staff, and possibly, improve outcomes. The purpose of this study is to deliver a core aspect of this project: the digital control and individual automation of all key steps of a complete laboratory workflow. The data generated in this study will help the future development of these automated systems. Patients undergoing an ICSI treatment may be recruited in this study. Their gametes (sperm and/or eggs) may be distributed across two groups (test and control) and undergo one or more elements of an automated full assisted conception workflow (for the test group) or a standard assisted conception workflow (for the control group). Robotic automation may include any of the following steps: robotic sperm preparation, robotic oocyte selection and denudation, robotic sperm injection, automated embryo culture, and automated cryopreservation. The resulting embryos may be employed for embryo transfer. The main hypothesis of this study is that the use of robotic assistants as part of a full assisted conception cycle may improve laboratory workflows without reducing the treatment success rates.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Test group (Robot-assisted gamete preparation, ICSI, embryo culture and vitrification)
Arm Type
Experimental
Arm Title
Control group (routine manual ICSI workflow)
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
Gamete preparation, ICSI, embryo culture and vitrification robot assistant
Intervention Description
Patients undergoing an assisted conception treatment with medical indication to perform ICSI may be recruited in this study. The study will follow a sibling-oocyte and/or sibling embryo study design where oocytes and/or embryos obtained from a specific patient or couple will be randomly distributed across two groups (test and control) and undergo one or more elements of an automated assisted conception laboratory workflow (for the test group) or a standard assisted conception laboratory workflow (for the control group). Before distributing the samples, an embryologist will slightly blur the vision of the samples so that their morphology can no longer be clearly assessed. Robotic automation may include any of the following steps: robotic sperm preparation, robotic oocyte selection and denudation, robotic sperm injection, automated embryo culture, and automated cryopreservation. The resulting embryos may be employed for embryo transfer.
Intervention Type
Other
Intervention Name(s)
Routine Manual ICSI Workflow
Intervention Description
Routine Manual Icsi Workflow
Primary Outcome Measure Information:
Title
Timing
Description
Time to complete each automated procedure
Time Frame
6 weeks from enrolment
Title
Efficiency
Description
proportion of automated procedures achieving their goal
Time Frame
6 weeks from enrolment
Title
Autonomy
Description
proportion of completed procedure not requiring human intervention
Time Frame
6 weeks from enrolment
Title
Walk-away time
Description
time savings realized by an embryologist who is able to attend other duties while the robotic assistant is at work
Time Frame
6 weeks from enrolment
Secondary Outcome Measure Information:
Title
Sperm survival and quality (seminogram)
Time Frame
6 weeks from enrolment
Title
Proportion of oocytes fertilized
Time Frame
6 weeks from enrolment
Title
Embryos survival and quality (by morphology assessment)
Time Frame
6 weeks from enrolment
Title
Clinical pregnancy rates following embryo transfer
Time Frame
8 weeks from enrolment

10. Eligibility

Sex
All
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Medical indication to perform ICSI. Informed consent signed by the patients before treatment. Medical indication for the use of autologous or donor oocytes. Medical indication for the use of autologous or donor sperm. Motile sperm. Exclusion Criteria: Recurrent pregnancy loss. Previous history of total fertilization failure. Surgical sperm retrieval. Severe male factor infertility. Known semen liquefaction problems. Any other case abnormalities that could potentially reduce success rates according to the criteria of the senior embryologist in charge.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amaranta Martinez, MD
Phone
+52 800 8905884
Email
dra.amaranta@nhfc.mx
Facility Information:
Facility Name
New Hope Fertility Centre, Guadalajara
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44630
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amaranta Martinez, MD
First Name & Middle Initial & Last Name & Degree
Alejandro Chavez-Badiola, MD
Facility Name
New Hope Fertility Centre, Mexico City
City
Mexico City
ZIP/Postal Code
11000
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amaranta Martinez, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data sharing is subject to ethical, legal, and privacy considerations. We are committed to following established guidelines and best practices for data sharing. IPD that underlie results in a publication will be shared as part of either the publication itself or its underlying supporting figures/tables.
IPD Sharing Time Frame
within 2y of study completion

Learn more about this trial

Automation of Gamete Preparation, Intracytoplasmic Sperm Injection (ICSI), Embryo Culture, and Vitrification

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