Actively Recruiting

FEMALE
ID07036536

The NEET Registry: a Prospective, Observational Study for Outcomes of Non-euploid Embryo Transfers (NEET)

Led by Inception Fertility Research Institute, LLC · Updated on 2025-06-25

1000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

I

Inception Fertility Research Institute, LLC

Lead Sponsor

C

CooperSurgical Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to gather information about the outcomes of non-euploid embryo transfers (NEET) in patients undergoing in vitro fertilization (IVF) within The Prelude Network. It focuses on embryos with chromosomal abnormalities such as mosaicism, isolated segmental aneuploidy, or whole chromosome aneuploidy, which are sometimes transferred for specific patient reasons. The study seeks to better understand prenatal, neonatal, and pediatric results for these types of embryo transfers to help inform future decisions. The study is observational, tracking patients who plan to transfer non-euploid embryos. Data collection includes prenatal through pediatric stages to observe the effects of these transfers over time. There are no interventions or treatment groups since it records outcomes of standard clinical decisions about embryo transfer. Participants will be monitored through follow-up assessments that capture implantation rates over five years, along with other health outcomes in early life. Researchers will collect detailed information from fertility clinics to evaluate the success and safety of non-euploid embryo transfers. The study's duration and data collection allow for long-term understanding of these transfers' effects.

CONDITIONS

Brief Title

Non-Euploid Embryo Transfer (NEET) Registry

Who Can Participate

FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient is planning a non-euploid embryo transfer (NEET) at a fertility clinic in The Prelude Network.
  • Patient has signed informed consent to participate in the registry.
Not Eligible

You will not qualify if you...

  • Not applicable

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Up to 5 years

Participants who undergo non-euploid embryo transfer are observed to collect prenatal, neonatal, and pediatric outcome information.

Trial Site Locations

Total: 1 location

1

Inception Fertility Research Institute

Houston, Texas, United States, 77081

Actively Recruiting

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Research Team

A

Amber Mendoza

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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