Actively Recruiting
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
Eligibility Criteria
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.
You will not qualify if you...
- Not applicable
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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