Tracking outcomes after transferring embryos with non-euploid PGT-A results
The NEET Registry: a Prospective, Observational Study for Outcomes of Non-euploid Embryo Transfers (NEET)
Inception Fertility Research Institute, LLC · NCT07036536
This registry collects pregnancy and child health information from people using IVF who plan to transfer embryos with non-euploid PGT-A results to see what the outcomes are.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Sex | Female |
| Sponsor | Inception Fertility Research Institute, LLC (industry) |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT07036536 on ClinicalTrials.gov |
What this trial studies
The NEET Registry prospectively collects clinical, prenatal, neonatal, and pediatric outcome data from patients who undergo transfers of embryos with non-euploid PGT-A results (mosaic, isolated segmental, or whole-chromosome aneuploidy) within the Prelude Network. Participation requires informed consent and data are captured through participating fertility clinics and follow-up reports. No experimental interventions are given; the registry records real-world outcomes after frozen or fresh embryo transfer. Aggregated data will be analyzed to characterize pregnancy rates, pregnancy complications, birth outcomes, and early childhood health associated with different types of non-euploid results.
Who should consider this trial
Good fit: Ideal candidates are people planning to transfer an embryo with a non-euploid PGT-A result at a participating Prelude Network fertility clinic who can provide informed consent for registry follow-up.
Not a fit: People who are not transferring non-euploid embryos, who receive care outside the Prelude Network, or who do not consent to follow-up are unlikely to benefit directly from this registry's findings.
Why it matters
Potential benefit: If successful, this registry could provide clearer risk estimates for pregnancy and early child health after transferring mosaic or other non-euploid embryos, helping patients and clinicians make more informed decisions.
How similar studies have performed: Previous case series and small cohort reports have documented live births after mosaic embryo transfer, but long-term and broad outcomes data remain limited, so this registry expands on incomplete existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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. Exclusion Criteria: * Not applicable
Where this trial is running
Houston, Texas
- Inception Fertility Research Institute — Houston, Texas, United States (RECRUITING)
Study contacts
- Study coordinator: Amber Mendoza
- Email: amendoza@inceptionllc.com
- Phone: 346-393-2265
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Infertility, Mosaicism, Aneuploidy, IVF, PGT-A, aneuploid, FET