Tracking outcomes after transferring embryos with non-euploid PGT-A results

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• Inception Fertility Research Institute
  Houston, Texas, United States Recruiting

Study contacts

• Study coordinator: Laurel Anderson
• Email: research@inceptionllc.com
• Phone: 3463621476

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.