About this trial
To determine how often embryos reported to be abnormal by preimplantation genetic testing result in liveborn infants. To evaluate whether the pregnancies that result from these embryos are higher risk for complications and whether the resulting babies have higher risk for health or developmental issues in the first five years after birth.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Available aneuploid or mosaic embryos
No other acceptable embryos available
Willing to travel to Stanford for treatment
English language fluency
Disqualifiers
Use of international donor eggs or sperm not tested according to FDA guidelines.
Living outside the United States
Embryos with Triploidy are not eligible for transfer in this protocol
Trial design
Parallel
Treatments tested in this trial
Non-euploid embryo transfer
Other interventionOther than choice of embryo for transfer, all other medical interventions will be standard of care protocols
Euploid Transfer
Other interventionStandard of Care Protocol
Treatment groups
Trial outcomes
Primary outcomes
Pregnancy Rate
Number participants who undergo embryo transfers that lead to a positive pregnancy test
Secondary outcomes
Live birth rate
Number participants who conceive after embryo transfer and have a live birth.
Obstetric complications
Number of participants who have a maternal of fetal complication after embryo transfer
Pediatric Development
Number of newborns and children who have abnormal pediatric development at 3 months, 2 years and 5 years following birth
Sponsors and contacts
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