Polygenic Embryo Selection
Prospective Observational Outcome Comparison of Morphology- Versus Polygenic-Based Selection of In Vitro Fertilization-Derived Embryos
1 other identifier
observational
2,000
0 countries
N/A
Brief Summary
This study will evaluate whether IVF success rates after PRS-based embryo selection differ from those after morphology-based embryo selection, and whether polygenic disease risk correlates with embryo morphology.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2026
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 16, 2026
CompletedFirst Posted
Study publicly available on registry
September 25, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2029
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 30, 2029
September 25, 2026
September 1, 2026
3 years
September 16, 2026
September 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Sustained Implantation Rate
Ongoing pregnancy rate per embryo transfer at the time of discharge from IVF care
From enrollment to the end of treatment at 8-12 weeks
Secondary Outcomes (1)
Polygenic Score correlation with Embryo Morphology
Through study completion (3 years)
Study Arms (1)
IVF patients using preimplantation genetic testing
Eligibility Criteria
Cases (PRS): IVF patients/couples (intended parents) who elect to use PRS based embryo selection. Controls (Morphology): IVF patients/couples (intended parents) who elect to use morphology based embryo selection.
You may qualify if:
- Age 18 years or older
- Undergoing IVF and PGT at any clinic where Nucleus testing is used.
- Ability to provide informed consent and HIPAA authorization
You may not qualify if:
- Patients who decline research use of data
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 16, 2026
First Posted
September 25, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
September 30, 2029
Study Completion (Estimated)
September 30, 2029
Last Updated
September 25, 2026
Record last verified: 2026-09