Non-Euploid Embryo Transfer (NEET) Registry
The NEET Registry: a Prospective, Observational Study for Outcomes of Non-euploid Embryo Transfers (NEET)
1 other identifier
observational
1,000
1 country
1
Brief Summary
The NEET Registry is a registry to track and study the outcomes of non-euploid embryo transfers (NEET) in The Prelude Network
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2024
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 23, 2024
CompletedFirst Submitted
Initial submission to the registry
October 2, 2024
CompletedFirst Posted
Study publicly available on registry
June 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2030
June 25, 2025
June 1, 2025
6.2 years
October 2, 2024
June 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Rate of Embryo Implantation
The frequency of positive pregnancy test (blood serum QHCG) 10-14 days post embryo transfer
5 years
Other Outcomes (4)
Rate of Ongoing Pregnancy
5 years
Rate of Live Birth
5 years
Rate of Spontaneous Abortion
5 years
- +1 more other outcomes
Eligibility Criteria
Patients planning a non-euploid embryo transfer (NEET) at a fertility clinic in The Prelude Network.
You may qualify if:
- 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 may not qualify if:
- Not applicable
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Inception Fertility Research Institute, LLClead
- CooperSurgical Inc.collaborator
- Igenomixcollaborator
Study Sites (1)
Inception Fertility Research Institute
Houston, Texas, 77081, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 5 Years
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 2, 2024
First Posted
June 25, 2025
Study Start
September 23, 2024
Primary Completion (Estimated)
December 1, 2030
Study Completion (Estimated)
December 1, 2030
Last Updated
June 25, 2025
Record last verified: 2025-06