Skip to main content
Clinical Trials/NCT07464275
NCT07464275
Not yet recruiting
Not Applicable

A Retrospective, Observational, Multi-centered Study to Validate a D3-D5 Embryo Prediction Tool and Assess Its Performance in a Clinical Setting.

Future Fertility Inc.0 sites80 target enrollmentStarted: March 1, 2026Last updated:
InterventionsMAGENTA Blast

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Future Fertility Inc.
Enrollment
80
Primary Endpoint
The association between using MAGENTA Blast as an informative adjunctive aid and the prediction of blastocyst formation by Day 5 in embryos graded as Good/Fair

Overview

Brief Summary

This is a retrospective, observational, single-arm, multi-center study to evaluate the predictive performance of MAGENTA BLAST, an artificial intelligence (AI)-enabled software application, when used as analytical, adjunctive information to support Day 3 cleavage stage embryo predictions of blastocyst formation by Day 5.

Detailed Description

This retrospective, observational, single-arm, multi-centered study is designed to evaluate the predictive performance of MAGENTA Blast, an AI-enabled software, as adjunctive information to support Day 3 cleavage-stage embryo predictions of blastocyst formation by Day 5. The study will assess the association between embryo-level predictions generated using standard morphological evaluation with and without adjunctive MAGENTA Blast output, and observed blastocyst formation outcomes.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Women undergoing fresh IVF treatment using their own eggs
  • At least 18 years of age
  • Total antral follicle count (AFC) of at least 12 as measured by ultrasound prior to stimulation (in cases where AFC is performed)
  • Basal day 3 follicle-stimulating hormone levels (FSH) \< 10 IU (in cases where basal day 3 FSH is performed)
  • At least 8 normally fertilized eggs at the pronuclear (2PN) stage
  • Fertilization using only ejaculated sperm (fresh or frozen) - no surgically removed sperm
  • At least one two-cell embryo on Day 3
  • At least part of the embryo cohort is cultured until day 5 (i.e. 114-116 HPI)

Exclusion Criteria

  • Use of re-inseminated eggs (rescue ICSI)
  • Gestational carriers
  • Concurrent participation in another clinical study
  • Previous enrollment in this clinical study (i.e., one cycle data per patient)
  • History of cancer
  • Planned Day 3 laser-assisted hatching or embryos that underwent Day 3 biopsy for preimplantation genetic testing (PGT)
  • Low quality images
  • Lack of correlating reproductive outcomes (IVF lab results not available)

Arms & Interventions

Women undergoing fresh IVF treatment

Women undergoing fresh IVF treatment using their own eggs and are at least 18 years of age.

Intervention: MAGENTA Blast (Device)

Outcomes

Primary Outcomes

The association between using MAGENTA Blast as an informative adjunctive aid and the prediction of blastocyst formation by Day 5 in embryos graded as Good/Fair

Time Frame: 3 days

The association between blastocyst outcome predictions by Day 5 with adjunctive use of MAGENTA Blast and the observed blastocyst outcome (Yes/No) for embryos classified as Good/Fair quality will be quantified using Odds Ratio (OR) greater than 1 and corresponding 95% confidence intervals.

Secondary Outcomes

  • The association between using MAGENTA Blast as an informative adjunctive aid and the prediction of blastocyst formation by Day 5 in all embryos(3 days)
  • Blastocyst formation predicted by embryologists using traditional morphology only in all embryos as well as for the subset of embryos graded as Good/Fair(3 days)
  • The association per embryologist between adjunctive use of MAGENTA Blast for Day 3 cleavage-stage embryo assessment and prediction of blastocyst formation by Day 5 in embryos graded as Good/Fair(3 days)

Investigators

Sponsor
Future Fertility Inc.
Sponsor Class
Industry
Responsible Party
Sponsor

Similar Trials