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Digital twin could revolutionize IVF success predictions

NCT ID NCT07305480

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This observational study aims to create a digital twin model that predicts whether an embryo will implant successfully during IVF. Researchers will analyze de-identified data from one participant, including clinical, molecular, and biochemical information. The model does not affect treatment decisions and is only used for research. If it works, it may help doctors choose the best embryos for transfer.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to a tool that helps doctors predict which embryos are most likely to implant, potentially improving IVF success rates.
What could go wrong
This is a very early, small study with only one participant, so results may not apply broadly. The model is not yet proven and may not improve real-world outcomes.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

1 person

The number who actually took part.

Started

Jan 2023

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population includes women undergoing in vitro fertilization (IVF) treatment whose embryo-related clinical, laboratory, molecular, and biochemical data are collected as part of routine clinical care. The dataset consists of fully de-identified non-image embryo development information, including text-based morphological descriptions, PGT-A results, secretome and exosomal biomarkers, endometrial receptivity profiles, and IVF cycle parameters required to construct and validate a multimodal digital twin model of blastocyst implantation potential. Participants represent typical reproductive-age IVF patients receiving standard ovarian stimulation, oocyte retrieval, embryo culture, assessment, and embryo transfer procedures. No experimental interventions, investigational drugs, or investigational devices are used. Only retrospective and/or prospectively collected routine clinical data are analyzed for computational model development.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Women undergoing in vitro fertilization (IVF) treatment at participating fertility clinics. * Availability of non-image embryo development data. * Availability of text-based morphological embryo descriptions. * Availability of PGT-A results. * Availability of secretome and exosomal biomarker data. * Availability of molecular and biochemical data collected during routine clinical care. * Availability of IVF cycle parameters collected during routine clinical workflow. * Embryos evaluated according to standard clinic protocols with documented implantation outcomes. * Age of the oocyte provider between 20 and 42 years. * Signed informed consent allowing use of fully de-identified clinical, laboratory, molecular, and follow-up data. Exclusion Criteria: * Embryos lacking sufficient non-image developmental data required for digital twin generation or implantation outcome assessment. * Use of donor oocytes or donor embryos when linkage with required clinical or laboratory metadata is not possible. * Cases in which implantation outcome cannot be confirmed. * Presence of severe uterine abnormalities prior to embryo transfer that may affect implantation reliability. * Withdrawal of consent for use of anonymized clinical, laboratory, or follow-up data.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Ukrainian Association of Biobanks Austria - Digital Twin Lab

    Graz, 8010, Austria

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