Endometrial Receptivity Prediction During in Vitro Fertilization Using Artificial Intelligence
NCT ID: NCT06717802
Last Updated: 2025-09-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
1500 participants
OBSERVATIONAL
2025-06-01
2028-12-31
Brief Summary
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Participation in the study is voluntary, involves no additional testing or intervention beyond routine procedures, and consent can be withdrawn verbally or in writing at any time without cause or adverse consequences.
Over a three-year period, the trial is expected to enrol approximately 1,500 patients between the ages of 18 and 40 who are indicated for IVF treatment and who volunteer for treatment.
Patients enrolled in the study will not be required to attend more clinic visits during treatment than they would otherwise have to. During the trial, certain patient-specific data (age, indication for treatment, body mass index), stimulation-specific data (duration of stimulation, type and dose of drug, endometrial thickness), ultrasound scans and outcome-specific data (treatment failure, biochemical pregnancy, clinical pregnancy) will be collected. The data will be stored in a secure database. The data collected during the study will only be accessible to the professionals involved in the study and no information, including personal data, will be disclosed to third parties.
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Detailed Description
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As the quality of imaging has improved, the focus has shifted to analyzing the pattern of the endometrium, the latest research using artificial intelligence.
The aim of this study is to investigate whether segmentation and analysis of the endometrium using artificial intelligence in vaginal ultrasound images taken during stimulation and on the day of transfer can help to more accurately determine the receptivity of the endometrium. The significance of this is that in case of poor implantation chances it is possible to freeze the embryo(s) and have the opportunity to implant the embryo in a subsequent natural or hormone replacement therapy cycle, possibly with better chances.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Maximum 3 unsuccessful previous embryo transfers
* Only cycles in which single blastocyst is transferred
Exclusion Criteria
* Presence of hydrosalpinx
* Endometriosis
* Planned freeze-all cycle
* Positive hepatitis B, hepatitis C or HIV screening test
18 Years
40 Years
FEMALE
No
Sponsors
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Dunamenti REK Reprodukcios Kozpont
UNKNOWN
Gottsegen National Cardiovascular Institute
OTHER
Responsible Party
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Márton Kolossváry
Head of Education and Research
Locations
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Dunamenti REK Reprodukcios Kozpont
Budapest, , Hungary
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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endoAI
Identifier Type: -
Identifier Source: org_study_id
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