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Machine-Learning Prediction of Pregnancy Outcomes After Assisted Reproductive Treatments

3 ottobre 2026 aggiornato da: BetaPlus Center for Reproductive Medicine

Development and Validation of a Machine Learning Prognostic Model for Early Prediction of Pregnancy Outcomes Following Assisted Reproductive Treatment: A Retrospective and Prospective Cohort Study

The goal of this observational study is to develop and validate a machine-learning model to predict pregnancy outcomes in women with a positive pregnancy test following assisted reproductive treatment (ART), with the primary analysis focusing on in vitro fertilization (IVF) and frozen embryo transfer (FET). The study will also include an exploratory analysis of pregnancies following intrauterine insemination (IUI). The main questions addressed by the study are:

Can early blood levels of beta-human chorionic gonadotropin (beta-hCG) predict the likelihood of live birth in an IVF or FET cycle? Can early beta-hCG levels help identify pregnancies at increased risk of biochemical pregnancy or early pregnancy loss?

Participants will have clinical and treatment information, including beta-hCG measurements and pregnancy outcomes, collected from medical records or during prospective follow-up. No changes to participants' medical treatment will be made as part of the study.

Panoramica dello studio

Descrizione dettagliata

Infertility affects more than 15% of the global population, and ART are increasingly used to achieve pregnancy. The field continues to evolve rapidly with ongoing technological and clinical advances. Although these advances have improved ART, success rates continue to vary, contributing to significant psychological distress among patients due to uncertainty regarding outcomes.

The most intense stress typically occurs after the procedure, especially following a positive pregnancy test and before ultrasound confirmation. This period, which lasts at least 3-4 weeks, is characterized by considerable uncertainty, as neither patients nor healthcare providers have reliable tools to determine pregnancy viability, assess early development, or accurately predict pregnancy progression. An individualized assessment of the probability of live birth after a positive pregnancy test could provide clinically meaningful information during this period and potentially improve counseling and management of patient expectations.

Serum beta-hCG is one of the earliest measurable biomarkers following embryo implantation and has long been recognized as an important prognostic marker of early pregnancy outcome. Both the absolute concentration of beta-HCG and its subsequent rate of increase have been associated with pregnancy viability and live birth following embryo transfer.

Investigators plan to use a machine-learning system to collect and analyze retrospective clinical data. Beta-HCG values from this dataset were collected at very early stages of pregnancy (around aspiration days +14 and 16, and post-FET days 9 and 11).

Patients were advised to have blood drawn for beta-HCG measurement 14 days after oocyte aspiration or insemination, followed by a second measurement two days later. For FET, measurements were taken 9 days after blastocyst transfer (or the corresponding day for cleavage-stage embryos) and two days afterward. Due to scheduling constraints, such as weekends, actual measurements may have occurred one day earlier or later, or several days apart. The dataset included the exact dates of each blood draw, allowing precise calculation of the interval between measurements for analysis.

ART outcomes were primarily collected through direct patient reporting of events, including adverse pregnancy outcomes or live birth; for patients who did not report the outcomes, clinic staff conducted follow-up calls to ensure complete follow-up.

This study is an observational retrospective-prospective cohort study for development and validation of an AI (artificial intelligence) - based prognostic model predicting live birth after ART.

The retrospective phase will use existing clinical data from patients who underwent ART procedures at the BetaPlus Center between January 2017 and 31.12.2025.

The prospective phase will include consecutive patients undergoing ART after model development in both BetaPlus Center and Clinical University Hospital in Rijeka. These patients will be followed to assess pregnancy outcomes, enabling external validation of the model.

The study is observational in nature. No interventions, treatment modifications, or randomization will be performed as part of this research. Clinical management will follow standard operating procedures (SOP) independent of model predictions.

Tipo di studio

Osservativo

Iscrizione (Stimato)

2200

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

      • Rijeka, Croazia
        • Reclutamento
        • Clinical Hospital Center
        • Contatto:
      • Zagreb, Croazia, 10000
        • Reclutamento
        • BetaPlus Center for Reproductive Medicine
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 45 anni (Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Femmina

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Participants will be women undergoing ART at the BetaPlus Center and, during the prospective validation phase, at the Clinical University Hospital in Rijeka, Croatia. The study population will include patients undergoing IVF/ICSI, FET, or IUI.

Descrizione

Inclusion Criteria:

  • Women who underwent ART procedures (IUI, IVF/ICSI, or FET) using homologous oocytes.
  • Availability of at least one positive early serum beta-HCG measurement after aspiration, FET, or insemination (beta-HCG >10 mIU/mL).
  • Availability of the pregnancy outcome.
  • Availability of relevant patient characteristics and clinical variables required for predictive modeling.
  • For embryo-transfer cycles, availability of information on embryo developmental stage and number of embryos transferred where applicable.
  • For the prospective validation cohort, written informed consent.

Exclusion Criteria

  • Missing beta-HCG measurements critical for model input.
  • Missing key demographic or clinical variables required for predictive modeling.
  • Missing ART treatment protocol where required for the model.
  • Missing pregnancy outcomes.
  • Multiple pregnancy, hydatidiform mole, heterotopic pregnancy, and ectopic pregnancy will be excluded from the primary live-birth analysis but will be described separately and, where sample size permits, evaluated as secondary adverse pregnancy outcomes.
  • Non-consent for prospective participation in validation.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: COHORT
  • Prospettive temporali: OTHER

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
ART pregnancies with positive beta-hCG

Patients with a positive serum beta-hCG measurement following ART, including IVF, FET, and IUI. Participants will be followed to assess pregnancy outcomes, including live birth, biochemical pregnancy, and early pregnancy loss.

A machine-learning prognostic model using early serum beta-hCG measurements and patient, embryo, and treatment characteristics to predict live birth and early adverse pregnancy outcomes following assisted reproductive treatment.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Live birth following ART
Lasso di tempo: From positive pregnancy test until delivery.

Delivery of a live infant at ≥24 weeks of gestation.

From positive pregnancy test until delivery.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Biochemical pregnancy following ART
Lasso di tempo: From the first positive serum beta-hCG measurement until biochemical pregnancy resolution.

A pregnancy characterized by a positive serum beta-hCG test followed by bleeding or pregnancy loss without ultrasound confirmation of a clinical pregnancy.

From the first positive serum beta-hCG measurement until biochemical pregnancy resolution.
Early Pregnancy Loss following ART
Lasso di tempo: From clinical pregnancy confirmation until 12 weeks of gestation.

Pregnancy loss occurring before 12 weeks of gestation, excluding biochemical pregnancy, ectopic pregnancy, heterotopic pregnancy, and hydatidiform mole.

From clinical pregnancy confirmation until 12 weeks of gestation.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Romana Dmitrovic, BetaPlus Center for Reproductive Medicine

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 gennaio 2026

Completamento primario (Stimato)

31 dicembre 2026

Completamento dello studio (Stimato)

30 settembre 2027

Date di iscrizione allo studio

Primo inviato

28 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

28 settembre 2026

Primo Inserito (Effettivo)

2 ottobre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

7 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 ottobre 2026

Ultimo verificato

1 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • PK 1.1.12.0074
  • PK 1.1.12.0074 (Altro numero di sovvenzione/finanziamento: HAMAG BICRO)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Descrizione del piano IPD

De-identified individual participant data underlying the results of this study will be made available upon reasonable request. The shared dataset will include the clinical and treatment variables necessary to reproduce or further investigate the study findings, including relevant beta-hCG measurements, timing of measurements, ART treatment characteristics, and pregnancy outcomes.

Data will not include names, contact information, medical record numbers, or other directly identifying information.

Periodo di condivisione IPD

After publication and for 5 years thereafter

Criteri di accesso alla condivisione IPD

Data will be available to qualified researchers, subject to applicable ethical, legal, and institutional requirements

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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