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AI-powered ECG Analysis for Deadly Arrhythmias and ICI Myocarditis (ELDORA)

8 juni 2026 bijgewerkt door: Joe Elie Salem, Groupe Hospitalier Pitie-Salpetriere

Efficient Deep Learning Approaches for the Rapid and Interpretable Detection of Deadly Arrhythmias in ECG Data

ELDORA is a non-interventional observational data-science study aiming to develop and validate clinical-grade artificial intelligence tools applied to electrocardiogram (ECG) data. The project will standardize heterogeneous ECGs, create the ECGInsight harmonized database, and train interpretable models for life-threatening arrhythmia risk prediction, especially Torsades-de-Pointes/long QT syndrome and immune checkpoint inhibitor (ICI)-induced myocarditis. The project uses existing and ongoing national and international ECG cohorts with de-identified clinical metadata; AI outputs are intended for research/model development and are not used to drive patient care during the study.

Studie Overzicht

Gedetailleerde beschrijving

"ELDORA (Efficient Deep Learning Approaches for the Rapid and Interpretable Detection of Deadly Arrhythmias in ECG Data) is an observational, non-interventional project focused on ECG-based artificial intelligence. Its overarching objective is to develop and optimize clinical-grade AI-powered tools for: (1) digitizing, standardizing and analyzing heterogeneous ECG signals, including real-life analog/paper-derived and digital recordings; and (2) supporting clinical decision research for two sudden-cardiac-arrest-prone conditions: Torsades-de-Pointes (TdP) risk prediction in established long QT syndrome, whether congenital or drug-induced, and diagnosis, prognosis and risk prediction for immune checkpoint inhibitor-induced myocarditis.

The project will consolidate diverse ECG and clinical datasets into ECGInsight, a harmonized database planned to include approximately 49 national and international ECG cohorts, around 127,000 subjects and up to about 10 million 10-second ECG equivalents. Cohorts cover a broad spectrum of health states and cardiovascular conditions, including healthy volunteers, congenital and drug-induced long QT/TdP populations, cancer patients treated with immune checkpoint inhibitors with or without myocarditis, heart transplant, diabetes, obesity and hormonal phenotyping cohorts. Data include raw ECG waveforms, automatic and expert annotations, scanned paper ECGs where applicable, demographics, clinical characteristics, laboratory results, drug exposure and hormono-metabolic assessments near the time of ECG acquisition.

Data curation will include mapping of cohort variables and clinical concepts into an ELDORA glossary, using controlled terminologies where appropriate, including ICD-10, MedDRA, OMOP and ATC for drug exposure. ECGs will be standardized using the project toolkit and integrated in a secure, GDPR-compliant infrastructure. Access is intended to be controlled and limited to approved researchers/clinicians under the project governance. The study involves no treatment allocation, no investigational medicinal product and no direct AI-driven change to patient care. Model performance will be evaluated using standard classification and regression metrics, including AUC, sensitivity, specificity, F1 score, accuracy, MAE, RMSE, R2 and Bland-Altman analyses, as appropriate to each task."

Studietype

Observationeel

Inschrijving (Geschat)

127000

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

      • Paris, Frankrijk, 75013
        • Werving
        • CIC-2503

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind
  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Ja

Bemonsteringsmethode

Niet-waarschijnlijkheidssteekproef

Studie Bevolking

Subjects from existing and ongoing ECG cohorts contributing to ECGInsight, including healthy volunteers and patients with cardiovascular diseases, cancer/ICI exposure, LQT/TdP and ICI-myocarditis-relevant phenotypes.

Beschrijving

Inclusion Criteria:

  • subjects included in participating existing or ongoing ECG cohorts made available to ECGInsight
  • availability of ECG data (digital waveform or scanned/paper ECG suitable for digitization) and relevant clinical/demographic metadata
  • data use permitted by applicable ethical, regulatory, contractual and GDPR requirements.

Exclusion Criteria:

  • datasets or individual records for which required approvals, data-sharing agreements, de-identification/anonymization, or minimum ECG/metadata quality requirements are not met. No interventional study treatment is assigned.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

Cohorten en interventies

Groep / Cohort
A unified dataset (ECGinsight) comprising at least 10 millions ECG
A unified dataset (ECGinsight) comprising at least 10 millions ECG spanning from multiple international setting and including healthy volunteers, LQT/TdP, cancer/ICI myocarditis, heart transplant, diabetes, obesity, hormonal and patients with cardiovascular comorbidities and events

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: AUC
Tijdsspanne: Up to study completion (anticipated 48 months)
Model discrimination performance assessed using the Area Under the Receiver Operating Characteristic Curve (AUC) for prediction of torsade de pointes (TdP)/long QT risk and immune checkpoint inhibitor (ICI)-myocarditis diagnosis, prognosis, and risk.
Up to study completion (anticipated 48 months)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Creation and harmonization of the ECG Insight database across participating ECG cohorts
Tijdsspanne: Up to study completion (anticipated 48 months)
Consolidation, anonymization/de-identification, standardization and secure integration of ECG waveforms, annotations and clinical metadata from participating cohorts into ECGInsight.
Up to study completion (anticipated 48 months)
Performance of ECG digitization/standardization toolkit for heterogeneous ECG data : Accuracy
Tijdsspanne: Up to study completion (anticipated 48 months)
Accuracy of ECG digitization and standardization tools for conversion of analog/paper-derived and digital ECG data into analysis-ready formats, assessed by comparison with reference ECG signals.
Up to study completion (anticipated 48 months)
Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Sensitivity
Tijdsspanne: Up to study completion (anticipated 48 months)
Sensitivity of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
Up to study completion (anticipated 48 months)
Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Specificity
Tijdsspanne: Up to study completion (anticipated 48 months
Specificity of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
Up to study completion (anticipated 48 months
Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: F1 Score
Tijdsspanne: Up to study completion (anticipated 48 months)
F1 score of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
Up to study completion (anticipated 48 months)
Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Accuracy
Tijdsspanne: Up to study completion (anticipated 48 months)
Accuracy of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
Up to study completion (anticipated 48 months)
Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Regression / Agreement metrics
Tijdsspanne: Up to study completion (anticipated 48 months)
Regression / Agreement metrics of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
Up to study completion (anticipated 48 months)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 januari 2026

Primaire voltooiing (Geschat)

31 december 2029

Studie voltooiing (Geschat)

31 december 2029

Studieregistratiedata

Eerst ingediend

2 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

8 juni 2026

Eerst geplaatst (Werkelijk)

12 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

12 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

8 juni 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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