- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07644715
AI-powered ECG Analysis for Deadly Arrhythmias and ICI Myocarditis (ELDORA)
Efficient Deep Learning Approaches for the Rapid and Interpretable Detection of Deadly Arrhythmias in ECG Data
Studieoversigt
Status
Detaljeret beskrivelse
"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."
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Joe-Elie Salem, MD-PhD
- Telefonnummer: 0033142178535
- E-mail: joe-elie.salem@aphp.fr
Undersøgelse Kontakt Backup
- Navn: Edi Prifti, PhD
- Telefonnummer: +33 1 48 02 55 20
- E-mail: edi.prifti@ird.fr
Studiesteder
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Paris, Frankrig, 75013
- Rekruttering
- CIC-2503
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
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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
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: AUC
Tidsramme: Up to study completion (anticipated 48 months)
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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.
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Up to study completion (anticipated 48 months)
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Creation and harmonization of the ECG Insight database across participating ECG cohorts
Tidsramme: Up to study completion (anticipated 48 months)
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Consolidation, anonymization/de-identification, standardization and secure integration of ECG waveforms, annotations and clinical metadata from participating cohorts into ECGInsight.
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Up to study completion (anticipated 48 months)
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Performance of ECG digitization/standardization toolkit for heterogeneous ECG data : Accuracy
Tidsramme: Up to study completion (anticipated 48 months)
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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.
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Up to study completion (anticipated 48 months)
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Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Sensitivity
Tidsramme: Up to study completion (anticipated 48 months)
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Sensitivity of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
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Up to study completion (anticipated 48 months)
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Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Specificity
Tidsramme: Up to study completion (anticipated 48 months
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Specificity of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
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Up to study completion (anticipated 48 months
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Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: F1 Score
Tidsramme: Up to study completion (anticipated 48 months)
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F1 score of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
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Up to study completion (anticipated 48 months)
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Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Accuracy
Tidsramme: Up to study completion (anticipated 48 months)
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Accuracy of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
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Up to study completion (anticipated 48 months)
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Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: Regression / Agreement metrics
Tidsramme: Up to study completion (anticipated 48 months)
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Regression / Agreement metrics of the prediction models for TdP/long QT risk and ICI-myocarditis diagnosis, prognosis, and risk prediction.
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Up to study completion (anticipated 48 months)
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Samarbejdspartnere og efterforskere
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CIC2503-26-05
Plan for individuelle deltagerdata (IPD)
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Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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