- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico 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
Descripción general del estudio
Estado
Descripción detallada
"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."
Tipo de estudio
Inscripción (Estimado)
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Joe-Elie Salem, MD-PhD
- Número de teléfono: 0033142178535
- Correo electrónico: joe-elie.salem@aphp.fr
Copia de seguridad de contactos de estudio
- Nombre: Edi Prifti, PhD
- Número de teléfono: +33 1 48 02 55 20
- Correo electrónico: edi.prifti@ird.fr
Ubicaciones de estudio
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Paris, Francia, 75013
- Reclutamiento
- CIC-2503
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Método de muestreo
Población de estudio
Descripción
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.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
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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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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Performance of AI models for ECG-based prediction/diagnosis of life-threatening arrhythmia conditions: AUC
Periodo de tiempo: 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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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Creation and harmonization of the ECG Insight database across participating ECG cohorts
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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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Colaboradores e Investigadores
Patrocinador
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedad del sistema de conducción cardíaca
- Enfermedades cardiovasculares
- Procesos Patológicos
- Enfermedades cardíacas
- Anomalías congénitas
- Anomalías cardiovasculares
- Defectos Cardíacos Congénitos
- Enfermedades y anomalías congénitas, hereditarias y neonatales
- Condiciones Patológicas, Signos y Síntomas
- Arritmias Cardiacas
- Síndrome de QT largo
Otros números de identificación del estudio
- CIC2503-26-05
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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