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Recruiting NCT05829993

NCT05829993 Development of an Artificial Intelligence Algorithm to Detect Pathological Repolarization Disorders on the ECG and the Risk of Ventricular Arrhythmias

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Clinical Trial Summary
NCT ID NCT05829993
Status Recruiting
Phase
Sponsor Assistance Publique - Hôpitaux de Paris
Condition Cardiac Disease
Study Type OBSERVATIONAL
Enrollment 5,000 participants
Start Date 2023-11-28
Primary Completion 2027-05-28

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

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What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 5,000 participants in total. It began in 2023-11-28 with a primary completion date of 2027-05-28.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Torsades de Pointes (TdP) are potentially fatal ventricular arrhythmias that are promoted by prolonged ventricular repolarization (Long QT, LQT). The different forms of LQT result from inhibition of cardiac potassium currents (IKr and IKs) or activation of a late sodium current (INaL). These alterations may be either congenital (3 types: cLQT-1: IKs, cLQT-2: IKr, cLQT-3: INaL) or drug-induced (diLQT, via inhibition of IKr). More than 100 medications have received marketing authorization despite a known risk of TdP, due to a favorable benefit-risk ratio (e.g., hydroxychloroquine). QTc, which represents the duration of ventricular repolarization (in milliseconds) - defined as the time from the beginning of the QRS complex to the end of the T wave, corrected for heart rate - is prolonged in all forms of LQT. Specific T-wave abnormalities, depending on the altered ion currents, have been described and can help differentiate the various types of congenital or drug-induced LQT. However, screening for LQT and TdP risk, both at the individual and population levels, currently relies mainly on isolated QTc evaluation and genetic testing, which often takes considerable time to return. Thus, limiting ECG analysis to QTc measurement alone offers low predictive value, as the ECG contains a wealth of additional information beyond a single interval. The investigator recently demonstrated that artificial intelligence (AI)-based ECG analysis using deep-learning convolutional neural networks can detect more discriminative features of the ECG for predicting the type of LQT and the risk of TdP, going beyond QTc alone. Using these techniques, the investigator developed a model with probabilistic modules capable of: predicting TdP risk, identifying LQT subtypes (scores ranging from 0 to 100%), and quantitatively measuring ECG parameters such as QTc, heart rate, PR, and QRS duration. The objective of this project is to prospectively validate our model in real-world conditions across various departments within AP-HP, for: Automatic measurement of QTc, and Identification and classification of LQT types and TdP risk.

Eligibility Criteria

Inclusion Criteria: * Age ≥ 18 * Patients or subjects taken care in recruiting centres for which an ECG is indicated * No opposition to participation in the study Exclusion Criteria: * Medical contraindication for ECG * Subjects with pacemaker-driven QRS

Contact & Investigator

Central Contact

Joe-Elie SALEM, PU-PH

✉ joe-elie.salem@aphp.fr

📞 0033 1 42 17 85 35

Principal Investigator

Joe-Elie SALEM, PU-PH

PRINCIPAL INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Frequently Asked Questions

Who can join the NCT05829993 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Cardiac Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05829993 currently recruiting?

Yes, NCT05829993 is actively recruiting participants. Contact the research team at joe-elie.salem@aphp.fr for enrollment information.

Where is the NCT05829993 trial being conducted?

This trial is being conducted at Paris, France.

Who is sponsoring the NCT05829993 clinical trial?

NCT05829993 is sponsored by Assistance Publique - Hôpitaux de Paris. The principal investigator is Joe-Elie SALEM, PU-PH at Assistance Publique - Hôpitaux de Paris. The trial plans to enroll 5,000 participants.

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