Analýza EKG pomocí AI pomocí softwaru Willem™ u vysoce rizikových kardiaků (WILLEM) (WILLEM)
Vyhodnocení elektrokardiografických dat od vysoce rizikových kardiaků pomocí softwaru umělé inteligence Willem™ na úrovni kardiologa. Soud WILLEM.
WILLEM is a multi-center, prospective and retrospective cohort study.
The study will assess the performance of a cloud-based and AI-powered ECG analysis platform, named Willem™, developed to detect arrhythmias and other abnormal cardiac patterns. The main questions it aims to answer are:
- A new AI-powered ECG analysis platform can automatice the classification and prediction of cardiac arrhythmic episodes at a cardiologist level.
- This AI-powered ECG analysis can delay or even avoid harmful therapies and severe cardiac adverse events such as sudden death.
The prerequisites for inclusion of patients will be the availability of at least one ECG record in raw data, along with patient clinical data and evolution data after more than 1-year follow-up.
Cardiac electrical signals from multiple medical devices will be collected by cardiology experts after obtaining the informed consent. Every cardiac electrical signal from every subject will be reviewed by a board-certified cardiologist to label the arrhythmias and patterns recorded in those tracings. In order to obtain tracings of relevant information, >95% of the subjects enrolled will have rhythm disorders or abnormal ECG's patterns at the time of enrollment.
Přehled studie
Postavení
Detailní popis
The WILLEM study is an investigator-initiated, multicenter, observational trial aiming to validate a cloud-based AI-powered ECG analysis platform to early diagnose and predict the behavior of cardiac abnormalities and cardiac diseases from patients admitted to cardiovascular units. Model-derived diagnosis will be compared with cardiology expert's diagnosis in a test dataset. Clinical outcomes will be included to assess model prediction capabilities: sensitivity, specificity and accuracy. In this observational study, patients will be randomly divided into two groups: (1) a training group to design new methodologies and algorithms; and (2) a test group to evaluate performance of methodologies aiming to avoid overfitting.
Willem™ AI-powered ECG analysis platform supports the analysis of cardiac electrical signals ≥ 10 seconds onwards obtained from devices in-clinic (E.g., 12-lead ECG devices at hospitals or primary care, telemetries, monitors) and at-home or telemedicine interfaces (E.g., Holter devices, event recorders, 6, 3, 2, 1-lead ECG wearables, textile electrodes and patches for mobile cardiac telemetry).
Typ studie
Zápis (Odhadovaný)
Kontakty a umístění
Studijní kontakt
- Jméno: Manuel Marina-Breysse, MSc, MD
- Telefonní číslo: +34618103160
- E-mail: manuel.marina@idoven.ai
Studijní záloha kontaktů
- Jméno: José María Lillo, PhD
- E-mail: c@idoven.ai
Studijní místa
-
-
Provincie Groningen
-
Groningen, Provincie Groningen, Holandsko, 9713 GZ
- Dokončeno
- University Medical Center Groningen
-
-
-
-
Barcelona
-
Barcelona, Barcelona, Španělsko, 08950
- Dokončeno
- Hospital Sant Joan de Déu
-
-
Ciudad Real
-
Ciudad Real, Ciudad Real, Španělsko, 13005
- Dokončeno
- Hospital General Universitario de Ciudad Real
-
-
La Coruña
-
A Coruña, La Coruña, Španělsko, 15006
- Dokončeno
- Complejo Hospitalario Universitario A Coruña
-
-
Madrid
-
Madrid, Madrid, Španělsko, 28822
- Dokončeno
- Hospital Universitario del Henares
-
Madrid, Madrid, Španělsko, 28400
- Dokončeno
- Hospital Universitario General de Villalba
-
Madrid, Madrid, Španělsko, 28040
- Dokončeno
- Hospital Clínico San Carlos
-
Madrid, Madrid, Španělsko, 28222
- Dokončeno
- Hospital Universitario Puerta de Hierro
-
-
Murcia
-
Murcia, Murcia, Španělsko, 30120
- Dokončeno
- Hospital Virgen de Arrixaca
-
-
Navarre
-
Pamplona, Navarre, Španělsko, 31008
- Nábor
- Clínica Universitaria Navarra
-
Kontakt:
- Manuel García de Yébenes Castro, MD
-
Vrchní vyšetřovatel:
- Manuel García de Yébenes Castro
-
-
Santa Cruz de Tenerife
-
Santa Cruz de Tenerife, Santa Cruz de Tenerife, Španělsko, 38010
- Dokončeno
- Hospital Universitario Nuestra Señora de Candelaria
-
-
Valencia
-
Valencia, Valencia, Španělsko, 46026
- Dokončeno
- Hospital Universitario y Politécnico La Fe
-
-
Vizcaya
-
Bilbao, Vizcaya, Španělsko, 48013
- Nábor
- Hospital Universitario de Basurto
-
Kontakt:
- Alain García Olea, MD
-
Vrchní vyšetřovatel:
- Alain García Olea
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Metoda odběru vzorků
Studijní populace
Patients recorded with a mid to long-term ECG device according to guidelines. ECG data (ECG must have been recorded according to the technical standards for the safety and essential performance of medical electrical equipment defined in EN 60601-2-47:2015.): 12-lead ECGs including rest electrocardiograms, stress ECG Test (exercise Electrocardiogram or treadmill test), Holter devices, long-duration Holter devices, event recorders, insertable cardiac monitors, 6,3,2,1-lead ECG wearables, textile electrodes and patches, smartwatches, cardiac monitors, cardiac telemetries, hemodynamic and electrophysiology recording system (i.e., polygraphs), automatic external defibrillator (AED), semi-automatic defibrillator (DESA), home telemonitoring systems and other similar devices.
Popis
Inclusion Criteria:
- Patient presenting relevant cardiac arrhythmias and cardiac patterns (including supraventricular tachycardias, abnormal ECG patterns, ventricular tachycardias, ventricular fibrillation, pulseless electrical activity or asystole among others) that have been recorded with at least one short-term ECG medical device according to guidelines with ≥1 signal-channel.
- Patient with suspected or diagnosed acute/chronic cardiac diseases (including patients with heart failure, patients with history of cardiac arrhythmias, patients with probable coronary artery diseases, patients with cardiomyopathies, patients with pacemakers or implantable cardioverter-defibrillators (ICD), patients with indication of pacemaker or ICD in current or short-term phase, patients participating in other interventional clinical investigation, patients with hemodynamic instability or acute coronary syndromes, pregnant patients, patients with cancer and chemotherapy, patients with life-expectancy lower than 24 months, patients with in or out-of-hospital cardiac arrest with ventricular fibrillation as first documented rhythm).
- At least one ECG tracing that can be exported in raw data.
- Signed informed consent. Patients unable to consent, it will be requested to an authorized relative.
Exclusion Criteria:
- Unwillingness or inability to sign study written informed consent.
- Unavailable or suboptimal quality of the electrocardiographic signal in raw data.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Observační modely: COHORT
- Časové perspektivy: RETROSPECTIVE
Kohorty a intervence
Skupina / kohorta |
Intervence / Léčba |
|---|---|
|
Train group
Consecutive patients admitted to the hospital due to cardiac disorders (retrospective and prospective) with at least one relevant ECG record >10 sec in raw data will be used to design new methodologies and algorithms for cardiac patterns recognition. |
ECG recording and processing by AI platform |
|
Test group
Consecutive patients admitted to the hospital due to cardiac disorders (retrospective and prospective) with at least one relevant ECG record >10 sec in raw data will be used to evaluate performance of methodologies aiming to avoid overfitting. Every 10 patients included in Train group; a new patient is included in the test group. |
ECG recording and processing by AI platform |
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Detection of cardiac arrhythmias and cardiac patterns in the electrocardiographic signals
Časové okno: real time to 7 minutes
|
Willem™ heart rhythm and cardiac pattern performance compared to standard manually performed cardiologist diagnosis. |
real time to 7 minutes
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Survival at follow-up
Časové okno: 1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
Patients alive at the time of follow-up |
1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
|
Major Adverse Cardiovascular and Cerebrovascular Events (MACCE)
Časové okno: 1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
MACCE rates defined as cardiovascular and cerebrovascular events during the follow up |
1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
|
Re-hospitalization
Časové okno: 1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
Number of Re-hospitalizations during the follow up. |
1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
|
Change in quality of life
Časové okno: 1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
European Quality of Life-5 Dimensions (EQ-5D) index an utility scores anchored at 0 for death and 1 for perfect health. |
1 year after the first ECG (prospective patients) or after patient enrollment (retrospective patients)
|
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Vyšetřovatelé
- Vrchní vyšetřovatel: María De La Parte, MD, Idoven 1903 S.L.
Publikace a užitečné odkazy
Obecné publikace
- Lillo-Castellano JM, Gonzalez-Ferrer JJ, Marina-Breysse M, Martinez-Ferrer JB, Perez-Alvarez L, Alzueta J, Martinez JG, Rodriguez A, Rodriguez-Perez JC, Anguera I, Vinolas X, Garcia-Alberola A, Quintanilla JG, Alfonso-Almazan JM, Garcia J, Borrego L, Canadas-Godoy V, Perez-Castellano N, Perez-Villacastin J, Jimenez-Diaz J, Jalife J, Filgueiras-Rama D. Personalized monitoring of electrical remodelling during atrial fibrillation progression via remote transmissions from implantable devices. Europace. 2020 May 1;22(5):704-715. doi: 10.1093/europace/euz331.
- Quartieri F, Marina-Breysse M, Pollastrelli A, Paini I, Lizcano C, Lillo-Castellano JM, Grammatico A. Artificial intelligence augments detection accuracy of cardiac insertable cardiac monitors: Results from a pilot prospective observational study. Cardiovasc Digit Health J. 2022 Aug 4;3(5):201-211. doi: 10.1016/j.cvdhj.2022.07.071. eCollection 2022 Oct.
- Lillo-Castellano JM, Marina-Breysse M, Gomez-Gallanti A, Martinez-Ferrer JB, Alzueta J, Perez-Alvarez L, Alberola A, Fernandez-Lozano I, Rodriguez A, Porro R, Anguera I, Fontenla A, Gonzalez-Ferrer JJ, Canadas-Godoy V, Perez-Castellano N, Garofalo D, Salvador-Montanes O, Calvo CJ, Quintanilla JG, Peinado R, Mora-Jimenez I, Perez-Villacastin J, Rojo-Alvarez JL, Filgueiras-Rama D. Safety threshold of R-wave amplitudes in patients with implantable cardioverter defibrillator. Heart. 2016 Oct 15;102(20):1662-70. doi: 10.1136/heartjnl-2016-309295. Epub 2016 Jun 13.
- Martinez-Selles M, Marina-Breysse M. Current and Future Use of Artificial Intelligence in Electrocardiography. J Cardiovasc Dev Dis. 2023 Apr 17;10(4):175. doi: 10.3390/jcdd10040175.
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- 1903/21
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .