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Algorithm Development Through AI for the Triage of Stroke Patients in the Ambulance With EEG (AI-STROKE)

27 juin 2022 mis à jour par: Jonathan Coutinho, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Algorithm Development Through Artificial Intelligence for the Triage of Stroke Patients in the Ambulance With Electroencephalography

Endovascular thrombectomy (EVT) enormously improves the prognosis of patients with large vessel occlusion (LVO) stroke, but its effect is highly time-dependent. Direct presentation of patients with an LVO stroke to an EVT-capable hospital reduces onset-to-treatment time by 40-115 minutes and thereby improves clinical outcome. Electroencephalography (EEG) may be a suitable prehospital stroke triage instrument for identifying LVO stroke, as differences have been found between EEG recordings of patients with an LVO stroke and those of suspected acute ischemic stroke patients with a smaller or no vessel occlusion. The investigators expect EEG can be performed in less than five minutes in the prehospital setting using a dry electrode EEG cap. An automatic LVO-detection algorithm will be the key to reliable, simple and fast interpretation of EEG recordings by ambulance paramedics. The primary objective of this study is to develop one or more novel AI-based algorithms (the AI-STROKE algorithms) with optimal diagnostic accuracy for identification of LVO stroke in patients with a suspected acute ischemic stroke in the prehospital setting, based on ambulant EEG data.

Aperçu de l'étude

Statut

Recrutement

Les conditions

Intervention / Traitement

Description détaillée

RATIONALE

Large vessel occlusion (LVO) stroke causes around 30% of acute ischemic strokes (AIS) and is associated with severe deficits and poor neurological outcomes. Endovascular thrombectomy (EVT) enormously improves the prognosis of patients with LVO stroke, but its effect is highly time-dependent. Because of its complexity and required resources, EVT can be performed in selected hospitals only. In the Netherlands, approximately half of the EVT-eligible patients are initially admitted to a hospital incapable of performing EVT, and - once it has been ascertained that the patient requires EVT - the patient needs to be transported a second time by ambulance to an EVT-capable hospital. Interhospital transfer leads to a treatment delay of 40-115 minutes, which decreases the absolute chance of a good outcome of the patient by 5-15%. To solve this issue, a prehospital stroke triage instrument is needed, which reliably identifies LVO stroke in the ambulance, so that these patients can be brought directly to an EVT-capable hospital. Electroencephalography (EEG) may be suitable for this purpose, since it shows almost instantaneous changes in response to cerebral blood flow reduction. Moreover, significant differences between EEGs of patients with an LVO stroke and those of suspected AIS patients with a smaller or no vessel occlusion have been found. A dry electrode EEG cap enables ambulance paramedics to perform an EEG in the prehospital setting, with significant reduced preparation time compared to conventional wet electrode EEG. An automatic LVO-detection algorithm will be the key to reliable, simple and fast interpretation of the EEG by paramedics, enabling direct admission of suspected AIS patients to the right hospital.

HYPOTHESIS

An EEG-based algorithm, developed with artificial intelligence (AI), will have sufficiently high diagnostic accuracy to be used by ambulance paramedics for prehospital LVO detection.

OBJECTIVE

The primary objective of this study is to develop one or more novel AI-based algorithms (the AI-STROKE algorithms) with optimal diagnostic accuracy for identification of LVO stroke in patients with a suspected AIS in the prehospital setting, based on ambulant EEG data.

STUDY DESIGN

AI-STROKE is an investigator-initiated, multicenter, diagnostic test accuracy study.

STUDY POPULATION

Part A: Adult patients with a (suspected) AIS, in the prehospital setting. Part B: Adult patients with a (suspected) AIS, in the in-hospital setting.

INTERVENTION

A single EEG measurement with a dry electrode cap (approximately 2 minutes recording duration) will be performed in each patient. In addition, clinical and radiological data will be collected. EEG data will be acquired with a CE approved portable dry electrode EEG device.

MAIN END POINTS

Primary end point: Based on the EEG data, and using the final diagnosis based on CT angiography data established by an adjudication committee as the gold standard, one or more novel AI-based EEG algorithms (the AI-STROKE algorithms) will be developed with maximal diagnostic accuracy (i.e. area under the receiver operating characteristic curve; AUC) to identify patients with an LVO stroke of the anterior circulation in a population of patients with suspected AIS.

Secondary end points:

  • AUC, sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the AI-STROKE algorithms based on ambulant EEG for diagnosis of LVO of the anterior circulation in suspected AIS patients in the prehospital setting;
  • AUC, sensitivity, specificity, PPV and NPV of existing EEG algorithms based on ambulant EEG for diagnosis of LVO stroke of the anterior circulation in suspected AIS patients in the prehospital setting;
  • AUC, sensitivity, specificity, PPV and NPV of existing and newly developed EEG algorithms based on ambulant EEG for detection of LVO stroke of the posterior circulation, intracerebral hemorrhage, transient ischemic attack, and stroke mimics;
  • Technical and logistical feasibility (e.g. in terms of EEG channel reliability) of paramedics performing ambulant EEG in patients with a suspected AIS in the prehospital setting.

Type d'étude

Interventionnel

Inscription (Anticipé)

1192

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

  • Pays-Bas
    • Noord-Holland
      • Amsterdam, Noord-Holland, Pays-Bas, 1105AZ
        • Recrutement
        • Amsterdam University Medical Centers, location AMC
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Suspected AIS, as assessed by the attending ambulance paramedic, or a known LVO stroke;
  • Onset of symptoms or last seen well < 24 hours before EEG acquisition;
  • Age of 18 years or older;
  • Written informed consent by patient or legal representative (deferred).

Exclusion Criteria:

  • Skin defect or active infection of the scalp in the area of the electrode cap placement;
  • (Suspected) COVID-19 infection.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Diagnostique
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Dry electrode cap EEG
All patients that are included in the study will undergo a dry electrode electroencephalography (EEG).
Test diagnostique: Dry electrode EEG
A single dry electrode electroencephalography (EEG) will be performed in each patient that is included in this study. For this purpose the Waveguard touch dry electrode EEG cap and compatible eego mini amplifier (ANT Neuro B.V., Hengelo, Netherlands) are used to record and amplify the EEG signal, respectively. Both products are CE marked as medical devices in the European Union and will be used within the intended use as described in the user manuals.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
One or more novel AI-based EEG algorithms based on dry electrode EEG-data with optimal diagnostic accuracy for LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
One or more novel artificial intelligence (AI) based electroencephalography (EEG) algorithms (the AI-STROKE algorithms) with maximal diagnostic accuracy to identify patients with an large vessel occlusion of the anterior circulation (LVO-a) in a population of patients with suspected acute ischemic stroke. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
AUC of the AI-STROKE algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Area under the receiver operating characteristic curve (AUC) of the AI-STROKE algorithms based on ambulant electroencephalography (EEG) for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Sensitivity of the AI-STROKE algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Sensitivity of the AI-STROKE algorithms based on ambulant electroencephalography (EEG) for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Specificity of the AI-STROKE algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Specificity of the AI-STROKE algorithms based on ambulant electroencephalography (EEG) for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
PPV of the AI-STROKE algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Positive predictive value (PPV) of the AI-STROKE algorithms based on ambulant electroencephalography (EEG) for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
NPV of the AI-STROKE algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Negative predictive value (NPV) of the AI-STROKE algorithms based on ambulant electroencephalography (EEG) for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
AUC of existing EEG algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Area under the receiver operating characteristic curve (AUC) of existing electroencephalography (EEG) algorithms based on ambulant EEG for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Sensitivity of existing EEG algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Sensitivity of existing electroencephalography (EEG) algorithms based on ambulant EEG for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Specificity of existing EEG algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Specificity of existing electroencephalography (EEG) algorithms based on ambulant EEG for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
PPV of existing EEG algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Positive predictive value (PPV) of existing electroencephalography (EEG) algorithms based on ambulant EEG for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
NPV of existing EEG algorithms for diagnosis of LVO-a
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Negative predictive value (NPV) of existing electroencephalography (EEG) algorithms based on ambulant EEG for diagnosis of large vessel occlusion of the anterior circulation (LVO-a) in suspected acute ischemic stroke patients in the prehospital setting. For each patient a single dry electrode electroencephalography (EEG) will be performed and the presence or absence of an LVO-a will be assessed based on CT angiography data acquired at the emergency department.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
AUC of existing and newly developed EEG algorithms for detection of LVO-p, intracerebral hemorrhage, transient ischemic attack, and stroke mimics
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Area under the receiver operating characteristic curve (AUC) of existing and newly developed electroencephalography (EEG) algorithms based on ambulant EEG for detection of an large vessel occlusion of the posterior circulation (LVO-p), intracerebral hemorrhage, transient ischemic attack, and stroke mimics.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Sensitivity of existing and newly developed EEG algorithms for detection of LVO-p, intracerebral hemorrhage, transient ischemic attack, and stroke mimics
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Sensitivity of existing and newly developed electroencephalography (EEG) algorithms based on ambulant EEG for detection of an large vessel occlusion of the posterior circulation (LVO-p), intracerebral hemorrhage, transient ischemic attack, and stroke mimics.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Specificity of existing and newly developed EEG algorithms for detection of LVO-p, intracerebral hemorrhage, transient ischemic attack, and stroke mimics
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Specificity of existing and newly developed electroencephalography (EEG) algorithms based on ambulant EEG for detection of an large vessel occlusion of the posterior circulation (LVO-p), intracerebral hemorrhage, transient ischemic attack, and stroke mimics.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
PPV of existing and newly developed EEG algorithms for detection of LVO-p, intracerebral hemorrhage, transient ischemic attack, and stroke mimics
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Positive predictive value (PPV) of existing and newly developed electroencephalography (EEG) algorithms based on ambulant EEG for detection of an large vessel occlusion of the posterior circulation (LVO-p), intracerebral hemorrhage, transient ischemic attack, and stroke mimics.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
NPV of existing and newly developed EEG algorithms for detection of LVO-p, intracerebral hemorrhage, transient ischemic attack, and stroke mimics
Délai: EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Negative predictive value (NPV) of existing and newly developed electroencephalography (EEG) algorithms based on ambulant EEG for detection of an large vessel occlusion of the posterior circulation (LVO-p), intracerebral hemorrhage, transient ischemic attack, and stroke mimics.
EEG-data for development of the algorithm will be recorded within 24 hours after onset of symptoms or last seen well
Technical feasibility of performing ambulant EEGs in the prehospital setting
Délai: Feedback on technical issues by the paramedic that performs the EEG and by the EEG-expert, will be collected directly at arrival in the emergency department (within 24 hours after the patient is included in the study)
Assessing whether it is technically possible for paramedics to perform ambulant electroencephalography (EEG) in patients with a suspected AIS in the prehospital setting.
Feedback on technical issues by the paramedic that performs the EEG and by the EEG-expert, will be collected directly at arrival in the emergency department (within 24 hours after the patient is included in the study)
Logistical feasibility of performing ambulant EEGs in the prehospital setting
Délai: Feedback on logistical issues by the paramedic that performs the EEG, will be collected directly at arrival in the emergency department (within 24 hours after the patient is included in the study)
Assessing whether it is logistically possible for paramedics to perform ambulant electroencephalography (EEG) in patients with a suspected AIS in the prehospital setting.
Feedback on logistical issues by the paramedic that performs the EEG, will be collected directly at arrival in the emergency department (within 24 hours after the patient is included in the study)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Les enquêteurs

  • Chercheur principal: Jonathan M Coutinho, MD, PhD, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

19 juin 2022

Achèvement primaire (Anticipé)

1 juin 2026

Achèvement de l'étude (Anticipé)

1 juin 2026

Dates d'inscription aux études

Première soumission

7 juin 2022

Première soumission répondant aux critères de contrôle qualité

27 juin 2022

Première publication (Réel)

29 juin 2022

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

29 juin 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

27 juin 2022

Dernière vérification

1 juin 2022

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • NL75429.018.20

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

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Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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