Un estudio fundamental que evalúa la seguridad y la eficacia del catéter de punta adaptable en pacientes con accidente cerebrovascular isquémico agudo (PHAST)
Un Estudio Pivotal Prospectivo, Primero en Humanos, para Evaluar el Catéter de Punta Adaptativa Utilizado en el Tratamiento de Pacientes con Accidente Cerebrovascular Isquémico Agudo Durante la Trombectomía Mecánica
The purpose of this study is to assess the safety and the effectiveness of the Adaptive Tip Catheter (ATC) used as a first line direct aspiration thrombectomy technique for patients suffering of an acute ischemic stroke.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Adriana Popovici
- Número de teléfono: +41 76 396 34 66
- Correo electrónico: apopovi3@its.jnj.com
Copia de seguridad de contactos de estudio
- Nombre: Arnaud Nicolas, PhD
- Número de teléfono: +41 79 517 97 36
- Correo electrónico: anicolas@its.jnj.com
Ubicaciones de estudio
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Heidelberg, Alemania, 69120
- Reclutamiento
- Universitaetsklinikum Heidelberg
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Kiel, Alemania, 24105
- Reclutamiento
- Universitatsklinikum Schleswig Holstein Kiel
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Mainz, Alemania, 55101
- Reclutamiento
- Universitaetsmedizin Mainz
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Solingen, Alemania, 42653
- Reclutamiento
- Stadtisches Klinikum Solingen gemeinnutzige GmbH
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Edegem, Bélgica, 2650
- Reclutamiento
- UZ Antwerpen
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Ghent, Bélgica, 9000
- Reclutamiento
- Ghent University Hospital
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Leuven, Bélgica, 3000
- Reclutamiento
- Universitair Ziekenhuis Leuven
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Bordeaux, Francia, 33076
- Reclutamiento
- CHU Bordeaux
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Nantes, Francia, 44093
- Reclutamiento
- CHU Nantes
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Paris, Francia, 75013
- Reclutamiento
- CHU Pitie Salpetriere
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Toulouse, Francia, 31059
- Reclutamiento
- Centre Hospitalier Universitaire de Toulouse - Hopital Purpan
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Tours, Francia, 37000
- Reclutamiento
- CHRU de Tours
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Dublin, Irlanda, 00000
- Reclutamiento
- Beaumont Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion criteria:
- Age greater than or equal to (>=) 18 years, less than or equal to (<=) 90 years, at the time of consent
- Signs and symptoms consistent with the diagnosis of acute ischemic stroke in the anterior circulation that can be treated with endovascular thrombectomy approaches
- Endovascular treatment can be initiated (defined as access puncture) within 24 hours from time last known well
- Baseline National Institutes of Health Stroke Scale (NIHSS) score >= 6
- Baseline Alberta Stroke Program Early CT Score (ASPECTS) >= 3
- A signed and dated Informed Consent Form (ICF) or Investigator Statement for emergency procedure (as allowed according to country regulations and approved by EC) has been obtained
Exclusion criteria:
- Known pregnancy, as evidenced by positive pregnancy test for women of childbearing potential or breast feeding
- Life expectancy less than (<) 90 days prior to stroke onset
- Known hemorrhagic diathesis disorder, coagulation factor deficiency or oral anticoagulant therapy with known International Normalized Ratio (INR) greater than (>) 3.0
- Clinical symptoms and/or CT/MRI evidence suggestive of bilateral stroke or stroke in multiple vascular territories, defined as occlusions in more than one vessel not downstream from each other (for example, bilateral anterior circulation, anterior/posterior circulation)
- Clinical history, past imaging or clinical judgement suggest that the intracranial occlusion is chronic
- Computed Tomography/ Magnetic Resonance Imaging (CT/MRI) evidence of recent/fresh hemorrhage
- Baseline CT or MRI showing mass effect
- Currently participating in an investigational (drug, device, etc.) clinical trial that may confound study endpoints. Patients in observational, natural history, and/or epidemiological studies not involving intervention are eligible
- Cerebral catheter angiographic evidence of pre-existing arterial disease, that potentially impacts treatment and/or outcome (for example, vasculitis)
- Any occlusion or stenosis that limits device access to the target area (for example, carotid dissection, tandem occlusions) or requiring acute stenting to achieve access
- Cerebral catheter angiographic evidence of multiple cerebrovascular occlusions, defined as occlusions in more than one vessel not downstream from each other (for example, bilateral anterior circulation, anterior/posterior circulation)
- Excessive vascular access tortuosity that will likely prevent endovascular access with the adaptive tip catheter (ATC)
- Baseline expanded thrombolysis in cerebral infarction (eTICI) > 1
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Adaptive Tip Catheter (ATC)
The ATC will be used alone (direct aspiration) as the first attempted device/technique for mechanical thrombectomy in the anterior circulation in patients during the first three passes or until final reperfusion, if less than three passes are needed. Patients will be followed over 90 days post procedure. |
Patients will undergo mechanical thrombectomy using ATC. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Third Pass Reperfusion Assessed by Independent Imaging Core Lab
Periodo de tiempo: Intraoperative
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Successful achievement of the third pass reperfusion is defined as achieving an Expanded Thrombolysis in Cerebral Infarction (eTICI) score of 2b50 or greater using no more than three passes with the study device in the target vessel, and without any rescue therapy. |
Intraoperative
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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First Pass Reperfusion
Periodo de tiempo: Intraoperative
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Successful achievement of the first pass reperfusion is defined as achieving an eTICI score of 2c or greater, as determined by the independent imaging core lab, with one pass of the study device in the target vessel, and without any rescue therapy. |
Intraoperative
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Final Procedural Reperfusion
Periodo de tiempo: Intraoperative
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Successful achievement of the final procedural reperfusion is defined as achieving a final (end of procedure) eTICI score of 2b50 or greater in the target vessel as determined by the independent imaging core lab. |
Intraoperative
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Modified Rankin Scale (mRS) Score of 0-2 at 90 days Post-Procedure
Periodo de tiempo: At 90 days post-procedure
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Percentage of patients with mRS score of 0-2 at 90 days or no change from baseline if pre-ictal mRS greater than (>) 2 will be reported. |
At 90 days post-procedure
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Vessel Damage
Periodo de tiempo: At 90 days post-procedure
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Number of patients with perforation or dissection in the blood vessel known to be related to or possibly related to the study device will be reported. |
At 90 days post-procedure
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All-Cause Mortality
Periodo de tiempo: At 90 days post-procedure
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All mortality regardless of causes at 90 days post-procedure will be reported. |
At 90 days post-procedure
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Symptomatic Intracranial Hemorrhage (sICH) at 24 hours
Periodo de tiempo: At 24 hours after intervention
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sICH is defined as a new intracranial hemorrhage as detected by brain imaging, measured 24 hours after intervention associated with any of the following: greater than or equal to (>=) 4 points total National Institutes of Health Stroke Scale (NIHSS) at the time of diagnosis compared to immediately before worsening; >= 2 point in one NIHSS category; leading to intubation/hemicraniectomy/external ventricular drain (EVD) placement or other major medical/surgical intervention or absence of alternative explanation for deterioration. |
At 24 hours after intervention
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Christophe Cognard, MD-PhD, CHU Toulouse - Hôpital, Purpan, Toulouse France
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
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- CNV202304
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
The data sharing policy of Johnson & Johnson Innovative Medicine is available at www.innovativemedicine.jnj.com/our-innovation/clinical-trials/transparency. As noted on this site, requests for access to the study data can be submitted through Yale Open Data Access (YODA) Project site at yoda.yale.edu.
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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