A Standard Carbon Dioxide Flushing Protocol to Reduce Air Embolization During Thoracic Endovascular Aortic Repair (FlushTEVAR)
FlushTEVAR is a non-profit, interventional, randomized, controlled, single-blind, national multicenter study promoted by the University of Bologna and coordinated by the Vascular Surgery Unit of IRCCS Azienda Ospedaliero-Universitaria di Bologna, Policlinico di Sant'Orsola, under the direction of Prof. Mauro Gargiulo, who also serves as Principal Investigator. The study aims to develop and evaluate a pre-implant thoracic endograft flushing technique using carbon dioxide (CO₂) to reduce periprocedural embolic events and cerebral infarctions in patients undergoing Thoracic Endovascular Aortic Repair (TEVAR).
TEVAR is currently the treatment of choice for acute aortic syndromes and aneurysms involving the descending thoracic aorta. Despite its widespread use, TEVAR remains associated with significant neurological complications, with an incidence ranging from 3% to 8% in standard procedures and reaching up to 16% in more complex endovascular interventions. Cerebral embolization caused by solid and gaseous particles is considered the main cause of perioperative stroke and silent brain infarction (SBI), the latter being defined as ischemic brain injury detected by neuroradiological imaging in the absence of immediate clinical symptoms. During TEVAR, approximately 90% of microembolic signals detected in the middle cerebral artery are caused by gaseous emboli, with the highest number occurring during endograft deployment. This phenomenon is associated with the manufacturing and sterilization processes of endografts, during which gas microparticles become trapped between the endograft and its delivery system and are subsequently released into the bloodstream when the device is deployed at the intended aortic site.
The primary objective of the study is to assess the difference in the incidence of major neurological events, including stroke and transient ischemic attack (TIA), as well as silent brain infarctions, between patients whose endografts undergo a standardized pre-implant flushing protocol with CO₂ followed by conventional saline flushing, and patients receiving standard saline flushing alone. Major neurological events will be assessed clinically, while silent brain infarctions will be evaluated using study-specific diffusion-weighted magnetic resonance imaging (DW-MRI) of the brain performed within 72 hours after the procedure.
A total of 90 patients will be enrolled across four participating centers and randomized in a 1:1 ratio after providing informed consent. Forty-five patients will be allocated to the experimental arm and treated with CO₂ flushing before the standard saline flushing procedure during TEVAR, while forty-five patients will be allocated to the control arm and will receive standard saline flushing only.
Eligible patients must be at least 18 years of age and present with type B acute aortic syndrome in the acute, subacute, or chronic phase, or thoracic and thoracoabdominal aneurysms with Crawford extent I, II, III, or IV. Written informed consent is required for participation. Patients will be excluded if the procedure is performed using CO₂ angiography, if endografts without a sheath are used, if emergency endovascular treatment is required, if they have experienced a stroke or TIA within the previous six months, if the proximal sealing zone is 0 or 1, if any contraindication to DW-MRI is present, or in cases of pregnancy or breastfeeding.
At study completion, the two treatment groups will be compared on the basis of diffusion-weighted brain MRI findings. The primary endpoint is the number of silent brain infarctions and the determination of whether a statistically significant difference exists between the CO₂ flushing group and the saline flushing group. The safety of the procedure will be evaluated through both technical and clinical success. The planned study duration is three years, and postoperative rates of SBI and TIA/stroke will be compared between groups using Fisher's and Pearson's chi-square tests.
Descripción general del estudio
Estado
Condiciones
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Mauro Gargiulo, MD
- Número de teléfono: +39 0512144252
- Correo electrónico: mauro.gargiulo2@unibo.it
Copia de seguridad de contactos de estudio
- Nombre: Chiara Mascoli, MD
- Número de teléfono: +39 0512144278
- Correo electrónico: chiara.mascoli@aosp.bo.it
Ubicaciones de estudio
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Italy
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Bologna, Italy, Italia, 40138
- Reclutamiento
- IRCCS Azienda Ospedaliero-Universitaria di Bologna
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Investigador principal:
- Mauro Gargiulo, MD
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Contacto:
- Mauro Gargiulo, MD
- Número de teléfono: +39 0512144252
- Correo electrónico: mauro.gargiulo2@unibo.it
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Contacto:
- Mascoli Chiara, MD
- Número de teléfono: +39 0512144278
- Correo electrónico: chiara.mascoli@aosp.bo.it
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Sub-Investigador:
- Chiara Mascoli, MD
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Sub-Investigador:
- Stefania Caputo, MD
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Brescia, Italy, Italia, 25123
- Aún no reclutando
- A.S.S.T. Spedali Civili di Brescia
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Contacto:
- Stefano Bonardelli, MD
- Número de teléfono: +39 3332929425
- Correo electrónico: stefano.bonardelli@unibs.it
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Investigador principal:
- Stefano Bonardelli, MD
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Genova, Italy, Italia, 16132
- Aún no reclutando
- IRCCS Policlinico San Martino di Genova
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Investigador principal:
- Giovanni Pratesi, MD
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Contacto:
- Giovanni Pratesi, MD
- Correo electrónico: Giovanni.Pratesi@unige.it
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Padova, Italy, Italia, 35128
- Aún no reclutando
- Azienda Ospedaliero-Universitaria di Padova
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Contacto:
- Franco Grego, MD
- Número de teléfono: +39 0498212638
- Correo electrónico: franco.grego@unipd.it
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Investigador principal:
- Franco Grego, MD
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age is at least 18 years
- Present with type B acute aortic syndrome in the acute, subacute, or chronic phase
- Thoracic and thoracoabdominal aneurysms with Crawford extent I, II, III, or IV
- Written informed consent
Exclusion Criteria:
- Procedure performed using CO₂ angiography
- Endografts without a sheath is used
- Emergency endovascular treatment required
- Patient has experienced a stroke or TIA within the previous six months
- Proximal sealing zone is 0 or 1
- Any contraindication to DW-MRI
- Pregnancy or breastfeeding
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: CO₂ flushing before the standard saline flushing procedure during TEVAR
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The CO2 flushing technique is conducted using an automated injector with the application of standard injection volume and pressure.
Specifically, the endoprosthesis will be flushed from the side port of the delivery system with 3 CO2 injections at 750 mmHg of pressure and 100 cc of volume.
Following the IFU, the endograft delivery system will be flushed with 60 ml of saline solution at 0.9%.
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Comparador activo: only standard saline flushing procedure during TEVAR
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Following the IFU, the endograft delivery system will be flushed with 60 ml of saline solution at 0.9%.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Assess the number and location of SBI using study-specific diffusion-weighted magnetic resonance imaging (DW-MRI) and determine if there is a statistically significant difference of SBI number in the "CO2 arm", compared to the "saline solution arm".
Periodo de tiempo: Up to 72 hours after endovascular repair
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The primary objective of the study is to assess the difference in terms of incidence (number) of ischaemic cerebral lesions, detected by DW-MRI after TEVAR, between patients whose endografts undergo a standardized pre-implant flushing protocol with CO₂ followed by conventional saline flushing, and patients receiving standard saline flushing alone,
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Up to 72 hours after endovascular repair
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Technical and clinical success
Periodo de tiempo: Peri-operatively
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Technical success: successfull endograft deployment, patency, absence of type I-III endoleak, retrograde dissections. Clinical success: absence of major stroke, death, paraplegia, major bleeding, acute kidney injury. |
Peri-operatively
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Mauro Gargiulo, MD, University of Bologna
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
- Trastornos cerebrovasculares
- Enfermedades Cerebrales
- Enfermedades del Sistema Nervioso Central
- Enfermedades del Sistema Nervioso
- Enfermedades Vasculares
- Enfermedades cardiovasculares
- Manifestaciones de la piel
- Isquemia cerebral
- Condiciones Patológicas, Signos y Síntomas
- Signos y síntomas
- Carrera
- Ataque Isquémico, Transitorio
- Aneurisma
- Enrojecimiento
Otros números de identificación del estudio
- FlushTEVAR
- Funding for a non-profit trial (Otro número de subvención/financiamiento: Angiodroid S.P.A.)
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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