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The ASSURE ROT Registry: Bioresorbable Vascular Scaffold Following Rotablation for Complex Coronary Lesions (ASSURE ROT)

5 de febrero de 2015 actualizado por: Medical Care Center Prof. Mathey, Prof. Schofer, Ltd.

Postmarketing Surveillance Registry to Monitor Everolimus-eluting Bioresorbable Vascular Scaffold Following Rotational Atherectomy for the Treatment of Complex Coronary Lesions - The ASSURE ROT Registry

The registry aims to evaluate the safety, performance and efficacy of the Everolimus-eluting bioresorbable vascular scaffold (BVS) system following rotational atherectomy in patients with complex de novo native coronary artery lesions in all-day clinical practice.

Descripción general del estudio

Descripción detallada

Bioresorbable scaffolds are transient implants. They act like drug-eluting metallic stents (DES) during the first 3 months by supporting the vessel wall thereby keeping the artery patent. Subsequently, resorption of the scaffold begins and its structure loosens. As a result of everolimus release, neointimal growth is inhibited similar to DES. Finally the implant is reabsorbed completely in about 2-3 years. BVS in terms of late stent thrombosis may be safer than DES. Transiently scaffolded vessels may regain their natural curvature and angulation as well as response to nitroglycerine and endothelial function.

Tipo de estudio

De observación

Inscripción (Anticipado)

42

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Detlef G Mathey, Prof. Dr.
  • Número de teléfono: 152 +4940889009
  • Correo electrónico: dgmathey@web.de

Ubicaciones de estudio

      • Hamburg, Alemania, 22391
        • Reclutamiento
        • Medical Care Center Prof. Mathey, Prof. Schofer GmbH
        • Contacto:
          • Detlef G Mathey, Prof. Dr.
          • Número de teléfono: 152 +4940889009
          • Correo electrónico: dgmathey@web.de
        • Sub-Investigador:
          • Joachim Schofer, Prof. Dr.
        • Sub-Investigador:
          • Carsten Schwencke, PD Dr.

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 75 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra de probabilidad

Población de estudio

Patients with complex coronary artery lesions

Descripción

The recommendation to implant BVS in an individual patient in whom rotational atherectomy of a complex target lesion has been conducted, is purely based on clinical grounds. These are determined by the instructions for use (IFU) of the BVS and by the clinical experience accumulated so far from clinical studies.These studies suggest that the BVS should be implanted under certain conditions, which are determined by the patient and the coronary lesion treated:

Eligible:

Regarding to patient

  • Patient ≥ 18 and ≤ 75 years with a live expectancy of at least 5 years with ischemic heart disease (chronic, NSTEMI and unstable angina) due to one or more complex de novo native coronary artery lesions
  • Patients with evidence of myocardial ischemia

Regarding to lesion

  • Reference vessel diameter ≥ 2.5 mm and ≤ 3.8 mm, visually estimated or by online QCA
  • Percent diameter stenosis ≥ 50% and < 100%, visually estimated or by online QCA
  • TIMI ≥1
  • Previous interventions of target vessel lesions should have been done ≥ 6 months prior to index procedure and > 10 mm distal to the target lesion
  • Previous interventions of non-target vessel lesions should have been done ≥ 30 days prior to index procedure

Not eligible:

Regarding to patient

  • Patient in whom antiplatelet therapy and/or anticoagulant therapy is contraindicated
  • Patient with a known hypersensitivity or contraindication to aspirin, both heparin and bivalirudin, clopidogrel, ticlopidine, prasugrel and ticagrelor, everolimus, poly (L-lactide), poly (D,L-lactide), or platinum, or with contrast sensitivity, who cannot be adequately premedicated
  • Patient has a known diagnosis of acute myocardial infarction (STEMI) within 72 hours preceding the index procedure and CK and CK-MB have not returned within normal limits at the time of procedure
  • Patient is currently experiencing clinical symptoms consistent with STEMI
  • Patient has current unstable arrhythmias
  • Patient has a known left ventricular ejection fraction < 30%
  • Patient has received a heart transplant or any other organ transplant or is waiting for any organ transplant
  • Patient receiving or scheduled to receive chemotherapy for malignancy within 30 days prior to or after procedure
  • Patient is receiving immunosuppression therapy and has known immunosuppressive or autoimmune disease
  • Patient is receiving or scheduled to receive chronic anticoagulation therapy
  • Elective surgery is planned within the first 6 month after the procedure that will require discontinuing either aspirin or clopidogrel
  • Patient has a platelet count < 100 000 cells/mm3 or > 700 000 cells/mm3, a WBC of
  • < 3000 cells/mm3, or documented or suspected liver disease
  • Patient has known renal insufficiency
  • Patient has a history of bleeding diathesis or coagulopathy or will refuse blood transfusions
  • Patient has cerebrovascular accident or transient ischemic neurological attack within the past six month
  • Patient has had a significant GI or urinary bleed within the past six months
  • Patient has extensive peripheral vascular disease that precludes safe 6 French sheath insertion
  • Patient has other medical illness (e.g., cancer or congestive heart failure) or known history of substance abuse (alcohol, cocaine, heroin etc.) that may cause noncompliance with the clinical study plan, confound the data interpretation or is associated with a limited life expectancy (i.e., les than one year)
  • Women of childbearing potential who have not undergone surgical sterilization or are not post- menopausal

Regarding to lesion

Target lesion(s) meets none of the following criteria:

  • Aorto-ostial location
  • Left main location
  • Located within 2 mm of the origin of LAD or LCX
  • Located within an arterial or saphenous vein graft or distal to a diseased (defined as vessel irregularity per angiogram and > 20% stenosed lesion by visual estimation) arterial or saphenous vein graft
  • Ostial lesion > 40% stenosed by visual estimation or side branch requiring predilation
  • Excessive tortuosity proximal to or within the lesion (extreme angulation proximal to or within the lesion)
  • Restenotic from previous intervention

Target vessel is not containing thrombus

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Modelos observacionales: Grupo
  • Perspectivas temporales: Futuro

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Major Adverse Cardiac Event (MACE)
Periodo de tiempo: at 24 months
Composite of ischemia driven target lesion revascularisation (TLR), myocardial infarction and cardiac death
at 24 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Acute procedural success
Periodo de tiempo: At the end of hospital stay (maximum of 7 days)
Achievement of final in-scaffold residual stenosis of < 50% and TIMI flow 3 of the target site. Successful delivery and deployment of at least one study scaffold at the intended target lesion and successful withdrawal of the delivery system for all target lesions without occurrence of cardiac death, target vessel MI or repeat TLR during hospital stay (maximum of 7 days). In dual target lesion setting both lesions must meet clinical procedure success criteria.
At the end of hospital stay (maximum of 7 days)
Acute device success
Periodo de tiempo: At time of intervention
Successful delivery and deployment of the first scaffold at the intended target lesion (in overlapping setting both planned scaffolds) and successful withdrawal of delivery system. Attainment of < 50 % residual stenosis and TIMI flow 3 of the target site, using the BVS without the need for other non- study stents.
At time of intervention
Scaffold thrombosis
Periodo de tiempo: At time of intervention, and at 6, 12, 24, and 36 months
At time of intervention, and at 6, 12, 24, and 36 months
Cardiac death
Periodo de tiempo: At time of intervention, and at 6, 12,24, and 36 months
At time of intervention, and at 6, 12,24, and 36 months
Myocardial infarction
Periodo de tiempo: At time of intervention, and at 6, 12, 24, and 36 months
At time of intervention, and at 6, 12, 24, and 36 months
Ischemia driven target lesion revascularisation (TLR)
Periodo de tiempo: At time of intervention, participants will be followed for the duration of hospital stay (an expected average of 3 days), at 6, 12, 24, and 36 months
Composite of ischemia driven target lesion revascularisation (TLR), myocardial infarction and cardial death
At time of intervention, participants will be followed for the duration of hospital stay (an expected average of 3 days), at 6, 12, 24, and 36 months
Ischemia driven target vessel revascularisation (TVR)
Periodo de tiempo: at 6, 12, 24, and 36 month
at 6, 12, 24, and 36 month
In-lesion % diameter stenosis
Periodo de tiempo: Baseline and final at time of intervention and at 24 months FU
QCA: Independent CoreLab
Baseline and final at time of intervention and at 24 months FU
Minimal lumen diameter (MLD)
Periodo de tiempo: Baseline and final at time of intervention and at 24 months FU
QCA: Independent CoreLab
Baseline and final at time of intervention and at 24 months FU
In-scaffold late lumen loss (LLL)
Periodo de tiempo: At 24 months FU
At 24 months FU

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Detlef G Mathey, Prof. Dr., Medical Care Center Prof. Mathey, Prof. Schofer GmbH

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de agosto de 2013

Finalización primaria (Anticipado)

1 de agosto de 2015

Finalización del estudio (Anticipado)

1 de agosto de 2017

Fechas de registro del estudio

Enviado por primera vez

29 de julio de 2013

Primero enviado que cumplió con los criterios de control de calidad

1 de agosto de 2013

Publicado por primera vez (Estimar)

2 de agosto de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

6 de febrero de 2015

Última actualización enviada que cumplió con los criterios de control de calidad

5 de febrero de 2015

Última verificación

1 de febrero de 2015

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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