NCT04618718已完成不适用
Cerebral Protection in Transcatheter Aortic Valve Replacement - The PROTEMBO C Trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 64
- 试验地点
- 14
- 主要终点
- Rate of Participants With MACCE Events
研究概览
简要总结
The PROTEMBO C Trial is an international, multi-center, single arm, non-inferiority study of the safety and performance of using the ProtEmbo System for cerebral embolic protection in subjects with severe native aortic valve stenosis indicated for TAVR.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •The heart team recommends transcatheter valve aortic valve replace consistent with the 2017 ESC/EACTS Guidelines for the management of valvular heart disease.
- •Compatible left subclavian artery (≥ 4 mm diameter) without significant stenosis (> 70%) and distance between the origin of left subclavian artery and valve plain of ≥ 90mm as determined by Multi-Slice Computed Tomography (MSCT) scan or equivalent imaging modality.
- •The subject and the treating physician agree that the subject will undergo the scheduled pre-procedural testing and return for all required post-procedure follow-up visits.
- •The subject is able to provide informed consent, has been informed of the nature of the trial, agrees to its provisions and has provided written informed consent as approved by the relevant regulatory authority of the respective clinical site.
- •Subject is a minimum of 18 years of age.
排除标准
- •Left upper limb vasculature in the left extremity precluding 6Fr sheath radial / brachial / subclavian access.
- •Inadequate circulation to the left extremity as evidenced by signs of artery occlusion (modified Allen's test) or absence of radial/brachial pulse.
- •Hemodialysis shunt, graft, or arterio-venous fistula involving the upper extremity vasculature.
- •TAVR conducted via other than transfemoral access (subclavian, axillar, transapical, transaortic, carotid or transcaval).
- •Evidence of an acute myocardial infarction ≤ 1 month before the intended treatment.
- •Aortic valve is a congenital unicuspid or bicuspid valve.
- •Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation >3+).
- •Any therapeutic invasive cardiac procedure resulting in a permanent implant that is performed within 30 days of the index procedure (unless part of planned strategy for treatment of concomitant coronary artery disease).
- •Blood dyscrasias as defined: Leukopenia, acute anemia, thrombocytopenia, history of bleeding diathesis or coagulopathy.
- •Hemodynamic instability requiring inotropic support or mechanical heart assistance.
- •Need for emergency surgery for any reason.
- •Severe hypertrophic cardiomyopathy with or without obstruction.
- •Severe ventricular dysfunction with LVEF ≤30%.
- •Echocardiographic evidence of intracardiac or aortic mass, thrombus, or vegetation.
- •Symptomatic or asymptomatic severe (≥ 70%) occlusive carotid disease requiring concomitant CEA / stenting.
- •Subject has undergone carotid stenting or carotid endarterectomy within the previous 6 weeks.
- •Active peptic ulcer or upper GI bleeding within the prior 6 months.
- •A known hypersensitivity or contraindication to aspirin, heparin, ticlopidine, or clopidogrel, device component material, or sensitivity to contrast media, which cannot be adequately premedicated.
- •Recent (within 6 months) CVA or a TIA.
- •Renal insufficiency (creatinine > 3.0 mg / dL or GFR < 30) and / or renal replacement therapy at the time of screening.
- •Life expectancy < 12 months due to non-cardiac co-morbid conditions.
- •Subjects in whom anti-platelet and / or anticoagulant therapy is contraindicated, or who will refuse transfusion.
- •Subjects who have active bacterial endocarditis or other active infections.
- •Currently participating in an investigational drug or another device study.
- •Subjects who have a planned treatment with any other investigational device or procedure during the study follow-up period (30 days).
- •Subjects with planned concomitant surgical or transcatheter ablation for Atrial Fibrillation during the study follow-up period (30 days).
- •Any subject with a balloon valvuloplasty (BAV) within 30 days of the procedure.
- •Subject is a woman of child-bearing potential.
- •Patient with Heparin-Induced Thrombocytopenia Syndrome.
- •Inner diameter of aortic arch is less than 25mm.
- •Brachiocephalic trunk originating from the aortic arch that splits into the bilateral subclavian arteries and a bicarotid trunk (Origin D).
- •Hepatic failure (defined as liver enzyme elevations two times the upper limit of normal) or active infectious hepatitis
- •Cardiogenic shock or severe hypotension (systolic blood pressure < 90 mm Hg) at the time of the index procedure
- •Subjects who have a planned concomitant cardiac surgical or interventional procedure (e.g., coronary revascularization) during the TAVI procedure
- •Subjects who have a pre-existing prosthetic heart valve in any position
- •Neurological:
- •Subject had active major psychiatric disease.
- •Subject has severe visual, auditory, or learning impairment and is unable to comprehend English or local language and therefore unable to be consented for the study.
- •Subjects with neurodegenerative or other progressive neurological disease or history of significant head trauma followed by persistent neurologic defaults or known structural brain abnormalities.
- •Angiographic:
- •Excessive tortuosity or severe peripheral arterial disease in the left radial / brachial / subclavian artery preventing ProtEmbo System access and insertion.
- •Subject whose left radial / brachial / subclavian artery reveals significant stenosis, calcification, ectasia, dissection, occlusion or aneurysm, in particular at or within 3 cm of the aortic ostium.
- •Subject with significant stenosis, ectasia, dissection, or aneurysm in the ascending aorta or in the aortic arch, or with abnormal aortic arch angulation or abnormal anatomical conditions of the aorta.
- •Magnetic Resonance Imaging:
- •Subject Body Mass Index (BMI) precluding imaging in scanner.
- •Contraindications to MRI (subjects with any implantable temporary or permanent pacemaker or defibrillator, metal implants in field of view, metallic fragments, clips, or devices in the brain or eye before TAVR procedure).
- •Subjects who have a high risk of complete AV block after TAVR, with the need of permanent pacemaker (e.g. subjects with preexisting bifascicular block or complete right bundle branch block plus any degree of AV block).
- •Planned implantation of a pacemaker or defibrillator implantation within the first 4 days after TAVR.
- •Claustrophobia precluding MRI scanning.
- •No scanner hardware, software, coil or protocol changes during the course of the study.
结局指标
主要结局
Rate of Participants With MACCE Events
时间窗: 30 days post-procedure
Number of participants experiencing a Major Adverse Cardiac and Cerebrovascular Event (MACCE) defined by VARC-2 including all-cause mortality, all stroke, life-threatening or disabling bleeding, vascular injury and acute kidney injury (stage 2 or 3) within 30 days of the procedure
Rate of Participants in Whom Technical Success Was Achieved
时间窗: During the procedure
Number of participants in whom technical success was achieved during the procedure. Technical success is defined as the ability to safely deliver, deploy, and remove the device, ability to secure positioning and stability of the position throughout the transcatheter intracardiac procedure and ability to deflect embolic material as assessed by adequate coverage while not impeding blood flow, deployed and removed and positioning and stability of the device
次要结局
- Efficacy-MR Imaging: Comparison Between the Median New Lesion Volume in the Brain(2-7 days post-procedure)
- Composite Rate of Death or All Strokes(3 days post-procedure)
研究者
研究点 (14)
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