首页> 外文OA文献 >Solitaire™ with the Intention for Thrombectomy as Primary Endovascular Treatment for Acute Ischemic Stroke (SWIFT PRIME) trial: protocol for a randomized, controlled, multicenter study comparing the Solitaire revascularization device with IV tPA with IV tPA alone in acute ischemic stroke.
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Solitaire™ with the Intention for Thrombectomy as Primary Endovascular Treatment for Acute Ischemic Stroke (SWIFT PRIME) trial: protocol for a randomized, controlled, multicenter study comparing the Solitaire revascularization device with IV tPA with IV tPA alone in acute ischemic stroke.

机译:Solitaire™旨在进行血栓切除术作为急性缺血性卒中的主要血管内治疗(SWIFT PRIME)试验:一项针对随机,对照,多中心研究的方案,比较了在急性缺血性卒中中Soltaire血运重建设备与IV tPA和单独的IV tPA进行比较。

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摘要

RATIONALEududEarly reperfusion in patients experiencing acute ischemic stroke is critical, especially for patients with large vessel occlusion who have poor prognosis without revascularization. Solitaire™ stent retriever devices have been shown to immediately restore vascular perfusion safely, rapidly, and effectively in acute ischemic stroke patients with large vessel occlusions.ududAIMududThe aim of the study was to demonstrate that, among patients with large vessel, anterior circulation occlusion who have received intravenous tissue plasminogen activator, treatment with Solitaire revascularization devices reduces degree of disability 3 months post stroke.ududDESIGNududThe study is a global multicenter, two-arm, prospective, randomized, open, blinded end-point trial comparing functional outcomes in acute ischemic stroke patients who are treated with either intravenous tissue plasminogen activator alone or intravenous tissue plasminogen activator in combination with the Solitaire device. Up to 833 patients will be enrolled.ududPROCEDURESududPatients who have received intravenous tissue plasminogen activator are randomized to either continue with intravenous tissue plasminogen activator alone or additionally proceed to neurothrombectomy using the Solitaire device within six-hours of symptom onset.ududSTUDY OUTCOMESududThe primary end-point is 90-day global disability, assessed with the modified Rankin Scale (mRS). Secondary outcomes include mortality at 90 days, functional independence (mRS ≤ 2) at 90 days, change in National Institutes of Health Stroke Scale at 27 h, reperfusion at 27 h, and thrombolysis in cerebral infarction 2b/3 flow at the end of the procedure.ududANALYSISududStatistical analysis will be conducted using simultaneous success criteria on the overall distribution of modified Rankin Scale (Rankin shift) and proportions of subjects achieving functional independence (mRS 0-2).
机译:急性缺血性卒中患者的早期再灌注至关重要,特别是对于大血管闭塞且预后较差而无血运重建的患者。研究表明,Solitaire™支架收回装置可在具有大血管闭塞的急性缺血性中风患者中立即安全,快速且有效地恢复血管灌注。 ud udAIM ud ud该研究的目的是证明,在大血管闭塞患者中血管,已接受静脉内纤溶酶原激活剂的前循环闭塞,使用纸牌血运重建设备治疗可降低卒中后3个月的残疾程度。 ud udDESIGN ud ud这项研究是一项全球性多中心,两臂,前瞻性,随机,开放性研究一项盲目的终点试验,比较了急性缺血性卒中患者的功能结局,这些患者单独接受静脉内组织纤溶酶原激活物或静脉内组织纤溶酶原激活物与纸牌设备联合治疗。最多将招募833名患者。 ud ud过程 ud ud接受静脉内组织纤溶酶原激活剂的患者被随机分配为继续单独使用静脉内纤溶酶原激活剂,或者在出现症状的六小时内使用Solitaire装置进行神经血栓切除术。 ud ud研究结果 ud ud主要终点是90天的全球残疾,使用改良的Rankin量表(mRS)进行评估。次要结局包括90天时的死亡率,90天时的功能独立性(mRS≤2),美国国立卫生研究院卒中量表的变化(27 h),27 h的再灌注以及脑梗死末期2b / 3血栓的血栓溶解。 ud udANALYSIS ud ud统计信息将使用同步成功标准对改良的Rankin量表的总体分布(Rankin移位)和实现功能独立性的受试者比例(mRS 0-2)进行统计分析。

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