75 A prospective, multi-center, randomized controlled pivotal study to evaluate the safety and effectiveness of trufill® NBCA embolization of the middle meningeal artery for the treatment of subdural hematoma – The membrane study

C. Kellner, F. Al‐Mufti, Rajesh K. Gupta, B. Jankowitz, R. Starke, A. Rai
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Abstract

Introduction Chronic subdural hematoma (cSDH) is one of the most common neurosurgical diseases with an incidence of 1-5.3 cases per 100,000 that increases significantly with age. When symptomatic, these lesions are often treated by surgery, an approach which does not directly address the underlying pathophysiology of chronic inflammation and neovascularization of the dura and has a high incidence of recurrence. Middle meningeal artery (MMA) embolization has emerged as a potential minimally invasive endovascular treatment option that may substitute for surgery or serve as an adjunct. TRUFILL n-BCA is potentially well suited as a liquid embolic in this procedure given that it is non-caustic, rapidly deployed, and able to be injected in a highly targeted fashion. Here we present the protocol for a randomized clinical trial to evaluate the safety and effectiveness of n-BCA embolization of the MMA for the treatment of cSDH. Methods This investigational trial is a prospective, multi-center, open-label, randomized controlled study in which up to 376 subjects will be randomized to receive standard of care (SOC) alone or SOC and TRUFILL n-BCA MMA embolization for the treatment of cSDH. The study is designed to evaluate the effectiveness and safety of MMA in two cohorts - a surgical cohort and a non-surgical cohort. Results Study EndpointsThe primary study effectiveness endpoint is the incidence of residual or re-accumulation of the cSDH (>10 mm) at 6 months as assessed by an independent core laboratory OR re-operation or surgical procedure on the hematoma within 6 months post randomization. Secondary effectiveness endpoints include mean reduction of hematoma volume at 3, 6 and 12 months compared to baseline, reduction > 50% in hematoma volume at 3, 6 and 12 months as well as others. Secondary safety endpoints include death, stroke, myocardial infarction or thromboembolic complications within 3, 6 and 12 months as well as others. Secondary health economics endpoints include hospital days, intensive care unit days, and change in the EQ-5D-5L score at discharge and 6 months compared to baseline. Conclusion Middle meningeal artery embolization with n-BCA is an emerging treatment strategy for cSDH. An appropriately powered trial like the MEMBRANE Study will provide high level evidence on the potential safety and efficacy of this treatment paradigm. Disclosures C. Kellner: 1; C; Penumbra, Siemens, Cerebrotech, Viz.AI, Minnetronix. 4; C; Metis Innovative. F. Al-Mufti: None. R. Gupta: None. B. Jankowitz: None. R. Starke: None. A. Rai: None.
一项前瞻性、多中心、随机对照的关键研究,旨在评估trufill®NBCA栓塞脑膜中动脉治疗硬膜下血肿的安全性和有效性
慢性硬膜下血肿(cSDH)是最常见的神经外科疾病之一,发病率为每100,000例1-5.3例,随着年龄的增长而显著增加。当有症状时,这些病变通常通过手术治疗,这种方法不能直接解决慢性炎症和硬脑膜新生血管的潜在病理生理,并且复发率很高。脑膜中动脉(MMA)栓塞已经成为一种潜在的微创血管内治疗选择,可以替代手术或作为辅助手段。TRUFILL n-BCA是非腐蚀性的、快速部署的,并且能够以高度靶向的方式注射,因此可能非常适合作为液体栓塞剂。在这里,我们提出了一项随机临床试验的方案,以评估n-BCA栓塞MMA治疗cSDH的安全性和有效性。该研究是一项前瞻性、多中心、开放标签、随机对照研究,其中多达376名受试者将随机接受单独的标准治疗(SOC)或SOC和TRUFILL n-BCA MMA栓塞治疗cSDH。该研究旨在评估MMA在两个队列中的有效性和安全性-一个手术队列和一个非手术队列。研究的主要有效性终点是6个月时cSDH残留或再积累(>10 mm)的发生率,由独立的核心实验室评估,或随机分组后6个月内血肿的再手术或外科手术。次要有效性终点包括与基线相比,3、6和12个月时血肿体积平均减少,3、6和12个月时血肿体积减少> 50%,以及其他。次要安全终点包括3个月、6个月和12个月内的死亡、中风、心肌梗死或血栓栓塞性并发症等。二级卫生经济学终点包括住院天数、重症监护病房天数以及出院时和6个月时EQ-5D-5L评分与基线相比的变化。结论n-BCA栓塞脑膜中动脉是一种新兴的治疗cSDH的方法。像膜研究这样的适当的试验将为这种治疗模式的潜在安全性和有效性提供高水平的证据。C. Kellner: 1;C;4 . Penumbra, Siemens, Cerebrotech, Viz.AI, minneapolis;C;美逖斯创新。F. Al-Mufti:没有。古普塔:没有。B. Jankowitz:没有。R.斯塔克:没有。A.雷:没有。
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