Combined Selective Endovascular Brain Hypothermia with Edaravone Dexborneol versus Edaravone Dexborneol Alone for Endovascular Treatment in Acute Ischemic Stroke (SHE): Protocol for a Multicenter, Single-Blind, Randomized Controlled Study.

IF 2.2 3区 医学 Q3 CLINICAL NEUROLOGY
Xin Jiang, Lizhang Chen, Jian Wang, Jinghuan Fang, Mengmeng Ma, Muke Zhou, Hongbo Zheng, Fayun Hu, Dong Zhou, Li He
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引用次数: 0

Abstract

Introduction: Selective endovascular brain hypothermia has been proposed as a potential neuroprotective strategy; however, its effectiveness is still not well established. The primary objective of this trial is to investigate the efficacy and safety of selective endovascular brain hypothermia with edaravone dexborneol for endovascular treatment in acute ischemic stroke (AIS).

Methods: The SHE study is a multicenter, single-blind, randomized controlled clinical trial. Patients with acute anterior circulation ischemic stroke who received endovascular treatment within 24 h after stroke onset and achieved successful recanalization will be enrolled and centrally randomized into combined selective endovascular brain hypothermia with edaravone dexborneol or edaravone dexborneol alone groups in a 1:1 ratio (n = 564). Patients allocated to the hypothermia group will receive 300 mL cool saline at 4°C through guiding catheter (30 mL/min) into target vessel within 3 min after recanalization and then receive edaravone dexborneol (edaravone dexborneol 15 mL + NS 100 mL ivgtt bid for 10-14 days) within 24 h after admission. The control group will receive 300 mL 37°C saline (30 mL/min) infused into target vessel through guiding catheter and then receive edaravone dexborneol. All patients enrolled will receive standard care according to current guidelines for stroke management. The primary outcome is the proportion of functional independence, defined as a mRS score of 0-2 at 90 days after randomization.

Conclusion: This is a randomized clinical trial with a large sample size to compare combined selective endovascular brain hypothermia and edaravone dexborneol with edaravone dexborneol alone in patients with acute anterior ischemic stroke. The SHE trial aims to provide further evidence of the benefit of selective endovascular brain hypothermia in AIS patients who received endovascular treatment.

急性缺血性脑卒中血管内治疗联合选择性脑血管内低温治疗与单用依达拉奉-地塞米松相比(SHE):多中心、单盲、随机对照研究方案》。
引言 选择性血管内脑部低温疗法作为一种潜在的神经保护策略已被提出,但其有效性尚未得到充分证实。本试验的主要目的是研究在急性缺血性卒中(AIS)的血管内治疗中使用依达拉奉-地塞米松选择性血管内脑部低温的有效性和安全性。方法 SHE 研究是一项多中心、单盲、随机对照临床试验。急性前循环缺血性卒中患者在卒中发生后 24 小时内接受血管内治疗并成功实现再通后,将被纳入该研究,并按 1:1 的比例集中随机分配到联合选择性血管内脑部低温治疗与依达拉奉-右旋波旁醇组或单独依达拉奉-右旋波旁醇组(n=564)。低温组患者将在再通血管后 3 分钟内通过导引导管(30 毫升/分钟)向靶血管输入 300 毫升 4℃ 低温生理盐水,然后在入院后 24 小时内接受依达拉奉-右旋波旁醇治疗(依达拉奉-右旋波旁醇 15 毫升 +NS 100 毫升 ivgtt bid,10 至 14 天)。对照组将通过导引导管向靶血管注入 300 毫升 37℃的生理盐水(30 毫升/分钟),然后接受依达拉奉-右旋波旁醇治疗。所有入组患者都将按照现行中风治疗指南接受标准治疗。主要结果是功能独立的比例,即随机分组后 90 天的 mRS 评分为 0-2 分。结论 这是一项样本量较大的随机临床试验,旨在对急性前部缺血性脑卒中患者联合选择性脑血管内低温疗法和依达拉奉-右旋糖苷与单独依达拉奉-右旋糖苷进行比较。SHE 试验旨在进一步证明选择性血管内脑部低温疗法对接受血管内治疗的 AIS 患者的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cerebrovascular Diseases
Cerebrovascular Diseases 医学-临床神经学
CiteScore
4.50
自引率
0.00%
发文量
90
审稿时长
1 months
期刊介绍: A rapidly-growing field, stroke and cerebrovascular research is unique in that it involves a variety of specialties such as neurology, internal medicine, surgery, radiology, epidemiology, cardiology, hematology, psychology and rehabilitation. ''Cerebrovascular Diseases'' is an international forum which meets the growing need for sophisticated, up-to-date scientific information on clinical data, diagnostic testing, and therapeutic issues, dealing with all aspects of stroke and cerebrovascular diseases. It contains original contributions, reviews of selected topics and clinical investigative studies, recent meeting reports and work-in-progress as well as discussions on controversial issues. All aspects related to clinical advances are considered, while purely experimental work appears if directly relevant to clinical issues.
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