Hong Ji Man, Choi Mun Hee, Sohn Sung-Il, Hwang Yang-Ha, Ahn Seong Hwan, Lee Yeong-Bae, Shin Dong-Ick, Chamorro Ángel, Choi Dennis W
Department of Neurology, Ajou University School of Medicine, Ajou University Medical Center, 164, World cup-ro, Yongtong-gu, Suwon-si, Kyunggi-do, 442-749, Republic of Korea.
Department of Neurology, Dongsan Medical Center, Keimyung University, Daegu, Republic of Korea.
Trials. 2018 Jul 13;19(1):375. doi: 10.1186/s13063-018-2746-9.
The potential of neuroprotective agents should be revisited in the era of endovascular thrombectomy (EVT) for acute large-artery occlusion because their preclinical effects have been optimized for ischemia and reperfusion injury. Neu2000, a derivative of sulfasalazine, is a multi-target neuroprotectant. It selectively blocks N-methyl-D-aspartate receptors and scavenges for free radicals. This trial aimed to determine whether neuroprotectant administration before EVT is safe and leads to a more favorable outcome.
This trial is a phase-II, multicenter, three-arm, randomized, double-blinded, placebo-controlled, blinded-endpoint drug trial that enrolled participants aged ≥ 19 years undergoing an EVT attempt less than 8 h from symptom onset, with baseline National Institutes of Health Stroke Scale (NIHSS) score ≥ 8, Alberta Stroke Program Early CT score ≥ 6, evidence of large-artery occlusion, and at least moderate collaterals on computed tomography angiography. EVT-attempted patients are randomized into control, low-dose (2.75 g), and high-dose (5.25 g) Neu2000KWL over 5 days. Seventy participants per group are enrolled for 90% power, assuming that the treatment group has a 28.4% higher proportion of participants with functional independence than the placebo group. The primary outcome, based on intention-to-treat criteria is the improvement of modified Rankin Scale (mRS) scores at 3 months using a dichotomized model. Safety outcomes include symptomatic intracranial hemorrhage within 5 days. Secondary outcomes are distributional change of mRS, mean differences in NIHSS score, proportion of NIHSS score 0-2, and Barthel Index > 90 at 1 and 4 weeks, and 3 months.
The trial results may provide information on new therapeutic options as multi-target neuroprotection might mitigate reperfusion injury in patients with acute ischemic stroke before EVT.
ClinicalTrials.gov, ID: NCT02831088 . Registered on 13 July 2016.
在急性大动脉闭塞的血管内血栓切除术(EVT)时代,神经保护剂的潜力值得重新审视,因为它们的临床前效果已针对缺血和再灌注损伤进行了优化。Neu2000是柳氮磺胺吡啶的衍生物,是一种多靶点神经保护剂。它能选择性阻断N-甲基-D-天冬氨酸受体并清除自由基。本试验旨在确定在EVT前给予神经保护剂是否安全,并能带来更有利的结果。
本试验是一项II期、多中心、三臂、随机、双盲、安慰剂对照、盲终点药物试验,纳入年龄≥19岁、在症状发作后8小时内接受EVT尝试、基线美国国立卫生研究院卒中量表(NIHSS)评分≥8、阿尔伯塔卒中项目早期CT评分≥6、有大动脉闭塞证据且计算机断层血管造影显示至少有中度侧支循环的参与者。尝试进行EVT的患者被随机分为对照组、低剂量(2.75 g)和高剂量(5.25 g)Neu2000KWL组,为期5天。每组招募70名参与者,以达到90%的检验效能,假设治疗组功能独立参与者的比例比安慰剂组高28.4%。基于意向性分析标准的主要结局是使用二分法模型在3个月时改良Rankin量表(mRS)评分的改善情况。安全性结局包括5天内出现症状性颅内出血。次要结局是mRS的分布变化、NIHSS评分的平均差异、NIHSS评分为0-2的比例以及在1周、4周和3个月时Barthel指数>90的情况。
试验结果可能会提供有关新治疗选择的信息,因为多靶点神经保护可能会减轻急性缺血性卒中患者在EVT前的再灌注损伤。
ClinicalTrials.gov,标识符:NCT02831088。于2016年7月13日注册。