阿托伐他汀治疗自发性蛛网膜下腔出血:随机双盲安慰剂对照试验的研究方案

Junhui Chen, Yu-hai Wang
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摘要

背景:动物研究已经证实他汀类药物在蛛网膜下腔出血期间和之后具有神经保护作用;然而,他汀类药物对人类的治疗效果仍然存在争议。他汀类药物治疗自发性蛛网膜下腔出血的临床应用数据目前的解释受限于研究中使用的小样本量,因此很难得出他汀类药物多重神经保护作用的有效结论。因此,我们建议开展随机双盲安慰剂对照平行组临床试验,以确定阿托伐他汀对自发性蛛网膜下腔出血、脑脊液中细胞凋亡相关因子、血清炎症因子的影响,并观察其缓解血管痉挛介导的神经保护作用。方法/设计:这是一项随机平行组安慰剂对照双盲临床试验。本试验招募解放军101医院(无锡太湖医院)神经外科自发性蛛网膜下腔出血患者300例。这些患者将被平等地随机分配到阿托伐他汀组(40mg /天)和安慰剂对照组。结果将在出血后的基线、3、5和14天以及出院后6个月进行评估。主要结果将是计算机断层扫描(CT)血管造影结合CT灌注成像和常规CT的结果。次要结果将是脑脊液分析、血液检测(肿瘤坏死因子α、血管内皮生长因子、白细胞介素-6和c反应蛋白水平)、Hunt-Hess分级、经颅多普勒超声检查结果、格拉斯哥昏迷评分、格拉斯哥结局评分和美国国立卫生研究院卒中评分。讨论:本试验结果将为阿托伐他汀在自发性蛛网膜下腔出血急性期的临床应用及神经再生效果提供数据。试验注册:该试验于2014年5月18日在中国临床试验注册中心(ChiCTR-IPR-14005395)注册。
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Atorvastatin for treating spontaneous subarachnoid hemorrhage: study protocol for a randomized double-blind placebo-controlled trial
Background: Animal studies have confirmed that statins have neuroprotective effects during and following a subarachnoid hemorrhage; however, the therapeutic effect of statins in humans remains controversial. The interpretation of data currently available on the clinical application of statins to spontaneous subarachnoid hemorrhage is limited by the small sample sizes used in the studies, making it difficult to draw valid conclusions regarding the multiple neuroprotective effects of statins. Thus, we propose to perform a randomized double-blind placebo-controlled parallel-group clinical trial to determine the effects of atorvastatin on spontaneous subarachnoid hemorrhage, apoptosis-related factors, and serum inflammatory factors in cerebrospinal fluid and to observe its neuroprotective effect mediated by relieving vasospasm. Methods/Design: This is a randomized parallel-group placebo-controlled double-blind clinical trial. This trial will recruit 300 patients with spontaneous subarachnoid hemorrhage from the Department of Neurosurgery, 101 st Hospital of PLA (Wuxi Taihu Hospital). These patients will be equally and randomly assigned to atorvastatin (40 mg/day) and placebo control groups. Outcomes will be evaluated at baseline, 3, 5, and 14 days after hemorrhage, and 6 months after discharge. The primary outcomes will be the results of computed tomography (CT) angiography combined with CT perfusion imaging and conventional CT. The secondary outcomes will be cerebrospinal fluid analysis, blood testing (tumor necrosis factor α, vascular endothelial growth factor, interleukin-6, and C-reactive protein levels), and the Hunt-Hess classification, the results of transcranial Doppler ultrasonography, and the scores on the Glasgow Coma Scale, the Glasgow Outcome Scale, and the National Institutes of Health Stroke Scale. Discussion: The results of this trial will provide data on the clinical application and neuroregenerative effect of atorvastatin in the acute stage of spontaneous subarachnoid hemorrhage. Trial registration: This trial was registered with the Chinese Clinical Trial Registry (ChiCTR-IPR-14005395) on 18 May 2014.
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