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首页> 外文期刊>Journal of stroke and cerebrovascular diseases: The official journal of National Stroke Association >The Clomethiazole Acute Stroke Study in Ischemic, Hemorrhagie, and t-PA Treated Stroke: Design of a Phase III Trial in the United States and Canada
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The Clomethiazole Acute Stroke Study in Ischemic, Hemorrhagie, and t-PA Treated Stroke: Design of a Phase III Trial in the United States and Canada

机译:缺血,出血和t-PA治疗的中风中的氯甲唑急性中风研究:美国和加拿大的III期试验设计

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Clomethiazole is a drug with sedative properties effective in laboratory studies of brain ischemia. A large European multicenter trial of Clomethiazole in acute stroke patients showed no benefit overall, but subgroup analysis indicated that patients with large infarctions may have benefited from treatment. To confirm this preliminary finding, we have designed CLASS-IHT, the Clomethiazole for Acute Stroke Study in Ischemic, Hemorrhagic and TPA Treated Patients, to be conducted in North America. Patients who suffer large cerebral infarctions and present within 12 hours of symptom onset are eligible. Patients will be randomized to receive Clomethiazole 68 mg/kg over 24 hours or vehicle, using a dosing scheme based on the pharmaco-kinetics measured in the first trial. Outcome assessments include stroke scales, the Barthel Index, and lesion volume. An additional study of health economic outcomes is planned. The primary endpoint for CLASS-I will be the Barthel Index 90 days after stroke. A total of 1,200 patients will be randomized to CLASS-I, and in safety-only trials, 200 patients with cerebral hemorrhage will be randomized into CLASS-H and another 100 to 200 patients will be randomized into CLASS-T. The details of the protocols for all three studies are presented.
机译:克罗米唑是一种具有镇静作用的药物,在脑缺血的实验室研究中有效。欧洲一项大型的氯吡唑对急性卒中患者的多中心试验显示总体上没有益处,但亚组分析表明,大面积梗死的患者可能从治疗中受益。为了证实这一初步发现,我们设计了CLASS-IHT,这是一种在缺血,出血和TPA治疗的患者中用于急性卒中研究的氯甲唑。患有严重脑梗塞且在症状发作后12小时内出现的患者是合格的。使用基于第一次试验中测得的药代动力学的给药方案,患者将在24小时或溶媒中随机分配接受68 mg / kg的氯甲咪唑。结果评估包括卒中量表,Barthel指数和病变体积。计划对卫生经济成果进行另一项研究。 CLASS-I的主要终点是卒中后90天的Barthel指数。总共1200名患者将被随机分入CLASS-I,在仅安全性试验中,200名脑出血患者将被随机分为CLASS-H,另外100至200名患者将被随机分为CLASS-T。提出了所有三个研究的协议的细节。

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