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EuroHYP-1: European multicenter, randomized, phase III clinical trial of therapeutic hypothermia plus best medical treatment vs. best medical treatment alone for acute ischemic stroke.

机译:EuroHYP-1:治疗急性低温的欧洲多中心,随机,III期临床试验,包括低温治疗,最佳药物治疗与最佳药物治疗。

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摘要

Cooling reduced infarct size and improved neurological outcomes in animal studies modeling ischemic stroke, and also improved outcome in randomized clinical trials in patients with hypoxic-ischemic brain injury after cardiac arrest. Cooling awake patients with ischemic stroke has been shown feasible in phase II clinical trials.To determine whether systemic cooling to a target body temperature between 34·0 and 35·0°C, started within six-hours of symptom onset and maintained for 24 h, improves functional outcome at three-months in patients with acute ischemic stroke.International, multicenter, phase III, randomized, open-label clinical trial with blinded outcome assessment in 1500 patients aged 18 years or older with acute ischemic stroke and a National Institutes of Health Stroke Scale score of 6 up to and including 18. In patients randomized to hypothermia, cooling to a target body temperature of 34-35°C will be started within six-hours after symptom onset with rapid intravenous infusion of refrigerated normal saline or a surface cooling technique and maintained for 24 h with a surface or endovascular technique. Patients randomized to hypothermia will receive pethidine and buspirone to prevent shivering and discomfort.Score on the modified Rankin Scale at 91 days, as analyzed with ordinal logistic regression and expressed as a common odds ratio.With 750 patients per intervention group, this trial has 90\% power to detect 7\% absolute improvement at the 5\% significance level. The full trial protocol is available at http://www.eurohyp1.eu. ClinicalTrials.gov Identifier: NCT01833312.
机译:在模拟缺血性中风的动物研究中,降温可减少梗塞面积并改善神经系统结局,并且在心脏骤停后低氧缺血性脑损伤患者的随机临床试验中,结局也得到改善。在II期临床试验中证明为清醒的缺血性中风患者降温是可行的。确定是否在症状发作后六小时内开始将全身降温至目标体温在34·0至35·0°C之间并维持24小时可以改善急性缺血性中风患者三个月的功能结局。国际,多中心,III期,随机,开放标签临床试验对1500名18岁以上的急性缺血性中风患者和美国国立卫生研究院进行了盲法结局评估Health Stroke Scale评分为6(最高),包括18。在随机接受低温治疗的患者中,症状发作后的六小时内应开始冷却至目标体温34-35°C,并迅速静脉输注冷冻的生理盐水或表面冷却技术,并通过表面或血管内技术维持24小时。随机接受低温治疗的患者将接受哌替啶和丁螺环酮预防发抖和不适.91天时采用改良的Rankin量表评分,经序数Logistic回归分析并以常见优势比表示。每个干预组有750名患者,该试验有90名患者在显着性水平为5%的情况下,具有7%的绝对功率检测能力。完整的试用协议可从http://www.eurohyp1.eu获得。 ClinicalTrials.gov标识符:NCT01833312。

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