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Minimal sufficient balance randomization for sequential randomized controlled trial designs: results from the ESCAPE trial

机译:连续随机对照试验设计的最小平衡平衡随机数:ESCAPE试验的结果

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We describe the implementation of minimal sufficient balance randomization, a covariate-adaptive randomization technique, used for the “Endovascular treatment for Small Core and Anterior circulation Proximal occlusion with Emphasis on minimizing CT to recanalization times” (ESCAPE) trial. The ESCAPE trial is a prospective, multicenter, randomized clinical trial that enrolled subjects with the following main inclusion criteria: less than 12?h from symptom onset, age 18?years or older, baseline NIHSS score?>?5, ASPECTS score?>?5 and computed tomography angiography (CTA) evidence of carotid T/L or M1-segment middle cerebral artery (MCA) occlusion, and at least moderate collaterals by CTA. Patients were randomized using a real-time, dynamic, Internet-based, minimal sufficient balance randomization method that balanced the study arms with respect to baseline covariates including age, sex, baseline NIHSS score, site of arterial occlusion, baseline ASPECTS score and treatment with intravenously administered alteplase. Permutation-based tests of group differences confirmed group balance across several baseline covariates including sex (p?=?1.00), baseline NIHSS score (p?=?0.95), site of arterial occlusion (p?=?1.00), baseline ASPECTS score (p?=?0.28), treatment with intravenously administered alteplase (p?=?0.31), and age (p?=?0.67). Results from the ESCAPE trial demonstrate the feasibility and the benefit of this covariate adaptive randomization scheme in small-sample trials and for data monitoring endeavors. ESCAPE trial – NCT01778335 – at www.clinicaltrials.gov . Registered on 29 January 2013.
机译:我们描述了一种最小的足够平衡随机化的实现方法,该方法是一种协变量自适应随机化技术,用于“小核和前循环近端闭塞的血管内治疗,重点是将CT最小化至再通时间”(ESCAPE)试验。 ESCAPE试验是一项前瞻性,多中心,随机临床试验,纳入了以下主要纳入标准的受试者:症状发作后12小时以内,年龄18岁或以上,基线NIHSS得分≥5,ASPECTS得分? ?5和计算机断层摄影血管造影(CTA)证明颈动脉T / L或M1段大脑中动脉(MCA)闭塞,以及CTA至少有中等程度的侧支。使用实时,动态,基于互联网的,最低限度的充分平衡随机化方法对患者进行随机化,该方法可就基线协变量,包括年龄,性别,基线NIHSS得分,动脉闭塞部位,基线ASPECTS得分以及静脉给予阿替普酶。基于组差异的基于排列的检验确认了多个基线协变量之间的组平衡,包括性别(p?=?1.00),基线NIHSS评分(p?=?0.95),动脉闭塞部位(p?=?1.00),基线ASPECTS评分(p = 0.28),静脉注射阿替普酶(p = 0.31),年龄(p = 0.67)。 ESCAPE试验的结果证明了这种协变量自适应随机方案在小样本试验和数据监测方面的可行性和益处。 ESCAPE试用版– NCT01778335 –在www.clinicaltrials.gov上。 2013年1月29日注册。

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