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首页> 外文期刊>Trials >Study of therapeutic hypothermia (32 to 35°C) for intracranial pressure reduction after traumatic brain injury (the Eurotherm3235Trial): outcome of the pilot phase of the trial
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Study of therapeutic hypothermia (32 to 35°C) for intracranial pressure reduction after traumatic brain injury (the Eurotherm3235Trial): outcome of the pilot phase of the trial

机译:治疗低温(32至35°C)以降低颅脑外伤后颅内压的研究(Eurotherm3235Trial):该试验性试验阶段的结果

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Background Clinical trials in traumatic brain injury (TBI) are challenging. Previous trials of complex interventions were conducted in high-income countries, reported long lead times for site setup and low screened-to-recruitment rates. In this report we evaluate the internal pilot phase of an international, multicentre TBI trial of a complex intervention to assess: design and implementation of an online case report form; feasibility of recruitment (sites and patients); feasibility and effectiveness of delivery of the protocol. Methods All aspects of the pilot phase of the trial were conducted as for the main trial. The pilot phase had oversight by independent Steering and Data Monitoring committees. Results Forty sites across 12 countries gained ethical approval. Thirty seven of 40 sites were initiated for recruitment. Of these, 29 had screened patients and 21 randomized at least one patient. Lead times to ethics approval (6.8 weeks), hospital approval (18 weeks), interest to set up (61 weeks), set up to screening (11 weeks), and set up to randomization (31.6 weeks) are comparable with other international trials. Sixteen per cent of screened patients were eligible. We found 88% compliance rate with trial protocol. Conclusion The pilot data demonstrated good feasibility for this large international multicentre randomized controlled trial of hypothermia to control intracranial pressure. The sample size was reduced to 600 patients because of homogeneity of the patient group and we showed an optimized cooling intervention could be delivered. Trial registration Current Controlled Trials: ISRCTN34555414 .
机译:背景技术在创伤性脑损伤(TBI)中的临床试验具有挑战性。先前在高收入国家进行了复杂干预措施的试验,报道了现场设置的准备时间长且筛选后招聘率低。在本报告中,我们评估了一项复杂干预措施的国际,多中心TBI试验的内部试验阶段,以评估:设计和实施在线病例报告表;招聘的可行性(地点和患者);协议交付的可行性和有效性。方法本试验的试验阶段的各个方面均与主要试验相同。试点阶段由独立的指导和数据监控委员会进行监督。结果12个国家/地区的40个地点获得了道德认可。已启动40个站点​​中的37个以进行招聘。其中,有29名接受过筛查的患者和21名随机分配的至少一名患者。伦理批准的准备时间(6.8周),医院批准的时间(18周),建立兴趣的时间(61周),建立筛查的时间(11周)和建立随机性的时间(31.6周)与其他国际试验相当。接受筛查的患者中有16%符合条件。我们发现试验方案的符合率为88%。结论初步数据证明了这项针对体温过低的大型国际多中心随机对照试验以控制颅内压的良好可行性。由于患者组的同质性,样本量减少到600名患者,我们证明可以提供优化的降温干预措施。试用注册当前控制的试用:ISRCTN34555414。

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