首页> 外文期刊>Pediatric Investigation >Critical components for designing and implementing randomized controlled trials
【24h】

Critical components for designing and implementing randomized controlled trials

机译:设计和实施随机对照试验的关键组件

获取原文
       

摘要

Randomized controlled trials (RCTs) are considered the first level of evidence to assess the efficacy of novel interventions/therapies. Proper design and implementation of an RCT can result in convincing causal inferences. RCTs often represent the gold standard for clinical trials when appropriately designed, conducted and reported. However, there are limitations in implementation of RCTs, including sufficiency of randomized allocation (especial for allocation concealment), implementing standard intervention, maintaining follow‐up and statement of conflicting interests. Therefore, the basic principles of RCTs are outlined here so that pediatric investigators can further understand what is the best evidence based on RCTs. More importantly, the quality of pediatric RCTs may be improved by following challenges in pediatric clinical trials outlined here.
机译:随机对照试验(RCT)被认为是评估新型干预措施/疗法功效的第一级证据。正确设计和实施RCT可以令人信服地推论因果关系。如果适当地设计,实施和报告,RCT通常代表临床试验的黄金标准。但是,RCT的实施存在局限性,包括随机分配的充分性(尤其是隐藏分配),实施标准干预,维持后续行动和利益冲突声明。因此,这里概述了RCT的基本原理,以便儿科研究者可以进一步了解什么是基于RCT的最佳证据。更重要的是,通过遵循此处概述的儿科临床试验中的挑战,可以提高儿科RCT的质量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号