首页> 外文期刊>Stem cells international >Improving Stem Cell Clinical Trial Design and Conduct: Development of a Quality Assessment Tool for Stem Cell Clinical Trials
【24h】

Improving Stem Cell Clinical Trial Design and Conduct: Development of a Quality Assessment Tool for Stem Cell Clinical Trials

机译:改善干细胞临床试验设计和行为:干细胞临床试验的质量评估工具的开发

获取原文
           

摘要

Background. Clinical trials are at the cornerstone of evidence-based stem cell therapies, but the quality assessment for designing and conduct these sometimes-complex studies are scarce of evidence. This study is aimed at developing a handy quality assessment tool for stem cell clinical trials, enhancing capacity of the self-regulate overall quality, and participating protection. Methods. The framework of quality assessment tool was based on the PQRS (progress-quality-regulation-scientific) quality assessment tool, and detailed quality indicators were developed by leader group discussion, expert consulting, and literature review. Stem cell clinical trials were retrieved from the International Clinical Trials Registry Platform, and corresponding quality indicators were assessed and extracted. The validity and feasibility of conceptual quality assessment tool were further evaluated by using structural equation modeling. Results. The quality assessment tool for stem cell clinical trials contains four critical quality attributes, including participant protection, scientific value, quality control, and stem cell products, and 9 observed quality indicators. From 11 primary clinical trial registries in the International Clinical Trials Registry Platform, 9410 stem cell trial registrations were identified, and 1036 studies were eligible for publications and protocols screening. After reviewed full text, 37 studies were included in the validity and feasibility evaluation: 32 studies were completed, and 3 studies terminated early. Most of the studies (83.79%) were in the early phase, and 63.16% of the studies were investigator-initiated trial. To further tested for validity, the critical quality attributes and quality indicators (QIs) between expertise further validated by the SEM method, which showed a good fit for the model (chi?square=26.008; P=0.353; TLI=0.967; CFI=0.978; RMSEA=0.048). Compared with exploratory trials, evaluating using the quality assessment tool, confirmatory trials performed similarly in participant protection, scientific value, and quality control, but lower in stem cell products. Conclusions. The results of critical quality attributes and quality indicators between expertise and confirmatory validation analysis are basically consistent, indicating the feasibility and validity of applying this quality assessment tool for overall quality evaluation of stem cell trials.
机译:背景。临床试验处于基于证据的干细胞疗法的基石,但设计和进行这些有时复杂的研究的质量评估是稀缺证据。本研究旨在为干细胞临床试验开发一种方便的质量评估工具,增强了自我规范的整体质量和参与保护的能力。方法。质量评估工具的框架是基于PQRS(进度 - 质量调节科学)质量评估工具,并通过领导集团讨论,专家咨询和文学审查制定了详细的质量指标。从国际临床试验登记平台中检索干细胞临床试验,并评估和提取相应的质量指标。采用结构方程建模进一步评估了概念质量评估工具的有效性和可行性。结果。干细胞临床试验的质量评估工具含有四个关键质量属性,包括参与者保护,科学价值,质量控制和干细胞产品,以及9个观察到的质量指标。从11个主要临床试验登记处在国际临床试验登记平台中,确定了9410个干细胞试验登记,并有资格获得出版物和审议筛选的1036项研究。在审查全文后,有效性和可行性评估中包含37项研究:32项研究完成,早期终止了3项研究。大多数研究(83.79%)在早期阶段,63.16%的研究是调查员启动的试验。为了进一步测试有效性,通过SEM方法进一步验证的专业知识之间的临界质量属性和质量指标(QIS),这表明了型号的良好贴合(Chi?Square = 26.008; P = 0.353; TLI = 0.967; CFI = 0.978; rmsea = 0.048)。与探索性试验相比,使用质量评估工具进行评估,确认试验在参与者保护,科学价值和质量控制中同样进行,但干细胞产品中较低。结论。专业知识和确认验证分析之间的关键质量属性和质量指标的结果基本一致,表明应用这种质量评估工具的可行性和有效性,以便为干细胞试验的整体质量评估。

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