针灸科
指南
医学
临床试验
随机对照试验
食品药品监督管理局
替代医学
研究设计
临床研究设计
临床研究
物理疗法
医学物理学
药理学
外科
病理
社会科学
社会学
作者
Haiyong Chen,Mingxiao Yang,Zhipeng Ning,Wing Lok Lam,Ying Zhao,Wing‐Fai Yeung,Bacon Fung Leung Ng,Eric Tat-Chi Ziea,Lixing Lao
标识
DOI:10.1142/s0192415x19500010
摘要
Guidelines for clinical trials of acupuncture are scarce, particularly in their guidance on choosing an adequate control in an acupuncture trial. This guideline was developed to address the research methodology for clinical research in acupuncture which contains the essential elements to be considered in the design, preparation and reporting of an acupuncture RCT. Particularly, investigators focused on the control design because of the unique feature of acupuncture. As one size does not fit all, one single design cannot answer all research questions. Therefore, we recommend that the clinical questions be answered in different stages of trials by choosing the appropriate control or comparator. This concept is adapted from classical drug trials developed by the Food and Drug Administration (FDA) of USA in which trials are staged in four phages in order to address different research questions. From the points listed above, this guideline offers the specific recommendations in an acupuncture RCT.
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