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Mistletoe Preparation Iscador: Are there Methodological Concerns with Respect to Controlled Clinical Trials?*

机译:槲寄生制备Iscador:是否有关于对照临床试验的方法论问题?*

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摘要

In Europe many cancer patients use complementary therapies, particularly mistletoe. Only a few controlled clinical trials have been performed with the mistletoe preparation Iscador as a complementary treatment for cancer, many of them with medium to low quality due to methodological shortcomings. Reasons for some quality concerns, particularly discontinuation of treatment and/or participation and premature termination are analyzed. Analysis is based on controlled clinical trials dealing with Iscador. Data stem from the archive of published and ongoing research of the «Verein für Krebsforschung» (Society for Cancer Research) in Arlesheim, Switzerland. Controlled clinical studies with cancer patients that were started after 01.01.1990 or were not completed by then have been evaluated. Fifty-six controlled studies are documented, 24 of them randomized and 32 non-randomized. Nine of the randomized studies were done by matched-pair design, the others by conventional parallel group design; six of the last were terminated prematurely primarily for slow recruitment due to patient preferences and compliance of physicians. Patient and physician preference seem to be important factors limiting recruitment for randomized trials and hence implementation. This adds to the overall unwillingness of participation by patients with serious diseases. A well-balanced mix of designs using different research methods and outcomes is suggested combined with analyses, in countries where mistletoe therapy in general or Iscador in particular is unknown or not available.
机译:在欧洲,许多癌症患者使用辅助疗法,尤其是槲寄生。槲寄生制剂Iscador作为癌症的补充治疗仅进行了少数对照临床试验,由于方法学上的缺陷,其中许多质量中等至较低。分析了一些质量问题的原因,特别是中止治疗和/或参与以及过早终止的原因。分析基于与Iscador相关的受控临床试验。数据来自瑞士阿尔勒斯海姆的“ VereinfürKrebsforschung”(癌症研究学会)已发表和正在进行的研究档案。已评估了1990年1月1日之后开始或尚未完成的癌症患者对照临床研究。记录了56项对照研究,其中24项为随机研究,32项为非随机研究。随机研究中有九项是通过配对配对设计完成的,其他则是通过常规平行组设计完成的;最后六个中的六个被提前终止,主要是由于患者的喜好和医生的依从性而导致招聘缓慢。患者和医生的偏好似乎是限制招募随机试验并因此限制实施的重要因素。这增加了患有严重疾病的患者总体上不愿参加的意愿。建议在一般槲寄生疗法或特别是Iscador未知或无法获得的国家中,采用不同的研究方法和结果,将设计均衡地结合在一起进行分析。

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  • 作者

    Ziegler, Renatus;

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  • 年度 2009
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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