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Clinical trial registration and publication of randomized controlled trials.

机译:临床试验注册和随机对照试验的发表。

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In Reply: Dr Lash raises the issue of the independent trial assumption in determining our study power. He also requests the presentation of outcomes limited only to the person-time that had not been included in the earlier reports, to support meta-analysis. Our patient cohort did include some cases previously reported (22% of the overall cohort). However, as noted in the article, their use was based on a longer clinical follow-up and expansion of the genotyping to include multiple alleles *3, *4, *10, and *41. We agree that these cases cannot be viewed as completely independent, yet, because of the extended follow-up and new data with newly assigned CYP2D6 alleles, any distinction between previous and current person-time is not feasible.
机译:在答复中:拉什博士在确定我们的研究能力时提出了独立试验假设的问题。他还要求仅限于早期报告中未提及的个人时间的结果介绍,以支持荟萃分析。我们的患者队列确实包括先前报道的一些病例(占总队列的22%)。但是,如本文所述,它们的使用是基于更长的临床随访和基因分型的扩展,以包括多个等位基因* 3,* 4,* 10和* 41。我们同意,不能将这些病例视为完全独立的,但是,由于扩展的随访和具有新分配的CYP2D6等位基因的新数据,在以前和现在的人时之间进行任何区分都是不可行的。

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