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关于新型抗精神病药物治疗双相情感障碍急性躁狂期的对照临床试验的报告质量

Quality of reporting controlled clinical trials on treatment of the acute mania phase of bipolar disorder with new antipsychotic drugs.

作者信息

Arbaizar B, Gómez-Acebo I, Llorca J

机构信息

Hospital de Laredo, Cantabria, Spain.

出版信息

Pharmacopsychiatry. 2008 Nov;41(6):240-1. doi: 10.1055/s-0028-1083817. Epub 2008 Dec 9.

Abstract

The main goal in this paper is to describe how articles on clinical trials on atypical antipsychotic drugs in bipolar disorder reported their design. 25 controlled clinical trials were identified. Data were extracted on the general characteristics of the studies, including sources of funding, study design, and ethical issues. Most trials adequately report design issues such as patient selection, randomization, and flow of patients. However, only 8 of 25 studies reported pre-estimation of sample size; 22 articles claimed a double-blind design, but only 3 reported details on how blinding was performed; 17 trials failed to explicitly adhere to the Declaration of Helsinki.

摘要

本文的主要目标是描述关于双相情感障碍非典型抗精神病药物临床试验的文章如何报告其设计。共识别出25项对照临床试验。提取了关于研究一般特征的数据,包括资金来源、研究设计和伦理问题。大多数试验充分报告了设计问题,如患者选择、随机化和患者流程。然而,25项研究中只有8项报告了样本量的预先估计;22篇文章声称采用双盲设计,但只有3篇报告了关于如何实施盲法的细节;17项试验未能明确遵守《赫尔辛基宣言》。

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