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用于评估治疗的研究设计。

Study design for the evaluation of treatment.

作者信息

Morales A J

机构信息

Department of Reproductive Medicine, University of California, San Diego, La Jolla, USA.

出版信息

Semin Reprod Endocrinol. 1996 May;14(2):111-8. doi: 10.1055/s-2007-1016318.

Abstract

Study design is a critical step in clinical research. Such studies may be either randomized or nonrandomized; the latter may be retrospective or prospective. Nonrandomized designs include surveys and observational studies. The randomized clinical trial (RCT) is an experimental design, with patients randomly allocated to treatment arms. A number of designs are possible. These include the simple experiment, repeated measure design, crossover study, and factorial design. Issues in clinical trials include subject inclusion/exclusion criteria, control group treatment, blinding, compliance, sample size, treatment assignment, and subject withdrawal. Disadvantages of the RCT include cost and the lack of true clinical equipoise. It is also worth noting that the RCT is not infallible. Patients should be analyzed based not on their compliance but rather on an intent-to-treat basis.

摘要

研究设计是临床研究中的关键步骤。此类研究可以是随机的或非随机的;后者可以是回顾性的或前瞻性的。非随机设计包括调查和观察性研究。随机临床试验(RCT)是一种实验设计,患者被随机分配到各治疗组。有多种设计可能。这些包括简单实验、重复测量设计、交叉研究和析因设计。临床试验中的问题包括受试者纳入/排除标准、对照组治疗、盲法、依从性、样本量、治疗分配和受试者退出。RCT的缺点包括成本和缺乏真正的临床均衡性。还值得注意的是,RCT并非绝对可靠。患者应基于意向性治疗而非依从性进行分析。

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