Titlebook: Randomised Controlled Clinical Trials; Christopher J. Bulpitt Book 1983 Springer Science+Business Media Dordrecht 1983 experiment

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Book 1983 [1]. This definition specifies a careful design and requires the provision of adequate controls. Random allocation of treatments to subjects is important to ensure is entitled that the treated and control groups are similar. Therefore this book Randomised Controlled Clinical Trials. We can define a

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Information to be Collected during a Trial, defaulters and the attempts made to contact them. This chapter also considers the quantity of data to be collected, the design of documents, the questions to be asked, and the various stages of data preparation.

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Failure to Accept the Results of Randomised Controlled Trials,ely accepted and also three series of trials on related drugs, the collective results of which are difficult to interpret. After discussing these trials, we shall return to the reasons for rejecting the results of a randomised controlled trial.

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Book 1983book is directed primarily at the medical research worker, although certain chapters may find a wider application. When discussing a randomised controlled trial, it is neither practicable nor desirable to divorce theory from practice, however the first ten chapters con­ centrate mainly on theory, an

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