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portada Handbook of Statistical Methods for Randomized Controlled Trials (Chapman & Hall (in English)
Type
Physical Book
Publisher
Language
Inglés
Pages
620
Format
Paperback
Dimensions
25.4 x 17.8 x 3.4 cm
Weight
1.12 kg.
ISBN13
9781032009100
Edition No.
1

Handbook of Statistical Methods for Randomized Controlled Trials (Chapman & Hall (in English)

Kyungmann Kim (Illustrated by) · Frank Bretz (Illustrated by) · Ying Kuen K. Cheung (Illustrated by) · CRC Press · Paperback

Handbook of Statistical Methods for Randomized Controlled Trials (Chapman & Hall (in English) - Kim, Kyungmann ; Bretz, Frank ; Cheung, Ying Kuen K.

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Synopsis "Handbook of Statistical Methods for Randomized Controlled Trials (Chapman & Hall (in English)"

Statistical concepts provide scientific framework in experimental studies, including randomized controlled trials. In order to design, monitor, analyze and draw conclusions scientifically from such clinical trials, clinical investigators and statisticians should have a firm grasp of the requisite statistical concepts. The Handbook of Statistical Methods for Randomized Controlled Trials presents these statistical concepts in a logical sequence from beginning to end and can be used as a textbook in a course or as a reference on statistical methods for randomized controlled trials.Part I provides a brief historical background on modern randomized controlled trials and introduces statistical concepts central to planning, monitoring and analysis of randomized controlled trials. Part II describes statistical methods for analysis of different types of outcomes and the associated statistical distributions used in testing the statistical hypotheses regarding the clinical questions. Part III describes some of the most used experimental designs for randomized controlled trials including the sample size estimation necessary in planning. Part IV describe statistical methods used in interim analysis for monitoring of efficacy and safety data. Part V describe important issues in statistical analyses such as multiple testing, subgroup analysis, competing risks and joint models for longitudinal markers and clinical outcomes. Part VI addresses selected miscellaneous topics in design and analysis including multiple assignment randomization trials, analysis of safety outcomes, non-inferiority trials, incorporating historical data, and validation of surrogate outcomes.

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All books in our catalog are Original.
The book is written in English.
The binding of this edition is Paperback.

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