10% off all books and free delivery over £40
Buy from our bookstore and 25% of the cover price will be given to a school of your choice to buy more books. *15% of eBooks.

Statistical Thinking in Clinical Trials

View All Editions (4)

The selected edition of this book is not available to buy right now.
Add To Wishlist
Write A Review

About

Statistical Thinking in Clinical Trials Synopsis

Statistical Thinking in Clinical Trials combines a relatively small number of key statistical principles and several instructive clinical trials to gently guide the reader through the statistical thinking needed in clinical trials. Randomization is the cornerstone of clinical trials and randomization-based inference is the cornerstone of this book. Read this book to learn the elegance and simplicity of re-randomization tests as the basis for statistical inference (the analyze as you randomize principle) and see how re-randomization tests can save a trial that required an unplanned, mid-course design change.

Other principles enable the reader to quickly and confidently check calculations without relying on computer programs. The `EZ' principle says that a single sample size formula can be applied to a multitude of statistical tests. The `O minus E except after V' principle provides a simple estimator of the log odds ratio that is ideally suited for stratified analysis with a binary outcome. The same principle can be used to estimate the log hazard ratio and facilitate stratified analysis in a survival setting. Learn these and other simple techniques that will make you an invaluable clinical trial statistician.

About This Edition

ISBN: 9781138058569
Publication date:
Author: Michael A Proschan
Publisher: Chapman & Hall/CRC an imprint of CRC Press
Format: Paperback
Pagination: 264 pages
Series: Chapman & Hall/CRC Biostatistics Series
Genres: Biology, life sciences
Clinical trials
Epidemiology and Medical statistics
Pharmaceutical chemistry and technology
Probability and statistics