Books+ Search Results

Statistics Applied to Clinical Trials

Title
Statistics Applied to Clinical Trials [electronic resource] / by Ton J. Cleophas, Aeilko H. Zwinderman, Toine F. Cleophas.
ISBN
9789401003377
Edition
Second Edition.
Published
Dordrecht : Springer Netherlands : Imprint: Springer, 2002.
Physical Description
1 online resource.
Local Notes
Access is available to the Yale community.
Access and use
Access restricted by licensing agreement.
Summary
In 1948 the first randomized controlled trial was published by the English Medical Research Council in the <em>British Medical Journal</em>. Until then, observations had been uncontrolled. Initially, trials frequently did not confirm hypotheses to be tested. This phenomenon was attributed to low sensitivity due to small samples, as well as inappropriate hypotheses based on biased prior trials. Additional flaws were recognized and subsequently were better accounted for: carryover effects due to insufficient washout from previous treatments, time effects due to external factors and the natural history of the condition under study, bias due to asymmetry between treatment groups, lack of sensitivity due to a negative correlation between treatment responses, etc. Such flaws, mainly of a technical nature, have been largely corrected and led to trials after 1970 being of significantly better quality than before. The past decade has focused, in addition to technical aspects, on the need for circumspection in planning and conducting of clinical trials. As a consequence, prior to approval, clinical trial protocols are now routinely scrutinized by different circumstantial bodies, including ethics committees, institutional and federal review boards, national and international scientific organizations, and monitoring committees charged with conducting interim analyses. <br/> This book not only explains classical statistical analyses of clinical trials, but addresses relatively novel issues, including equivalence testing, interim analyses, sequential analyses, and meta-analyses, and provides a framework of the best statistical methods currently available for such purposes. The book is not only useful for investigators involved in the field of clinical trials, but also for all physicians who wish to better understand the data of trials as currently published.
Variant and related titles
Springer ebooks.
Other formats
Printed edition:
Format
Books / Online
Language
English
Added to Catalog
February 06, 2013
Contents
Preface
Foreword
1. Hypotheses, Data, Stratification
2. The analysis of efficacy data of drug trials
3. The analysis of safety data of drug trials
4. Equivalence testing
5. Statistical power and sample size
6. Interim analysis
7. Multiple statistical inferences
8. Principles of linear regression
9. Subgroup analysis multiple linear regression: confounding, interaction, synergism
10. Curvilinear regression
11. Meta-analysis
12. Crossover studies with continuous variables: power analysis
13. Crossover studies with binary responses
14. Post-hoc analysis in clinical trials, a case for logistic regression analysis
15. quality-of-life assessment in clinical trials
16. Statistics for the analysis of genetic data
17. Relationship among statistical distributions
18. Statistics is not "bloodless" algebra
Appendix
Index.
Subjects
Also listed under
Zwinderman, Aeilko H.
Cleophas, Toine F.
SpringerLink (Online service)
Citation

Available from:

Loading holdings.
Unable to load. Retry?
Loading holdings...
Unable to load. Retry?