Design and Analysis of Cross-Over Trials, Second Edition

الغلاف الأمامي
CRC Press, 12‏/03‏/2003 - 408 من الصفحات

The first edition of Design and Analysis of Cross-Over Trials quickly became the standard reference on the subject and has remained so for more than 12 years. In that time, however, the use of cross-over trials has grown rapidly, particularly in the pharmaceutical arena, and researchers have made a number of advances in both the theory and methods applicable to these trials.

Completely revised and updated, the long-awaited second edition of this classic text retains its predecessor's careful balance of theory and practice while incorporating new approaches, more data sets, and a broader scope. Enhancements in the second edition include:

  • A new chapter on bioequivalence
  • Recently developed methods for analyzing longitudinal continuous and categorical data
  • Real-world examples using the SAS system
  • A comprehensive catalog of designs, datasets, and SAS programs available on a companion Web site at www.crcpress.com

The authors' exposition gives a clear, unified account of the design and analysis of cross-over trials from a statistical perspective along with their methodological underpinnings. With SAS programs and a thorough treatment of design issues, Design and Analysis of Cross-Over Trials, Second Edition sets a new standard for texts in this area and undoubtedly will be of direct practical value for years to come.

 

المحتوى

1 Introduction
1
2 The 22 CrossOver Trial
11
3 HigherOrder Designs for Two Treatments
114
4 Designs for three or more treatments
146
5 Analysis of continuous data
193
6 Analysis of categorical data
267
7 Bioequivalence trials
305
Appendix A Least squares estimation
333
Appendix B SAS code for assessing ABE IBE and PBE in replicate crossover trials
338
References
342
Index
355

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