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Design and Analysis of Cross-Over Trials, Sec... by Kenward, Michael G. Hardback

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Condition
Good
A book that has been read but is in good condition. Very minimal damage to the cover including scuff marks, but no holes or tears. The dust jacket for hard covers may not be included. Binding has minimal wear. The majority of pages are undamaged with minimal creasing or tearing, minimal pencil underlining of text, no highlighting of text, no writing in margins. No missing pages. See the seller’s listing for full details and description of any imperfections. See all condition definitionsopens in a new window or tab
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“good condition”
ISBN
0412606402
EAN
9780412606403
Release Title
Design and Analysis of Cross-Over Trials, Second Edition (Chap...
Artist
Kenward, Michael G.
Brand
N/A
Colour
N/A
Book Title
Design and Analysis of Cross-Over Trials, Second Edition (Chap...
Subject Area
Mathematics, Medical
Publication Name
Design and Analysis of Cross-Over Trials
Item Length
9.1 in
Publisher
CRC Press LLC
Subject
Biostatistics, Probability & Statistics / General, Pharmacology
Publication Year
2003
Series
Chapman and Hall/Crc Monographs on Statistics and Applied Probability Ser.
Type
Textbook
Format
Hardcover
Language
English
Item Height
1.1 in
Author
Byron Jones, Michael G. Kenward
Item Width
6.3 in
Item Weight
24.1 Oz
Number of Pages
408 Pages

About this product

Product Information

The first edition of Design and Analysis of Cross-Over Trialsquickly 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.

Product Identifiers

Publisher
CRC Press LLC
ISBN-10
0412606402
ISBN-13
9780412606403
eBay Product ID (ePID)
2040808

Product Key Features

Author
Byron Jones, Michael G. Kenward
Publication Name
Design and Analysis of Cross-Over Trials
Format
Hardcover
Language
English
Subject
Biostatistics, Probability & Statistics / General, Pharmacology
Publication Year
2003
Series
Chapman and Hall/Crc Monographs on Statistics and Applied Probability Ser.
Type
Textbook
Subject Area
Mathematics, Medical
Number of Pages
408 Pages

Dimensions

Item Length
9.1 in
Item Height
1.1 in
Item Width
6.3 in
Item Weight
24.1 Oz

Additional Product Features

Edition Number
2
LCCN
2002-041503
Intended Audience
Scholarly & Professional
Series Volume Number
98
Lc Classification Number
R853.C76j66 2003
Edition Description
Revised Edition,New Edition
Table of Content
INTRODUCTION What is a Cross-Over Trial? With which Sort of Cross-Over Trial are We Concerned? Why Do Cross-Over Trials Need Special Consideration? A Brief History Notation, Models and Analysis Aims of this Book Structure of the Book THE 2 x 2 CROSS-OVER TRIAL Introduction Plotting the Data The Analysis Using t-Tests Sample Size Calculations The Analysis of Variance Aliasing of Effects Consequences of preliminary testing Analyzing the residuals A Bayesian Analysis of the 2 x 2 Trial The Use of Baseline Measurements The Use of Covariates Nonparametric Analysis Binary Data HIGHER-ORDER DESIGNS FOR TWO TREATMENTS Introduction 'Optimal' Designs Balaam's Design for Two Treatments The Effect of Preliminary Testing in Balaam's Design Three-Period Designs with Two Sequences Three-Period Designs with Four Sequences A Three-Period Six-Sequence Design Which Three-Period Design to Use? Four-Period Designs with Two Sequences Four-Period Designs with Four Sequences Four-Period Designs with Six Sequences Which Four-Period Design to Use? Which Two-Treatment Design to Use? DESIGNING CROSS-OVER TRIALS FOR THREE OR MORE TREATMENTS Introduction Variance-Balanced Designs Optimality Results for Cross-Over Designs Which Variance Balanced Design to Use? Partially Balanced Designs Comparing Test Treatments to a Control Factorial Treatment Combinations Extending the Simple Model for Carry-Over Effects Computer Search Algorithms ANALYSIS OF CONTINUOUS DATA Introduction The Fixed Subject Effects Model The Random Subject Effects Model Analyses for Higher-Order Two-Treatment Designs The General Linear Mixed Model Analysis of Repeated Measurements within Periods Cross-Over Data as Repeated Measurements Case Study: an Analysis of a Trial with Many Periods ANALYSIS OF CATEGORICAL DATA Introduction Binary Data: Subject Effect Models Binary Data: Marginal Models Categorical Data Further Topics BIOEQUIVALENCE TRIALS What is Bioequivalence Testing for Average Bioequivalence Power and Sample Size for ABE in the 2 x 2 Design Individual Bioequivalence Population Bioequivalence ABE for a Replicate Design Kullback-Leibler Divergence for Evaluating Bioequivalence Modelling Pharmacokinetic Data APPENDICES Least Squares Estimation SAS Code for Assessing ABEm IBE, and PBE in Replicate Cross-Over Trials REFERENCES
Copyright Date
2002
Dewey Decimal
615.5/07/2
Dewey Edition
21
Illustrated
Yes

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