SAS 关于临床试验设计,分析,报告的经典书:Contents
Introduction xii
Part I: Fundamentals of Trial Design
Chapter 1 Randomized Clinical Trials 1
Chapter 2 Uncontrolled Trials 15
Chapter 3 Protocol Development 23
Chapter 4 Endpoints 37
Chapter 5 Patient Selection 47
Chapter 6 Source and Control of Bias 55
Chapter 7 Randomization 65
Chapter 8 Blinding 75
Chapter 9 Sample Size and Power 81
Part II: Alternative Trial Designs
Chapter 10 Crossover Trials 91
Chapter 11 Factorial Design 101
Chapter 12 Equivalence Trials 113
Chapter 13 Bioequivalence Trials 119
Chapter 14 Noninferiority Trials 131
Chapter 15 Cluster Randomized Trials 141
Chapter 16 Multicenter Trials 153
Part III: Basics of Statistical Analysis
Chapter 17 Types of Data and Normal Distribution 167
Chapter 18 Significance Tests and Confidence Intervals 185
Chapter 19 Comparison of Means 197
Chapter 20 Comparison of Proportions 217
Chapter 21 Analysis of Survival Data 235
❘❙❚■ Contents
Clinical Trials: A Practical Guide ■❚❙❘
xi
Part IV: Special Trial Issues in Data Analysis
Chapter 22 Intention-to-Treat Analysis 255
Chapter 23 Subgroup Analysis 265
Chapter 24 Regression Analysis 273
Chapter 25 Adjustment for Covariates 287
Chapter 26 Confounding 295
Chapter 27 Interaction 305
Chapter 28 Repeated Measurements 317
Chapter 29 Multiplicity 329
Chapter 30 Missing Data 339
Chapter 31 Interim Monitoring and Stopping Rules 353
Part V: Reporting of Trials
Chapter 32 Overview of Reporting 365
Chapter 33 Trial Profile 377
Chapter 34 Presenting Baseline Data 385
Chapter 35 Use of Tables 391
Chapter 36 Use of Figures 407
Chapter 37 Critical Appraisal of a Report 427
Chapter 38 Meta-Analysis 439
Glossary 453
Abbreviations 461
Index 467