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Introduction to statistical methods for clinical trials / edited by Thomas D. Cook, David L. DeMets.

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Language:
English.
Publication date:
2008
Imprint:
Boca Raton, FL : Chapman & Hall/CRC, c2008.
Format:
  • Book
  • xxiii, 439 p. : ill. ; 25 cm.
Bibliography:
Includes bibliographical references (p. 405-426) and index.
Contents:
  • PREFACE Introduction to Clinical Trials History and Background Ethics of Clinical Research Types of Research Design and Types of Trials The Need for Clinical Trials The Randomization Principle Timing of a Clinical Trial Trial Organization Protocol and Manual of Operations Regulatory Issues Overview of the Book Defining the Question Statistical Framework Elements of Study Question Outcome or Response Measures The Surrogate Outcome Composite Outcomes Summary Problems Study Design Early Phase Trials Phase III/IV Trials Non-Inferiority Designs Screening, Prevention, and Therapeutic Designs Adaptive Designs Conclusions Problems Sample Size Sample Size versus Information A General Setup for Frequentist Designs Loss to Follow-up and Non-Adherence Survival Data Clustered Data Tests for Interaction Equivalence/Non-Inferiority Trials Other Considerations Problems Randomization The Role of Randomization Fixed Randomization Procedures Treatment- and Response-Adaptive Randomization Procedures Covariate-Adaptive Randomization Procedures Summary and Recommendations Problems Data Collection and Quality Control Planning for Collection of Clinical Trial Data Categories of Clinical Data Data Quality Control Conclusions Survival Analysis Background Estimation of Survival Distributions Comparison of Survival Distributions Regression Models Composite Outcomes Summary Problems Longitudinal Data A Clinical Longitudinal Data Example The Subject-Specific Model Two-Stage Estimation The Random-Effects, Subject-Specific Model The Population-Average (Marginal) Model Restricted Maximum Likelihood Estimation (REML) Standard Errors Testing Additional Levels of Clustering Generalized Estimating Equations for Non-Normal Data Missing Data Summary Quality of Life Defining QoL Types of QoL Assessments Selecting a QoL Instrument Developing a QoL Instrument Quality of Life Data Analysis of QoL Data Summary Data Monitoring and Interim Analysis Data and Safety Monitoring Examples The Repeated Testing Problem Group Sequential Tests Triangular Test Curtailment Procedures Inference Following Sequential Tests Discussion Problems Selected Issues in the Analysis Bias in the Analysis of Clinical Trial Data Choice of Analysis Population Missing Data Subgroup Analyses Multiple Testing Procedures Summary Problems Closeout and Reporting Closing out a Trial Reporting Trial Results Problems Appendix: Delta Method, Maximum Likelihood Theory, and Information Delta Method Asymptotic Theory for Likelihood-Based Inference Hypothesis Testing Computing the MLE Information Brownian Motion REFERENCES INDEX.
  • (source: Nielsen Book Data)
Publisher's Summary:
Clinical trials have taken a prominent role in the research and approval of new drugs. To conduct rigorous clinical studies, present and future biostatisticians need a good background in the design and analysis of data gleaned from those studies. This text provides a summary of statistical design, including cross-over designs, sample size estimation, sequential methods for interim analyses, survival analysis, and repeated measures. The authors also discuss a number of topics not addressed in other books on the subject, including the use of surrogate variables, meta-analysis, and longitudinal designs. Each chapter includes examples and exercises, and data sets are available for download from the Internet.
(source: Nielsen Book Data)
Contributor:
Cook, Thomas D.
DeMets, David L., 1944-
Series:
Chapman & Hall/CRC texts in statistical science series
Texts in statistical science.
Subjects:
ISBN:
9781584880271
1584880279

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