PDF Ebook Clinical Trials: A Methodologic Perspective (Wiley Series in Probability and Statistics)
- February 20, 2017
- By Lorsika
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PDF Ebook Clinical Trials: A Methodologic Perspective (Wiley Series in Probability and Statistics)
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Clinical Trials: A Methodologic Perspective (Wiley Series in Probability and Statistics)
PDF Ebook Clinical Trials: A Methodologic Perspective (Wiley Series in Probability and Statistics)
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From the Back Cover
Presents elements of clinical trial methods that are essential in planning, designing, conducting, analyzing, and interpreting clinical trials with the goal of improving the evidence derived from these important studies This Third Edition builds on the text's reputation as a straightforward, detailed, and authoritative presentation of quantitative methods for clinical trials. Readers will encounter the principles of design for various types of clinical trials, and are then skillfully guided through the complete process of planning the experiment, assembling a study cohort, assessing data, and reporting results. Throughout the process, the author alerts readers to problems that may arise during the course of the trial and provides common sense solutions. All stages of therapeutic development are discussed in detail, and the methods are not restricted to a single clinical application area. The author bases current revisions and updates on his own experience, classroom instruction, and feedback from teachers and medical and statistical professionals involved in clinical trials. The Third Edition greatly expands its coverage, ranging from statistical principles to new and provocative topics, including alternative medicine and ethics, middle development, comparative studies, and adaptive designs. At the same time, it offers more pragmatic advice for issues such as selecting outcomes, sample size, analysis, reporting, and handling allegations of misconduct. Readers familiar with the First and Second Editions will discover revamped exercise sets, an updated and extensive reference section, new material on endpoints and the developmental pipeline, among others, and revisions of numerous sections. In addition, this book: Features accessible and broad coverage of statistical design methods—the crucial building blocks of clinical trials and medical research—now complete with new chapters on overall development, middle development, comparative studies, and adaptive designs Teaches readers to design clinical trials that produce valid qualitative results backed by rigorous statistical methods Contains an introduction and summary in each chapter to reinforce key points Includes discussion questions to stimulate critical thinking and help readers understand how they can apply their newfound knowledge Provides extensive references to direct readers to the most recent literature Includes numerous new or revised exercises throughout Clinical Trials: A Methodologic Perspective, Third Edition is a textbook accessible to advanced undergraduate students in the quantitative sciences, graduate students in public health and the life sciences, physicians training in clinical research methods, and biostatisticians and epidemiologists.
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About the Author
Steven Piantadosi, MD, PhD, is the Phase One Foundation Distinguished Chair and Director of the Samuel Oschin Cancer Institute, and Professor of Medicine at Cedars-Sinai Medical Center in Los Angeles, California. Dr. Piantadosi is one of the world's leading experts in the design and analysis of clinical trials for cancer research. He has taught clinical trial methods extensively in formal courses and short venues. He has advised numerous academic programs and collaborations nationally regarding clinical trial design and conduct, and has served on external advisory boards for the National Institutes of Health and other prominent cancer programs and centers. The author of more than 260 peer-reviewed scientific articles, Dr. Piantadosi has published extensively on research results, clinical applications, and trial methodology. While his papers have contributed to many areas of oncology, he has also collaborated on diverse studies outside oncology including lung disease and degenerative neurological disease.
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Product details
Series: Wiley Series in Probability and Statistics
Hardcover: 920 pages
Publisher: Wiley; 3 edition (August 28, 2017)
Language: English
ISBN-10: 1118959205
ISBN-13: 978-1118959206
Product Dimensions:
7 x 2 x 10.2 inches
Shipping Weight: 4 pounds (View shipping rates and policies)
Average Customer Review:
4.4 out of 5 stars
8 customer reviews
Amazon Best Sellers Rank:
#178,563 in Books (See Top 100 in Books)
It is a very good course book for graduates in clinical trial design and practice. It is also a great reference for biostatisticians and clinical investigators who have solid knowledge background in biostatistics and mathematics. However, it may be a challenge to understand the detailed statistic and math equations and theories by those clinical scientists in pharmacology, toxicology, PKDM, and even clinical data programmers and project managers in pharmaceutical industry. Since clinical trials in pharmaceutical industry are carried out following FDA and ICH guidelines, those clinical scientists and project managers may expect more practical procedures in clinical trial design and examples of data analyses and statistical decisions for new drugs or decease treatments, which demonstrate how to design and judge clinical trials under FDA and ICH guidelines.
Ok textbook but useful reference for any graduate math or stat person.
This is an excellent and thorough overview of clinical trial medicine.
A must have for those designing clinical studies. The section on approaches to early development are outstanding. Understandable to moderately statistically literates.
An incredibly thorough text!
This is an excellent book. It outlines the important issues of clinical trials well. It is understandable and thorough. A must for anyone who is interested in actually doing trials. Not a good book for a brief, superficial overview.
This book is very unique. Basic statistical concepts are clearly presented but only those concepts that are important in clinical trials. The author presents all the issues with clinical trials including ethical issues with some historical perspective. Principles of randomization and statistical design are clearly presented. It offers discussion of Bayesian techniques and meta-analyses, cross-over designs and group sequential methods (interim analyses). For statisticians doing clinical research like myself, this is a valuable reference source.
The amount of knowledge and the scope of this book are the exact need for the first contact with clinical trials. Yet, it is not a simple or superficial text. Instead, it not only will guide the reader through the basics of trials (and there is so much that is not basic in it) but the author points the reader to hundreds of papers and books that are landmarks. I regard this book itself as one of these landmarks!
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