A Concise Guide to Clinical Trials

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John Wiley & Sons, 2011年9月7日 - 224 頁
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Clinical trials have revolutionized the way disease is prevented, detected and treated, and early death avoided, and they continue to be an expanding area of research. They are central to the work of pharmaceutical companies, and there are many academic and public sector organizations that conduct trials on a wide variety of interventions, including drugs, devices, surgical techniques, and changes in behaviour and lifestyle.

A Concise Guide to Clinical Trials provides a comprehensive yet easy-to-read overview of the design, conduct and analysis of trials. It requires no prior knowledge on the subject as the important concepts are introduced throughout. There are chapters that distinguish between the different types of trials, and an introduction to systematic reviews, health-related quality of life and health economic evaluation. The book also covers the ethical and legal requirements in setting up a clinical trial due to an increase in governance responsibilities and regulations.

This practical guidebook is ideal for busy clinicians and other health professionals who do not have enough time to attend courses or search through extensive textbooks. It will help anyone involved in undertaking clinical research, or those reading about trials. The book is aimed at:

  • Those wishing to learn about clinical trials for the first time, or as a quick reference guide, for example as part of a taught course on clinical trials
  • Health professionals who wish to conduct their own trials, or participate in other people’s studies
  • People who work in pharmaceutical companies, grant funding organisations, or regulatory agencies
 

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內容

Preface
Types of outcome measures and understanding
Design and analysis of phase I trials
Design and analysis of phase II trials
Design of phase III trials
Randomisation
Analysis and interpretation of phase III trials
interpreting results
Systematic reviews and metaanalyses
Healthrelated quality of life and health economic
Setting up conducting and reporting trials
Regulations and guidelines
Reading list
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關於作者 (2011)

Allan Hackshaw
Deputy Director of the Cancer Research UK & UCL Cancer Trials Centre
Senior Lecturer in Epidemiology & Medical Statistics

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