A Concise Guide to Clinical Trials
Allan Hackshaw(auth.)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
Chapter 1 Fundamental Concepts (pages 1–16):
Chapter 2 Types of Outcome Measures and Understanding them (pages 17–29):
Chapter 3 Design and Analysis of Phase I Trials (pages 31–38):
Chapter 4 Design and Analysis of Phase II Trials (pages 39–56):
Chapter 5 Design of Phase III Trials (pages 57–76):
Chapter 6 Randomisation (pages 77–89):
Chapter 7 Analysis and Interpretation of Phase III Trials (pages 91–128):
Chapter 8 Systematic Reviews and Meta?Analyses (pages 129–139):
Chapter 9 Health?Related Quality of Life and Health Economic Evaluation (pages 141–155):
Chapter 10 Setting Up, Conducting and Reporting Trials (pages 157–186):
Chapter 11 Regulations and Guidelines (pages 187–201):