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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