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A Concise Guide to Clinical Trials Paperback – 17 Apr 2009


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Product details

  • Paperback: 226 pages
  • Publisher: John Wiley & Sons; 1 edition (17 April 2009)
  • Language: English
  • ISBN-10: 1405167742
  • ISBN-13: 978-1405167741
  • Product Dimensions: 15.3 x 1.3 x 23.1 cm
  • Average Customer Review: 5.0 out of 5 stars  See all reviews (1 customer review)
  • Amazon Bestsellers Rank: 488,489 in Books (See Top 100 in Books)
  • See Complete Table of Contents

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Product Description

Review

"This book will be of interest to clinicians who carry out their own trials or become part of multi centre trials. It is an excellent reference guide and provides good background reading material for courses on clinical trials." (Journal of Tropical Pediatrics, 2011)

"Well illustrated and peppered with illustrative examples for each topic; this is a practical and useful book that achieves its objectives. It is to be recommended." (ChemMedChem, 2010)

From the Back Cover

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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5 of 6 people found the following review helpful By M. Hughes on 6 Aug. 2009
Format: Paperback
This type of book is rare - a very easy-to-understand book explaining the different phases of clinical trials, the different forms of statistical analysis involved, and many practical tips and asides along the way on how to conduct trials. The author has a clear understanding of his audience - primarily physicians, nurses and other healthcare professionals wanting to get involved in experimental research - and unlike many others strikes a good balance that leaves the reader informed and unbaffled. Although not suitable for those who already have a sound and comprehensive knowledge of clinical tries, I recommend it for any healthcare professional who wants to progress their career or satisfy their intellectual curiosity by doing experimental research.
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Most Helpful Customer Reviews on Amazon.com (beta)

Amazon.com: 2 reviews
7 of 7 people found the following review helpful
Getting started with your clinical trial 12 Aug. 2009
By David Teira Serrano - Published on Amazon.com
Format: Paperback
When clinical trials are published in scientific journals, the authors should disclose their potential conflicts of interests. Here is mine: to my great benefit, I attended one of the courses organized by Allan Hackshaw at the Graduate School of University College London in order to provide a four-day introduction to clinical trials. I was surprised to discover how many students needed to conduct one of these for their doctoral dissertations, with just an elementary understanding of what a clinical trial is. Hackshaw's concise guide achieves two goals: it shows how complex clinical trials can be and yet provides clues to solve many of the difficulties you will probably find.

This is not a textbook, but a field guide: Hackshaw presents what practitioners do in a trial, stage by stage. The theory is kept to a minimum and is presented through examples, often drawn from real trials. If you do not have time to take a thorough course in statistics, you will find here the quickest possible introduction to the main concepts used in real medical publications. This concise guide will show you what you need to know in order to conduct your own trial: you will see the forest, so you can decide what you need to learn in order to conduct your own trial. At every stage, the author illustrates the choices you will have to make. Once you identify your potential dilemmas, you will probably need additional readings to design and interpret your trial and Hackshaw provides many useful suggestions in the references. One outstanding feature of this book is that it provides a really updated, hands-on, overview of the practical implications involved in the conduction of a trial today (organization, regulations, etc)

Since this is a field guide, the concepts are presented as they appear in the different stages of a trial. This may require going back and forth between chapters to grasp some of the more complicated statistical ideas. A glossary would have made things simpler, but there is a detailed index instead. All in all, I think you will be grateful to this book, because it gets you started.
Five Stars 10 Aug. 2014
By Vinh D Le - Published on Amazon.com
Format: Paperback Verified Purchase
Fast delivery - Great Book
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