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ClinicalTrials2

Interpreting and Reporting Clinical Trials. A guide to the consort statement and the principles of randomised controlled trials

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Product Description

FOR INSTITUTIONS OUTSIDE AUSTRALIA

If you wish to order large numbers of this title for institutional and/or teaching purposes
please click here to complete a bulk order request form. We will then contact you
as soon as possible regarding price and postage options.


Discounts apply for volume sales of more than 10 copies, Please phone AMPCo book sales on +612 9562 6666 for a quote for discount price and postage, or email emjashop@ampco.com.au.

Essential guide for all those involved in the planning, conduct and interpretation of clinical research.


Edited by Anthony Keech, Val Gebski and Rhana Pike of the NHMRC Clinical Trials Centre in Sydney, this book explains and expands upon each of the items in the CONSORT checklist to elucidate how best to undertake and learn from clinical trials.


Highly recommended.


Contents


• Randomised controlled trials: elements of a good study


• Introducing the report of a randomised controlled trial: the title, abstract, scientific background and rationale


• Selecting participants for clinical trials


• Specifying interventions in a clinical trial


• Specifying objectives and outcomes for clinical trials


• Determining the sample size in a clinical trial


• Managing the resource demands of a large sample size in clinical trials: can you succeed with fewer subjects?


• Randomisation in clinical trials


• Allocation concealment and blinding: when ignorance is bliss


• Statistical methods in clinical trials


• Flow of participants in randomised studies


• Recruitment to randomised studies


• Baseline data in clinical trials


• Inclusion of patients in clinical trial analysis: the intention-to-treat principle


• Making sense of trial results: outcomes and estimation


• Subgroup analysis in clinical trials


• Applying subgroup analysis to individual patient decisions


• Multiple analyses in clinical trials: sound science or data dredging?


• Balancing the outcomes: reporting harms (adverse events)


• Interpreting the results of a clinical trial


• Generalising the results of trials to clinical practice


• Putting results of a clinical trial into perspective

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Additional Information

Weight 0.58 kg
Dimensions 28 x 22 x 5 cm
ISBN

9780977578641

Author

Anthony Keech, Val J. Gebski and Rhana Pike

Published Date

2007

Pages

166

Cover

soft cover

Publisher

MJAbooks

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