Randomized Controlled Clinical Trials
Kluwer Academic Publishers (Verlag)
978-90-247-2749-0 (ISBN)
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When discussing a randomised controlled trial, it is neither practicable nor desirable to divorce theory from practice, however the first ten chapters con- centrate mainly on theory, and the remainder focus on practice. The segment on trial design is followed by sections on writing the protocol, designing the forms, conducting the trial, and analysing the results. This book is meant to serve both as a reference manual and a practical guide to the design and performance of a trial.
1. Introduction.- 2. The history of controlled trials.- 3. Ethical considerations.- 4. The objectives of a randomised controlled trial.- 5. Validity of the results.- 6. Recruitment of subjects.- 7. How to ensure that the control and treated patients are similar in all important respects.- 8. How to ensure that the results are free of bias.- 9. The variability of results.- 10. How many subjects are required for a trial?.- 11. Different trial designs.- 12. Writing the protocol.- 13. Information to be collected during a trial.- 14. The conduct of the trial.- 15. Analysis of the trial results.- 16. The evaluation of subjective well-being.- 17. Early trials on new drugs.- 18. The detection of adverse drug reactions.- 19. Failure to accept the results of randomised controlled trials.- 20. The advantages and disadvantages of randomised controlled trials.- 21. References.
Reihe/Serie | Developments in Biostatistics & Epidemiology ; 1 |
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Zusatzinfo | 4 black & white illustrations, biography |
Verlagsort | Dordrecht |
Sprache | englisch |
Maße | 130 x 190 mm |
Gewicht | 600 g |
Themenwelt | Studium ► Querschnittsbereiche ► Prävention / Gesundheitsförderung |
ISBN-10 | 90-247-2749-9 / 9024727499 |
ISBN-13 | 978-90-247-2749-0 / 9789024727490 |
Zustand | Neuware |
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