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Christopher J. Bulpi Randomised Controlled Clinical Tria (Hardback) (UK IMPORT)

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Item specifics

Condition
Brand New: A new, unread, unused book in perfect condition with no missing or damaged pages. See the ...
Book Title
Randomised Controlled Clinical Trials
Publication Name
Randomised Controlled Clinical Trials
Title
Randomised Controlled Clinical Trials
Author
Christopher J. Bulpitt
Format
Hardcover
EAN
9780792342571
ISBN
9780792342571
Edition
2nd ed. 1996
Publisher
Springer
Genre
Computing & Internet
Topic
Law & Politics
Release Year
1996
Release Date
30/09/1996
Language
English
Country/Region of Manufacture
NL
Item Height
235mm
Item Length
9.3in
Publication Year
1996
Type
Textbook
Features
Revised
Item Width
6.1in
Item Weight
62.8 Oz
Number of Pages
IX, 437 Pages

About this product

Product Information

After 13 years there are new areas to discuss and more recent trials to be included. Good clinical practice; evaluation of quality of life; measurement of the benefit: risk comparison; determination of cost- effectiveness and cost utility; stopping rules for trials; meta-analysis and subgroup analysis are all new sections. The references are expanded from 305 to 512 and include the recent advances in trial design, such as the n -of-1 trials and megatrials, and up-to-date examples to illustrate the points made in the 20 chapters.

Product Identifiers

Publisher
Springer
ISBN-10
0792342577
ISBN-13
9780792342571
eBay Product ID (ePID)
213499

Product Key Features

Author
Christopher J. Bulpitt
Publication Name
Randomised Controlled Clinical Trials
Format
Hardcover
Language
English
Features
Revised
Publication Year
1996
Type
Textbook
Number of Pages
IX, 437 Pages

Dimensions

Item Length
9.3in
Item Width
6.1in
Item Weight
62.8 Oz

Additional Product Features

Number of Volumes
1 Vol.
Lc Classification Number
Rs400-431
Edition Description
Revised Edition
Edition Number
2
Table of Content
Preface. 1. Introduction. 2. The History of Controlled Trials. 3. Ethical Considerations. 4. The Objectives of a Randomised Controlled Trial. 5. Different Trial Designs. 6. How Many Subjects are Required for a Trial? 7. How to Ensure that the Results are Free of Bias. 8. Writing the Protocol. 9. Recruitment of Subjects. 10. Information to be Collected During a Trial. 11. The Conduct of the Trial - Good Clinical Practice. 12. Stopping Rules for Trials. 13. The Variability and Validity of Results. 14. Analysis of the Results, Subgroup and Meta-Analysis. 15. The Evaluation of Subjective Well-Being and Measurement of Quality of Life. 16. The Detection of Adverse Drug Reactions. 17. Measurement of the Benefit: Risk Comparison, Cost-Effectiveness and Cost-Utility. 18. Early Trials on New Drugs. 19. Failure to Accept the Results of Randomised Controlled Trials. 20. The Advantages and Disadvantages of Randomised Controlled Trials. References. Index.
Copyright Date
1996
Target Audience
Scholarly & Professional
Topic
Clinical Medicine, Medical Law & Legislation, Chemistry / Clinical, General
Lccn
96-041439
Dewey Decimal
615.5/0724
Dewey Edition
20
Illustrated
Yes
Genre
Law, Science, Medical

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