Clinical Trials: Design, Conduct, and AnalysisOxford University Press, 1986 - 469 pages The definitive reference work on clinical trials, this book presents a wealth of detailed, practical information on the design, conduct, and analysis of both single center and multicenter trials. No other book on clinical trials offers as much detail as Meinert does on such issues as sample size calculation, stratification and randomization, data systems design, consent form development, publication policies, preparation of funding requests, and reporting procedures. |
From inside the book
Results 1-5 of 83
Page xvi
... Personnel 19.8 Questions concerning patient 21.5.2 Consultants follow - up 21.5.3 Equipment 19.9 Questions concerning the 21.5.4 Supplies outcome measure 21.5.5 Travel 19.10 Questions concerning data 21.5.6 Patient care costs integrity ...
... Personnel 19.8 Questions concerning patient 21.5.2 Consultants follow - up 21.5.3 Equipment 19.9 Questions concerning the 21.5.4 Supplies outcome measure 21.5.5 Travel 19.10 Questions concerning data 21.5.6 Patient care costs integrity ...
Page xvii
... personnel in 24.2 Publication questions unmasked trials 24.2.1 When to publish ? 22.6.2 Separation of personnel 24.2.2 Presentation or publication ? responsible for patient 24.2.3 Where to publish ? care and safety monitoring 24.2.4 ...
... personnel in 24.2 Publication questions unmasked trials 24.2.1 When to publish ? 22.6.2 Separation of personnel 24.2.2 Presentation or publication ? responsible for patient 24.2.3 Where to publish ? care and safety monitoring 24.2.4 ...
Page xxi
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Page 25
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Page 26
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Contents
A stateof | 1 |
223 | 12 |
The activities of | 18 |
Cost and related issues | 40 |
masked allocation | 90 |
Use of items from other | 119 |
Patient recruitment | 149 |
Patient followup | 185 |
randomization | 219 |
Essential management | 232 |
Preparation of | 264 |
Appendix H Budget summary | 279 |
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Common terms and phrases
Abstract summaries advisory-review allocation ratio Aspirin assess baseline Chapter clinical trial close-out consent control treatment Coronary Drug Project cost data center data collection data coordinating center data dredging data entry data forms database disease Drug Project Research Fisher's exact test follow-up visit funding Gallstone Group Diabetes Program Hypertension Institute investigators laboratory masked ment methods monitoring committee multicenter trials myocardial infarction NCGS needed niacin number of patients outcome measure p-value paper patient recruitment patients enrolled phenformin physician placebo procedures Program Research Group Project Research Group protocol publication Question randomization records responsible safety monitoring sample sample size schedule Section specified sponsor study treatments subgroups TEMC test treatment tients tion tolbutamide treat treatment allocation treatment assignment treatment effects monitoring treatment group treatment monitoring trial involving trials sketched UGDP University Group Diabetes variable Yes Yes Yes