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 86
Page xiii
... randomization 10.3 Fixed randomization 10.3.1 Allocation ratio 10.3.2 Stratification 10.3.3 Block size 10.4 Construction of the randomization schedule 9.5.2.1 Normal approximation for 10.5 Mechanics of masking treatment comparison of ...
... randomization 10.3 Fixed randomization 10.3.1 Allocation ratio 10.3.2 Stratification 10.3.3 Block size 10.4 Construction of the randomization schedule 9.5.2.1 Normal approximation for 10.5 Mechanics of masking treatment comparison of ...
Page xv
... Randomization and initiation of treatment 17.6 Filing and storing the original study records 14.8 Zelen consent procedure 17.7 Preparation of analysis tapes Chapter 15. Patient follow - up , closeout , and post - trial follow - up ...
... Randomization and initiation of treatment 17.6 Filing and storing the original study records 14.8 Zelen consent procedure 17.7 Preparation of analysis tapes Chapter 15. Patient follow - up , closeout , and post - trial follow - up ...
Page xvi
... randomization deciding whether or not to 19.5 Questions concerning masking respond 19.6 Questions concerning the 21.3.3 The response comparability of the 21.4 The study budget 21.4.1 Grants treatment groups 21.4.2 Contracts 19.7 ...
... randomization deciding whether or not to 19.5 Questions concerning masking respond 19.6 Questions concerning the 21.3.3 The response comparability of the 21.4 The study budget 21.4.1 Grants treatment groups 21.4.2 Contracts 19.7 ...
Page xxiii
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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