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 85
Page xii
... schedule noncompliance 7.2.8 Treatment facilities and 9.3.10 Treatment lag time resources 9.3.11 Stratification for control of 7.2.9 Design and operating features baseline risk factors of the trial 9.3.12 Degree of type I and II error ...
... schedule noncompliance 7.2.8 Treatment facilities and 9.3.10 Treatment lag time resources 9.3.11 Stratification for control of 7.2.9 Design and operating features baseline risk factors of the trial 9.3.12 Degree of type I and II error ...
Page xiii
... schedule 9.5.2.1 Normal approximation for 10.5 Mechanics of masking treatment comparison of two assignments ... schedule for the calculation based on chi- Macular Photocoagulation square and inverse sine Study using pseudo- transform ...
... schedule 9.5.2.1 Normal approximation for 10.5 Mechanics of masking treatment comparison of two assignments ... schedule for the calculation based on chi- Macular Photocoagulation square and inverse sine Study using pseudo- transform ...
Page xiv
... schedule 12.6.5 Form color coding 12.6.6 Form assembly 12.6.7 Arrangement of items on 12.2.1 Introduction forms 12.2.2 Baseline clinic visit 12.6.8 Format schedule 12.6.8.1 Items designed for 12.2.3 Follow - up clinic visit schedule ...
... schedule 12.6.5 Form color coding 12.6.6 Form assembly 12.6.7 Arrangement of items on 12.2.1 Introduction forms 12.2.2 Baseline clinic visit 12.6.8 Format schedule 12.6.8.1 Items designed for 12.2.3 Follow - up clinic visit schedule ...
Page xxiii
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Page 13
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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