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| Available: Yes* |
| This title does not qualify for any discount. |
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| Edition: | 1st |
| Publisher: | Springer Nature |
| ISBN: | 0-387-30107-0 (0387301070) |
| ISBN-13: | 978-0-387-30107-5 (9780387301075) |
| Binding: | E E Book + ProQuest Ebook Central |
| Copyright: | 2006 |
| Publish Date: | 10/05 |
| Weight: | 0.00 Lbs. |
| Subject Class: | SCI (Medical Science and Research) |
| Return Policy: | Non-Returnable. |
| Table Of Contents: |
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| Discipline: | Medical Prof | | Subject Definition: | Clinical Trials; Data Collection-Methods | | NLM Class: | W 20.5 | | LC Class: | R853 | | Abstract: | This book will be useful to anyone serving on a data and safety monitoring board, or planning to do so, for colleagues in academia, industry and governmental agencies, and for teaching students in biostatistics, epidemiology, clinical trials and medical ethics. No other text has as extensive a collection of cases which provide insight into the many issues, often conflicting, that must be examined before recommendations to continue or discontinue a trial can be made. While depth in statistical methods is not required, some familiarity with statistical design and analysis issues in clinical trials is helpful. The cases cover trials which were terminated early for convincing evidence of benefit, or for harmful effects. Cases with complex issues are also included. This series of cases should provide broad background information for potential monitoring committee members and better prepare them for the challenges that may exist in the trials for which they are responsible. |
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