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Titlebook: Data Monitoring in Clinical Trials; A Case Studies Appro David L. DeMets,Curt D. Furberg,Lawrence M. Friedm Book 2006 Springer-Verlag New Y

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發(fā)表于 2025-3-23 13:08:34 | 只看該作者
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發(fā)表于 2025-3-23 13:58:27 | 只看該作者
Breaking New Ground: Data Monitoring in the Coronary Drug Projectmplex process. It may involve, among other things, the need to (1) determine whether the observed treatment differences are likely to represent real effects and are not due to chance; (2) weigh the importance of different response variables, some possibly trending in favor of the treatment and some
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發(fā)表于 2025-3-23 22:01:07 | 只看該作者
The Data Monitoring Experience in the Cardiac Arrhythmia Suppression Trial: The Need to Be Prepared s with a recent myocardial infarction would reduce the incidence of sudden death and total mortality, using three drugs known to suppress cardiac arrhythmias. Patients were randomized to receive either active drug or a matching placebo. The trial was terminated after only 15% of the planned-for even
14#
發(fā)表于 2025-3-23 23:50:48 | 只看該作者
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發(fā)表于 2025-3-24 03:08:49 | 只看該作者
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發(fā)表于 2025-3-24 06:38:17 | 只看該作者
Richard Lai,Ajin Jirachiefpattanaetic retinopathy. Benefit was detected early, but there where concerns about the possibility of late adverse effects. Calculations using projected blindness and death rates reassured the data monitoring committee that even large late adverse affects would not offset the early benefit already observed.
17#
發(fā)表于 2025-3-24 13:05:58 | 只看該作者
https://doi.org/10.1007/0-387-30107-0Division; Host; LDA; Statistica; complexity; design; eXist; evaluation; form; monitor; monitoring; object; repor
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發(fā)表于 2025-3-24 18:50:08 | 只看該作者
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