[PDF.90sh] Design and Analysis of Clinical Trials with Time-to-Event Endpoints (Chapman & Hall/CRC Biostatistics Series)

Design and Analysis of Clinical Trials with Time-to-Event Endpoints (Chapman & Hall/CRC Biostatistics Series)

[PDF.rh70] Design and Analysis of Clinical Trials with Time-to-Event Endpoints (Chapman & Hall/CRC Biostatistics Series)

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 | #4496645 in Books |  2009-04-23 | Original language:English | PDF # 1 |  9.10 x1.50 x6.50l,2.15 | File type: PDF | 616 pages

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||2 of 3 people found the following review helpful.| good text and reference on clinical trials with time-to-event endpoints|By Michael R. Chernick|Often in clinical trials particularly oncology trials time-to-event are the endpoints of primary interest. The endpoint could be time of death, time to remittance, time to recurrence or something else. In the recent RE-LY trial which was a stroke prevention trial the dual primary en

Using time-to-event analysis methodology requires careful definition of the event, censored observation, provision of adequate follow-up, number of events, and independence or "noninformativeness" of the censoring mechanisms relative to the event. Design and Analysis of Clinical Trials with Time-to-Event Endpoints provides a thorough presentation of the design, monitoring, analysis, and interpretation of clinical trials in which time-to-event is of cr...

You easily download any file type for your device.Design and Analysis of Clinical Trials with Time-to-Event Endpoints (Chapman & Hall/CRC Biostatistics Series)   |  From Chapman and Hall/CRC.Not only was the story interesting, engaging and relatable, it also teaches lessons.

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