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      1. Medicin
      2. Medicin: allmänt
      3. Medicinsk utrustning och medicinska tekniker

      Clinical Trial Data Analysis Using R and SAS

      AvDing-Geng (Din) Chen,Karl E. Peace

      Inbunden, Engelska, 2017

      Del i serien Chapman & Hall/CRC Biostatistics Series

      2 129 kr

      Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

      Fler format och utgåvor

      Häftad

      809 kr

      Beskrivning

      Review of the First Edition"The goal of this book, as stated by the authors, is to fill the knowledge gap that exists between developed statistical methods and the applications of these methods. Overall, this book achieves the goal successfully and does a nice job. I would highly recommend it …The example-based approach is easy to follow and makes the book a very helpful desktop reference for many biostatistics methods."—Journal of Statistical SoftwareClinical Trial Data Analysis Using R and SAS, Second Edition provides a thorough presentation of biostatistical analyses of clinical trial data with step-by-step implementations using R and SAS. The book’s practical, detailed approach draws on the authors’ 30 years’ experience in biostatistical research and clinical development. The authors develop step-by-step analysis code using appropriate R packages and functions and SAS PROCS, which enables readers to gain an understanding of the analysis methods and R and SAS implementation so that they can use these two popular software packages to analyze their own clinical trial data.What’s New in the Second Edition Adds SAS programs along with the R programs for clinical trial data analysis. Updates all the statistical analysis with updated R packages. Includes correlated data analysis with multivariate analysis of variance. Applies R and SAS to clinical trial data from hypertension, duodenal ulcer, beta blockers, familial andenomatous polyposis, and breast cancer trials. Covers the biostatistical aspects of various clinical trials, including treatment comparisons, time-to-event endpoints, longitudinal clinical trials, and bioequivalence trials.

      Produktinformation

      • Utgivningsdatum:2017-05-03
      • Mått:156 x 234 x 27 mm
      • Vikt:520 g
      • Format:Inbunden
      • Språk:Engelska
      • Serie:Chapman & Hall/CRC Biostatistics Series
      • Antal sidor:378
      • Upplaga:2
      • Förlag:Taylor & Francis Inc
      • ISBN:9781498779524

      Utforska kategorier

      • Medicinsk utrustning och medicinska tekniker inom Medicin
      • Epidemiologi och medicinsk statistik inom Medicin
      • Matematisk statistik inom Naturvetenskap och teknik

      Mer om författaren

      Ding-Geng (Din) Chen, Ph.D., is a professor at the University of Rochester Medical Center. Dr. Chen has vast experience inbiostatistical research and clinical trial development and methodology. He has authored or co-authored more than 100 journalpublications on biostatistical methodologies and applications. He is also the co-author (with Dr. Peace) of Clinical Trial Methodologyand Clinical Trial Data Analysis Using R and a co-editor (with Drs. Sun and Peace) of Interval-Censored Time-to-Event Data: Methodsand Applications. He is a member of the American Statistical Association, chair for the STAT section of the American Public HealthAssociation, an associate editor of the Journal of Statistical Computation and Simulation, and an editorial board member of severalother journals.Karl E. Peace, Ph.D., is the Georgia Cancer Coalition Distinguished Cancer Scholar, senior research scientist, and professor ofbiostatistics in the Jiann-Ping Hsu College of Public Health at Georgia Southern University. He is also an adjunct professor ofbiostatistics at the VCU School of Medicine. Dr. Peace is a reviewer or editor of several journals, the founding editor of the Journal ofBiopharmaceutical Statistics, and a fellow of the American Statistical Association. He has authored or co-authored over 150 articlesand 10 books. He has received numerous awards, including the University System of Georgia Board of Regents’ Alumni Hall of FameAward, the First President’s Medal for outstanding contributions to Georgia Southern University, and distinguished meritorious serviceawards from the American Public Health Association and other organizations. In 2012, the American Statistical Association created theKarl E. Peace Award for Outstanding Statistical Contributions for the Betterment of Society.

      Recensioner i media

      " . . . this book provides a very useful overview of the statistical methods used in the analysis of clinical trials, along with their implementations. This will particularly help clinical practitioners to apply these methodologies in their own scientific problems . . . I would really like to thank the authors, D. Chen, K. E. Peace and P. Zhang, for such a nice readymade reference for clinical trial analysis, with very interesting real data illustrations."~Abhik Ghosh, International Society for Clinical Biostatistics

      Innehållsförteckning

      • Preface. Introduction to R. Overview of Clinical Trials. Sample Size Determination in Clinical Trials. Two Treatment Comparisons in Clinical Trials. Multi-Arm Comparisons in Clinical Trials (ANOVA). Treatment Comparisons Incorporating Covariates in Clinical Trials (ANCOVA). Clinical Trials with Time-to-Events Endpoints. Clinical Trials with Repeated Measures. Meta-Analysis in Clinical Trials. Bayesian Methods in Clinical Trials. Group Sequential Designs and Monitoring in Clinical Trials. Bioequivalence Clinical Trials. Monitoring Clinical Trials for Adverse Events.
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