Cleophas / Zwinderman | Statistics Applied to Clinical Trials | E-Book | sack.de
E-Book

E-Book, Englisch, 562 Seiten, Web PDF

Reihe: Mathematics and Statistics

Cleophas / Zwinderman Statistics Applied to Clinical Trials


Fourth Auflage 2009
ISBN: 978-1-4020-9523-8
Verlag: Springer Netherland
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 562 Seiten, Web PDF

Reihe: Mathematics and Statistics

ISBN: 978-1-4020-9523-8
Verlag: Springer Netherland
Format: PDF
Kopierschutz: 1 - PDF Watermark



In 1948 the first randomized controlled trial was published by the English Medical Research Council in the British Medical Journal. Until then, observations had been uncontrolled. The intervening decades have seen significant improvement in the accuracy of trials. Today, clinical trial protocols are now routinely scrutinized by ethics committees, institutional and federal review boards, national and international scientific organizations, and monitoring committees charged with conducting interim analyses. The updated Third Edition of Statistics Applied to Clinical Trials explains classical statistical analyses of clinical trials, but equivalence testing, interim analyses, sequential analyses, meta-analyses, and provides a framework of the best statistical methods currently available for such purposes.

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Zielgruppe


Research

Weitere Infos & Material


Hypotheses, Data, Stratification.- The Analysis Of Efficacy Data.- The Analysis of Safety Data.- Log Likelihood Ratio Tests For Safety Data Analysis.- Equivalence Testing.- Statistical Power And Sample Size.- Interim Analyses.- Controlling The Risk of False Positive Clinical Trials.- Multiple Statistical Inferences.- The Interpretation of The P-Values.- Research Data Closer To Expectation Than Compatible With Random Sampling.- Statistical Tables For Testing Data Closer To Expectation Than Compatible With Random Sampling.- Principles Of Linear Regression.- Subgroup Analysis Using Multiple Linear Regression: Confounding, Interaction, Synergism.- Curvilinear Regression.- Logistic and Cox Regression, Markow Models, Laplace Transformations.- Regression Modeling for Improved Precision.- Post-Hoc Analyses in Clinical Trials, a Case for Logistic Regression Analysis.- Confounding.- Interaction.- Meta-Analysis, Basic Approach.- Meta-Analysis, Review and Update of Methodologies.- Crossover Studies with Continuous Variables.- Crossover Studies with Binary Responses.- Cross-Over Trials Should not be Used to Test Treatments with Different Chemical Class.- Quality-of-Life Assessments in Clinical Trials.- Statistical Analysis of Genetic Data.- Relationship Among Statistical Distributions.- Testing Clinical Trials for Randomness.- Clinical Trials do not Use Random Samples Anymore.- Clinical Data Where Variability is More Important than Averages.- Testing Reproducibility.- Validating Qualitative Diagnostic Tests.- Uncertainty of Qualitative Diagnostic Tests.- Meta-Analysis of Diagnostic Accuracy.- Validating Quantitative Diagnostic Tests.- Summary of Validation Procedures for Diagnostic Tests.- Validating Surrogate Endpoints of Clinical Trials.- Methods for Repeated Measures Analysis.- Advanced Analysis of Variance, Random Effects and Mixed Effects Models.- Monte Carlo Methods.- Physicians’ Daily Life and the Scientific Method.- Clinical Trials: Superiority-Testing.- Trend-Testing.-Odds Ratios and Multiple Regression Models, Why and How to Use Them.- Statistics is no “Bloodless” Algebra.- Bias Due to Conflicts of Interests, Some Guidelines.



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