Sample Size Calculations in Clinical Research Sample Size Calculations in Clinical Research
Chapman & Hall/CRC Biostatistics Series

Sample Size Calculations in Clinical Research

    • USD 54.99
    • USD 54.99

Descripción editorial

Praise for the Second Edition:

"… this is a useful, comprehensive compendium of almost every possible sample size formula. The strong organization and carefully defined formulae will aid any researcher designing a study." -Biometrics

"This impressive book contains formulae for computing sample size in a wide range of settings. One-sample studies and two-sample comparisons for quantitative, binary, and time-to-event outcomes are covered comprehensively, with separate sample size formulae for testing equality, non-inferiority, and equivalence. Many less familiar topics are also covered …" – Journal of the Royal Statistical Society

Sample Size Calculations in Clinical Research, Third Edition presents statistical procedures for performing sample size calculations during various phases of clinical research and development. A comprehensive and unified presentation of statistical concepts and practical applications, this book includes a well-balanced summary of current and emerging clinical issues, regulatory requirements, and recently developed statistical methodologies for sample size calculation.

Features:
Compares the relative merits and disadvantages of statistical methods for sample size calculations Explains how the formulae and procedures for sample size calculations can be used in a variety of clinical research and development stages Presents real-world examples from several therapeutic areas, including cardiovascular medicine, the central nervous system, anti-infective medicine, oncology, and women’s health Provides sample size calculations for dose response studies, microarray studies, and Bayesian approaches
This new edition is updated throughout, includes many new sections, and five new chapters on emerging topics: two stage seamless adaptive designs, cluster randomized trial design, zero-inflated Poisson distribution, clinical trials with extremely low incidence rates, and clinical trial simulation.

GÉNERO
Ciencia y naturaleza
PUBLICADO
2017
15 de agosto
IDIOMA
EN
Inglés
EXTENSIÓN
510
Páginas
EDITORIAL
CRC Press
VENDEDOR
Taylor & Francis Group
TAMAÑO
23.1
MB
Biosimilars Biosimilars
2013
Design and Analysis of Animal Studies in Pharmaceutical Development Design and Analysis of Animal Studies in Pharmaceutical Development
1998
Controversial Statistical Issues in Clinical Trials Controversial Statistical Issues in Clinical Trials
2016
Encyclopedia of Biopharmaceutical Statistics - Four Volume Set Encyclopedia of Biopharmaceutical Statistics - Four Volume Set
2018
Statistics in Drug Research Statistics in Drug Research
2002
Statistical Design and Analysis in Pharmaceutical Science Statistical Design and Analysis in Pharmaceutical Science
2018
Advanced Statistical Analytics for Health Data Science with SAS and R Advanced Statistical Analytics for Health Data Science with SAS and R
2025
R for Health Technology Assessment R for Health Technology Assessment
2025
Design and Analysis of Clinical Trials with Time-to-Event Endpoints Design and Analysis of Clinical Trials with Time-to-Event Endpoints
2009
Generalized Linear Models Generalized Linear Models
2000
Statistics In the Pharmaceutical Industry Statistics In the Pharmaceutical Industry
2019
Design and Analysis of Animal Studies in Pharmaceutical Development Design and Analysis of Animal Studies in Pharmaceutical Development
1998