Statistical Design and Analysis of Clinical Trials (Record no. 29647)

MARC details
000 -LEADER
fixed length control field 02446nam a22002417a 4500
001 - CONTROL NUMBER
control field 20241105143403.0
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20241105143949.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
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010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number 20150617
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 978-1-4822-5050-3 (eBook - PDF)
040 ## - CATALOGING SOURCE
Transcribing agency ddc
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title English
100 ## - MAIN ENTRY--PERSONAL NAME
Fuller form of name Weichung Joe Shih
240 ## - UNIFORM TITLE
Uniform title Statistical Design and Analysis of Clinical Trials.
245 ## - TITLE STATEMENT
Title Statistical Design and Analysis of Clinical Trials
Remainder of title Principles and Methods.
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Boca Raton, FL 33487-2742 |
Name of publisher, distributor, etc. Taylor & Francis Group, LLC CRC |
Date of publication, distribution, etc. 2016.
300 ## - PHYSICAL DESCRIPTION
Extent 240 Pages
520 ## - SUMMARY, ETC.
Summary, etc. Statistical Design, Monitoring, and Analysis of Clinical Trials, Second Edition concentrates on the biostatistics component of clinical trials. This new edition is updated throughout and includes five new chapters.<br/><br/>Developed from the authors’ courses taught to public health and medical students, residents, and fellows during the past 20 years, the text shows how biostatistics in clinical trials is an integration of many fundamental scientific principles and statistical methods. The book begins with ethical and safety principles, core trial design concepts, the principles and methods of sample size and power calculation, and analysis of covariance and stratified analysis. It then focuses on sequential designs and methods for two-stage Phase II cancer trials to Phase III group sequential trials, covering monitoring safety, futility, and efficacy. The authors also discuss the development of sample size reestimation and adaptive group sequential procedures, phase 2/3 seamless design and trials with predictive biomarkers, exploit multiple testing procedures, and explain the concept of estimand, intercurrent events, and different missing data processes, and describe how to analyze incomplete data by proper multiple imputations.<br/><br/>This text reflects the academic research, commercial development, and public health aspects of clinical trials. It gives students and practitioners a multidisciplinary understanding of the concepts and techniques involved in designing, monitoring, and analyzing various types of trials. The book’s balanced set of homework assignments and in-class exercises are appropriate for students and researchers in (bio)statistics, epidemiology, medicine, pharmacy, and public health.
600 ## - SUBJECT ADDED ENTRY--PERSONAL NAME
General subdivision Biostatistics
700 ## - ADDED ENTRY--PERSONAL NAME
Fuller form of name Joseph Aisner
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme ddc
Koha item type E-BOOKS
Suppress in OPAC
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Date acquired Total checkouts Barcode Date last seen Copy number Price effective from Koha item type
          MWALIMU NYERERE LEARNING RESOURCES CENTRE-CUHAS BUGANDO MWALIMU NYERERE LEARNING RESOURCES CENTRE-CUHAS BUGANDO 11/05/2024   20241105143403.0 11/05/2024 20241105143403.0 11/05/2024 E-BOOKS
Catholic University of  Health and Allied Sciences - CUHAS
Directorate of ICT @ 2024