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Sample size determination in clinical trials with multiple endpoints[electronic resource] /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
杜威分類號:	615.50724
書名/作者:	Sample size determination in clinical trials with multiple endpoints/ by Takashi Sozu ... [et al.].
其他作者:	Sozu, Takashi.
出版者:	Cham : : Springer International Publishing :, 2015.
面頁冊數:	vi, 95 p. : : ill., digital ;; 24 cm.
Contained By:	Springer eBooks
標題:	Clinical trials - Statistical methods.
標題:	Mathematical statistics.
標題:	Statistics.
標題:	Statistical Theory and Methods.
標題:	Statistics for Life Sciences, Medicine, Health Sciences.
標題:	Biostatistics.
ISBN:	9783319220055
ISBN:	9783319220048
內容註:	1.Introduction -- 2.Continuous Co-primary Endpoints -- 3.Binary Co-primary Endpoints -- 4.Convenient Sample Size Formula -- 5.Continuous Primary Endpoints -- 6. Further Developments -- A.Sample Size Calculation Using other Contrasts for Binary Endpoints -- B.Empirical Power for Sample Size Calculation for Binary Co-primary Endpoints -- C.Numerical Tables for Ck in the Convenient Sample Size Formula for the Three Co-primary Continuous Endpoints Cace -- D.Software Programs for Sample Size Calculation for Continuous Co-primary Endpoints -- References.
摘要、提要註:	This book integrates recent methodological developments for calculating the sample size and power in trials with more than one endpoint considered as multiple primary or co-primary, offering an important reference work for statisticians working in this area. The determination of sample size and the evaluation of power are fundamental and critical elements in the design of clinical trials. If the sample size is too small, important effects may go unnoticed; if the sample size is too large, it represents a waste of resources and unethically puts more participants at risk than necessary. Recently many clinical trials have been designed with more than one endpoint considered as multiple primary or co-primary, creating a need for new approaches to the design and analysis of these clinical trials. The book focuses on the evaluation of power and sample size determination when comparing the effects of two interventions in superiority clinical trials with multiple endpoints. Methods for sample size calculation in clinical trials where the alternative hypothesis is that there are effects on ALL endpoints are discussed in detail. The book also brieﬂy examines trials designed with an alternative hypothesis of an effect on AT LEAST ONE endpoint with a prespeciﬁed non-ordering of endpoints.
電子資源:	http://dx.doi.org/10.1007/978-3-319-22005-5

Sample size determination in clinical trials with multiple endpoints[electronic resource] /
Sample size determination in clinical trials with multiple endpoints[electronic resource] /by Takashi Sozu ... [et al.]. - Cham :Springer International Publishing :2015. - vi, 95 p. :ill., digital ;24 cm. - SpringerBriefs in statistics,2191-544X. - SpringerBriefs in statistics..

1.Introduction -- 2.Continuous Co-primary Endpoints -- 3.Binary Co-primary Endpoints -- 4.Convenient Sample Size Formula -- 5.Continuous Primary Endpoints -- 6. Further Developments -- A.Sample Size Calculation Using other Contrasts for Binary Endpoints -- B.Empirical Power for Sample Size Calculation for Binary Co-primary Endpoints -- C.Numerical Tables for Ck in the Convenient Sample Size Formula for the Three Co-primary Continuous Endpoints Cace -- D.Software Programs for Sample Size Calculation for Continuous Co-primary Endpoints -- References.

This book integrates recent methodological developments for calculating the sample size and power in trials with more than one endpoint considered as multiple primary or co-primary, offering an important reference work for statisticians working in this area. The determination of sample size and the evaluation of power are fundamental and critical elements in the design of clinical trials. If the sample size is too small, important effects may go unnoticed; if the sample size is too large, it represents a waste of resources and unethically puts more participants at risk than necessary. Recently many clinical trials have been designed with more than one endpoint considered as multiple primary or co-primary, creating a need for new approaches to the design and analysis of these clinical trials. The book focuses on the evaluation of power and sample size determination when comparing the effects of two interventions in superiority clinical trials with multiple endpoints. Methods for sample size calculation in clinical trials where the alternative hypothesis is that there are effects on ALL endpoints are discussed in detail. The book also brieﬂy examines trials designed with an alternative hypothesis of an effect on AT LEAST ONE endpoint with a prespeciﬁed non-ordering of endpoints.

ISBN: 9783319220055

Standard No.: 10.1007/978-3-319-22005-5doiSubjects--Topical Terms:

467884
Clinical trials
--Statistical methods.

LC Class. No.: R853.C55

Dewey Class. No.: 615.50724

Sample size determination in clinical trials with multiple endpoints[electronic resource] /
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520 $a This book integrates recent methodological developments for calculating the sample size and power in trials with more than one endpoint considered as multiple primary or co-primary, offering an important reference work for statisticians working in this area. The determination of sample size and the evaluation of power are fundamental and critical elements in the design of clinical trials. If the sample size is too small, important effects may go unnoticed; if the sample size is too large, it represents a waste of resources and unethically puts more participants at risk than necessary. Recently many clinical trials have been designed with more than one endpoint considered as multiple primary or co-primary, creating a need for new approaches to the design and analysis of these clinical trials. The book focuses on the evaluation of power and sample size determination when comparing the effects of two interventions in superiority clinical trials with multiple endpoints. Methods for sample size calculation in clinical trials where the alternative hypothesis is that there are effects on ALL endpoints are discussed in detail. The book also brieﬂy examines trials designed with an alternative hypothesis of an effect on AT LEAST ONE endpoint with a prespeciﬁed non-ordering of endpoints.
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