9783319220048 - sample size determination in clinical trials with multiple endpoints (springerbriefs in statistics) de sozu, takashi; sugimoto, tomoyuki; hamasaki, toshimitsu; evans, scott r. (15 resultados)

Sample Size Determination in Clinical Trials With Multiple Endpoints
Sozu, Takashi; Sugimoto, Tomoyuki; Hamasaki, Toshimitsu; Evans, Scott R.
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Sample Size Determination in Clinical Trials with Multiple Endpoints (SpringerBriefs in Statistics)
Sozu, Takashi; Sugimoto, Tomoyuki; Hamasaki, Toshimitsu; Evans, Scott R.
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Sample Size Determination in Clinical Trials with Multiple Endpoints (SpringerBriefs in Statistics)
Sozu, Takashi; Sugimoto, Tomoyuki; Hamasaki, Toshimitsu; Evans, Scott R.
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Taschenbuch. Condición: Neu. Druck auf Anfrage Neuware - Printed after ordering - 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 brie y examines trials designed with an alternative hypothesis of an effect on AT LEAST ONE endpoint with a prespecified non-ordering of endpoints.

Sample Size Determination in Clinical Trials With Multiple Endpoints
Sozu, Takashi/ Sugimoto, Tomoyuki/ Hamasaki, Toshimitsu/ Evans, Scott R.
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Librería: Revaluation Books, Exeter, , Reino UnidoRevaluation Books
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Taschenbuch. Condición: Neu. Sample Size Determination in Clinical Trials with Multiple Endpoints | Takashi Sozu (u. a.) | Taschenbuch | SpringerBriefs in Statistics | vi | Englisch | 2015 | Springer | EAN 9783319220048 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]ha…rtmann[at]springer[dot]com | Anbieter: preigu.

Sample Size Determination in Clinical Trials with Multiple Endpoints (SpringerBriefs in Statistics)
Sozu, Takashi, Sugimoto, Tomoyuki, Hamasaki, Toshimitsu, Eva
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Sample Size Determination in Clinical Trials With Multiple Endpoints
Sozu, Takashi; Sugimoto, Tomoyuki; Hamasaki, Toshimitsu; Evans, Scott R.
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Librería: GreatBookPrices, Columbia, MD, Estados Unidos de AmericaGreatBookPrices
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Librería: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, , AlemaniaBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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 statistic…ians 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 brie y examines trials designed with an alternative hypothesis of an effect on AT LEAST ONE endpoint with a prespecified non-ordering of endpoints. 104 pp. Englisch.

Sample Size Determination in Clinical Trials with Multiple Endpoints
Takashi Sozu|Tomoyuki Sugimoto|Toshimitsu Hamasaki|Scott R. Evans
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Librería: moluna, Greven, , Alemaniamoluna
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Condición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Reviews statistical issues in clinical trials with multiple endpointsDescribes methods for power and sample size calculations in clinical trials with multiple endpoints including recently developed approaches not cove…red in other booksInclu.

Sample Size Determination in Clinical Trials with Multiple Endpoints (SpringerBriefs in Statistics)
Sozu, Takashi; Sugimoto, Tomoyuki; Hamasaki, Toshimitsu; Evans, Scott R.
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Librería: Majestic Books, Hounslow, , Reino UnidoMajestic Books
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Condición: New. Print on Demand pp. 95.

Sample Size Determination in Clinical Trials with Multiple Endpoints (SpringerBriefs in Statistics)
Sozu, Takashi; Sugimoto, Tomoyuki; Hamasaki, Toshimitsu; Evans, Scott R.
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Librería: Biblios, frankfurt am main, HESSE, AlemaniaBiblios
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Condición: New. PRINT ON DEMAND pp. 95.

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Librería: buchversandmimpf2000, Emtmannsberg, BAYE, Alemaniabuchversandmimpf2000
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Taschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -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 brie¿y examines trials designed with an alternative hypothesis of an effect on AT LEAST ONE endpoint with a prespeci¿ed non-ordering of endpoints.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 104 pp. Englisch.