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A concise guide to clinical trials
A concise guide to clinical trials
Autore Hackshaw Allan K
Edizione [1st ed.]
Pubbl/distr/stampa Oxford, : Wiley-Blackwell, c2009
Descrizione fisica 1 online resource (225 p.)
Disciplina 615.19
615.50724
Soggetto topico Clinical trials
Clinical medicine - Research
ISBN 1-4443-5666-6
1-282-13959-2
9786612139598
1-4443-1172-7
1-4443-1171-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto A Concise Guide to Clinical Trials; Contents; Preface; Foreword; 1 Fundamental concepts; 2 Types of outcome measures and understanding them; 3 Design and analysis of phase I trials; 4 Design and analysis of phase II trials; 5 Design of phase III trials; 6 Randomisation; 7 Analysis and interpretation of phase III trials; 8 Systematic reviews and meta-analyses; 9 Health-related quality of life and health economic evaluation; 10 Setting up, conducting and reporting trials; 11 Regulations and guidelines; Reading list; Statistical formulae for calculating some 95% confidence intervals; Index
Record Nr. UNINA-9910826813103321
Hackshaw Allan K  
Oxford, : Wiley-Blackwell, c2009
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Contemporary clinical trials
Contemporary clinical trials
Pubbl/distr/stampa [New York], : Elsevier, ©2005-
Disciplina 616
Soggetto topico Clinical trials
Clinical trials as Topic - methods
Research Design
Études cliniques
Étude clinique
Soggetto genere / forma Periodical
Periodicals.
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
Soggetto non controllato Medical Research
ISSN 1559-2030
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Contemp clin trials 4
Record Nr. UNINA-9910146158303321
[New York], : Elsevier, ©2005-
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Contemporary clinical trials
Contemporary clinical trials
Pubbl/distr/stampa [New York], : Elsevier, ©2005-
Disciplina 616
Soggetto topico Clinical trials
Clinical trials as Topic - methods
Research Design
Études cliniques
Étude clinique
Soggetto genere / forma Periodical
Periodicals.
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
Soggetto non controllato Medical Research
ISSN 1559-2030
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti Contemp clin trials 4
Record Nr. UNISA-996204290403316
[New York], : Elsevier, ©2005-
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Contemporary clinical trials communications [[e-journal]]
Contemporary clinical trials communications [[e-journal]]
Pubbl/distr/stampa [Amsterdam] : , : Elsevier B.V., , [2015]-
Descrizione fisica 1 online resource
Soggetto topico Clinical trials
Soggetto genere / forma Periodicals.
ISSN 2451-8654
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-996217620603316
[Amsterdam] : , : Elsevier B.V., , [2015]-
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Contemporary clinical trials communications [[e-journal]]
Contemporary clinical trials communications [[e-journal]]
Pubbl/distr/stampa [Amsterdam] : , : Elsevier B.V., , [2015]-
Descrizione fisica 1 online resource
Soggetto topico Clinical trials
Soggetto genere / forma Periodicals.
ISSN 2451-8654
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910213837003321
[Amsterdam] : , : Elsevier B.V., , [2015]-
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Controlled clinical trials
Controlled clinical trials
Pubbl/distr/stampa New York, NY, : Elsevier Science Pub. Co., ©1980-©2004
Soggetto topico Clinical trials
Controlled Clinical Trials as Topic
Études cliniques - Périodiques
Études cliniques
Soggetto genere / forma Periodical
periodicals.
Periodicals.
Périodiques.
ISSN 1879-050X
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910146790503321
New York, NY, : Elsevier Science Pub. Co., ©1980-©2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Controlled clinical trials
Controlled clinical trials
Pubbl/distr/stampa New York, NY, : Elsevier Science Pub. Co., ©1980-©2004
Soggetto topico Clinical trials
Controlled Clinical Trials as Topic
Études cliniques - Périodiques
Études cliniques
Soggetto genere / forma Periodical
periodicals.
Periodicals.
Périodiques.
ISSN 1879-050X
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-996218518903316
New York, NY, : Elsevier Science Pub. Co., ©1980-©2004
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Cross-over trials in clinical research [[electronic resource] /] / Stephen Senn
Cross-over trials in clinical research [[electronic resource] /] / Stephen Senn
Autore Senn Stephen
Edizione [2nd ed.]
Pubbl/distr/stampa Chichester ; ; Hoboken, NJ, : J. Wiley, c2002
Descrizione fisica 1 online resource (363 p.)
Disciplina 615.19
615.5/07/2
Collana Statistics in practice
Soggetto topico Crossover trials
Clinical trials
Soggetto genere / forma Electronic books.
ISBN 1-280-27006-3
9786610270064
0-470-35829-7
0-470-85458-8
0-470-85459-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cross-over Trials in Clinical Research; Contents; Preface to the second edition; Preface to the first edition; 1 Introduction; 1.1 The purpose of this chapter; 1.2 An example; 1.3 Why are cross-over trials performed?; 1.4 What are the disadvantages of cross-over trials?; 1.5 Where are cross-over trials useful?; 1.6 What attitude to cross-over trials will be adopted in this book?; 1.7 Carry-over; 1.8 What may be done about carry-over?; 1.9 Other attitudes to be adopted; 1.10 Where else can one find out about cross-over trials?
2 Some basic considerations concerning estimation in clinical trials*2.1 The purpose of this chapter; 2.2 Assumed background knowledge; 2.3 Control in clinical trials; 2.4 Two purposes of estimation; 2.5 Some features of estimation; 2.6 Practical consequences for cross-over trials; 3 The AB/BA design with Normal data; 3.1 An example; 3.2 A simple analysis ignoring the effect of period; 3.3 Student's approach*; 3.4 Assumptions in the matched-pairs t approach; 3.5 Adjusting for a period effect: two-sample t approach; 3.6 Adjusting for a period effect: the Hills-Armitage approach
3.7 Examining period effects3.8 Testing for carry-over and/or treatment by period interaction*; 3.9 A model for the AB/BA cross-over*; 3.10 Carry-over or treatment by period interaction?*; 3.11 Confidence intervals for carry-over*; 3.12 Are unbiased estimators of the treatment effect available?*; 3.13 Can we adjust for carry-over?*; 3.14 The two-stage analysis*; 3.15 Correcting the two-stage procedure*; 3.16 Use of baseline measurements; 3.17 A Bayesian approach; 3.18 Computer analysis; 3.19 Further reading; 3.20 Recommendations; Appendix 3.1 Analysis with GenStat®
Appendix 3.2 Analysis with S-Plus®4 Other outcomes and the AB/BA design; 4.1 Introduction; 4.2 Transformations; 4.3 Non-parametric methods; 4.4 Binary outcomes; 4.5 Ordered categorical data; 4.6 Frequency data; 4.7 'Survival' data*; 4.8 Final remarks; Appendix 4.1 Analysis with GenStat®; Appendix 4.2 Analysis with S-Plus®; 5 Normal data from designs with three or more treatments; 5.1 Why do we have designs with three or more treatments?; 5.2 Sequences for trials with three or more treatments; 5.3 Analyses ignoring the effect of period; 5.4 Allowing for period effects
5.5 Other miscellaneous issues5.6 Recommendations; Appendix 5.1 Analysis with GenStat®; Appendix 5.2 Analysis with S-Plus®; 6 Other outcomes from designs with three or more treatments; 6.1 Introduction; 6.2 Analyses which take no account of period effects; 6.3 Non-parametric analyses adjusting for period effects; 6.4 Hodges-Lehmann type estimators*; 6.5 A stratified period adjusted sign test; 6.6 Binary data; 6.7 Other analyses; Appendix 6.1 Analysis with GenStat®; Appendix 6.2 Analysis with S-Plus®; 7 Some special designs; 7.1 The scope of this chapter; 7.2 Factorial designs
7.3 Incomplete block designs
Record Nr. UNINA-9910143510703321
Senn Stephen  
Chichester ; ; Hoboken, NJ, : J. Wiley, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cross-over trials in clinical research [[electronic resource] /] / Stephen Senn
Cross-over trials in clinical research [[electronic resource] /] / Stephen Senn
Autore Senn Stephen
Edizione [2nd ed.]
Pubbl/distr/stampa Chichester ; ; Hoboken, NJ, : J. Wiley, c2002
Descrizione fisica 1 online resource (363 p.)
Disciplina 615.19
615.5/07/2
Collana Statistics in practice
Soggetto topico Crossover trials
Clinical trials
ISBN 1-280-27006-3
9786610270064
0-470-35829-7
0-470-85458-8
0-470-85459-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cross-over Trials in Clinical Research; Contents; Preface to the second edition; Preface to the first edition; 1 Introduction; 1.1 The purpose of this chapter; 1.2 An example; 1.3 Why are cross-over trials performed?; 1.4 What are the disadvantages of cross-over trials?; 1.5 Where are cross-over trials useful?; 1.6 What attitude to cross-over trials will be adopted in this book?; 1.7 Carry-over; 1.8 What may be done about carry-over?; 1.9 Other attitudes to be adopted; 1.10 Where else can one find out about cross-over trials?
2 Some basic considerations concerning estimation in clinical trials*2.1 The purpose of this chapter; 2.2 Assumed background knowledge; 2.3 Control in clinical trials; 2.4 Two purposes of estimation; 2.5 Some features of estimation; 2.6 Practical consequences for cross-over trials; 3 The AB/BA design with Normal data; 3.1 An example; 3.2 A simple analysis ignoring the effect of period; 3.3 Student's approach*; 3.4 Assumptions in the matched-pairs t approach; 3.5 Adjusting for a period effect: two-sample t approach; 3.6 Adjusting for a period effect: the Hills-Armitage approach
3.7 Examining period effects3.8 Testing for carry-over and/or treatment by period interaction*; 3.9 A model for the AB/BA cross-over*; 3.10 Carry-over or treatment by period interaction?*; 3.11 Confidence intervals for carry-over*; 3.12 Are unbiased estimators of the treatment effect available?*; 3.13 Can we adjust for carry-over?*; 3.14 The two-stage analysis*; 3.15 Correcting the two-stage procedure*; 3.16 Use of baseline measurements; 3.17 A Bayesian approach; 3.18 Computer analysis; 3.19 Further reading; 3.20 Recommendations; Appendix 3.1 Analysis with GenStat®
Appendix 3.2 Analysis with S-Plus®4 Other outcomes and the AB/BA design; 4.1 Introduction; 4.2 Transformations; 4.3 Non-parametric methods; 4.4 Binary outcomes; 4.5 Ordered categorical data; 4.6 Frequency data; 4.7 'Survival' data*; 4.8 Final remarks; Appendix 4.1 Analysis with GenStat®; Appendix 4.2 Analysis with S-Plus®; 5 Normal data from designs with three or more treatments; 5.1 Why do we have designs with three or more treatments?; 5.2 Sequences for trials with three or more treatments; 5.3 Analyses ignoring the effect of period; 5.4 Allowing for period effects
5.5 Other miscellaneous issues5.6 Recommendations; Appendix 5.1 Analysis with GenStat®; Appendix 5.2 Analysis with S-Plus®; 6 Other outcomes from designs with three or more treatments; 6.1 Introduction; 6.2 Analyses which take no account of period effects; 6.3 Non-parametric analyses adjusting for period effects; 6.4 Hodges-Lehmann type estimators*; 6.5 A stratified period adjusted sign test; 6.6 Binary data; 6.7 Other analyses; Appendix 6.1 Analysis with GenStat®; Appendix 6.2 Analysis with S-Plus®; 7 Some special designs; 7.1 The scope of this chapter; 7.2 Factorial designs
7.3 Incomplete block designs
Record Nr. UNINA-9910830408003321
Senn Stephen  
Chichester ; ; Hoboken, NJ, : J. Wiley, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cross-over trials in clinical research [[electronic resource] /] / Stephen Senn
Cross-over trials in clinical research [[electronic resource] /] / Stephen Senn
Autore Senn Stephen
Edizione [2nd ed.]
Pubbl/distr/stampa Chichester ; ; Hoboken, NJ, : J. Wiley, c2002
Descrizione fisica 1 online resource (363 p.)
Disciplina 615.19
615.5/07/2
Collana Statistics in practice
Soggetto topico Crossover trials
Clinical trials
ISBN 1-280-27006-3
9786610270064
0-470-35829-7
0-470-85458-8
0-470-85459-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cross-over Trials in Clinical Research; Contents; Preface to the second edition; Preface to the first edition; 1 Introduction; 1.1 The purpose of this chapter; 1.2 An example; 1.3 Why are cross-over trials performed?; 1.4 What are the disadvantages of cross-over trials?; 1.5 Where are cross-over trials useful?; 1.6 What attitude to cross-over trials will be adopted in this book?; 1.7 Carry-over; 1.8 What may be done about carry-over?; 1.9 Other attitudes to be adopted; 1.10 Where else can one find out about cross-over trials?
2 Some basic considerations concerning estimation in clinical trials*2.1 The purpose of this chapter; 2.2 Assumed background knowledge; 2.3 Control in clinical trials; 2.4 Two purposes of estimation; 2.5 Some features of estimation; 2.6 Practical consequences for cross-over trials; 3 The AB/BA design with Normal data; 3.1 An example; 3.2 A simple analysis ignoring the effect of period; 3.3 Student's approach*; 3.4 Assumptions in the matched-pairs t approach; 3.5 Adjusting for a period effect: two-sample t approach; 3.6 Adjusting for a period effect: the Hills-Armitage approach
3.7 Examining period effects3.8 Testing for carry-over and/or treatment by period interaction*; 3.9 A model for the AB/BA cross-over*; 3.10 Carry-over or treatment by period interaction?*; 3.11 Confidence intervals for carry-over*; 3.12 Are unbiased estimators of the treatment effect available?*; 3.13 Can we adjust for carry-over?*; 3.14 The two-stage analysis*; 3.15 Correcting the two-stage procedure*; 3.16 Use of baseline measurements; 3.17 A Bayesian approach; 3.18 Computer analysis; 3.19 Further reading; 3.20 Recommendations; Appendix 3.1 Analysis with GenStat®
Appendix 3.2 Analysis with S-Plus®4 Other outcomes and the AB/BA design; 4.1 Introduction; 4.2 Transformations; 4.3 Non-parametric methods; 4.4 Binary outcomes; 4.5 Ordered categorical data; 4.6 Frequency data; 4.7 'Survival' data*; 4.8 Final remarks; Appendix 4.1 Analysis with GenStat®; Appendix 4.2 Analysis with S-Plus®; 5 Normal data from designs with three or more treatments; 5.1 Why do we have designs with three or more treatments?; 5.2 Sequences for trials with three or more treatments; 5.3 Analyses ignoring the effect of period; 5.4 Allowing for period effects
5.5 Other miscellaneous issues5.6 Recommendations; Appendix 5.1 Analysis with GenStat®; Appendix 5.2 Analysis with S-Plus®; 6 Other outcomes from designs with three or more treatments; 6.1 Introduction; 6.2 Analyses which take no account of period effects; 6.3 Non-parametric analyses adjusting for period effects; 6.4 Hodges-Lehmann type estimators*; 6.5 A stratified period adjusted sign test; 6.6 Binary data; 6.7 Other analyses; Appendix 6.1 Analysis with GenStat®; Appendix 6.2 Analysis with S-Plus®; 7 Some special designs; 7.1 The scope of this chapter; 7.2 Factorial designs
7.3 Incomplete block designs
Record Nr. UNINA-9910840829603321
Senn Stephen  
Chichester ; ; Hoboken, NJ, : J. Wiley, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui