A Concise Guide to Clinical Trials - Allan Hackshaw

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Résumé :

Preface ix

Foreword xi

1 Fundamental concepts 1

1.1 What is a clinical trial? 1

1.2 Early trials 2

1.3 Why clinical trials are needed 3

1.4 Alternatives to clinical trials 3

1.5 Types of clinical trials 5

1.6 Key design features 7

1.7 Summary points 13

2 Types of outcome measures and understanding them 15

2.1 Clinical trial outcome measures (endpoints) 15

2.2 'True' versus surrogate outcome measures 16

2.3 Types of outcomes 18

2.4 Counting people 18

2.5 Taking measurements on people 19

2.6 Time-to-event measures 21

2.7 Patient-reported outcome measures (PROMs) 25

2.8 Summary points 27

3 Phase I trials 29

3.1 Trial objectives 29

3.2 Types of participants 30

3.3 Outcome measures 30

3.4 Designs 32

3.5 Conducting the trial 37

3.6 Statistical analysis and reporting the trial results 37

3.7 Summary points 39

4 Phase II trials 41

4.1 Trial objectives 41

4.2 Designs 41

4.3 Outcome measures 48

4.4 Estimating study size 48

4.5 Stopping early for toxicity 50

4.6 Statistical analyses 51

4.7 Interpreting phase II studies 55

4.8 Summary points 56

5 Phase III trials: design 59

5.1 Trial objectives 59

5.2 Designs 59

5.3 Inclusion and exclusion criteria 62

5.4 Experimental/investigational treatment group 64

5.5 Control (comparator) group 64

5.6 Randomisation and allocating participants 65

5.7 Blinding (placebo) 66

5.8 Outcome measures 66

5.9 Participant follow-up 68

5.10 Estimating study size 69

5.11 Non-inferiority and equivalence 72

5.12 Multiplicity: multiple treatment arms or multiple outcome measures 74

5.13 Participants who switch trial interventions (crossover) 75

5.14 Summary points 76

6 Phase III trials - fundamental aspects of analysis and interpretation 79

6.1 Efficacy 79

6.2 Safety toxicity and adverse events 96

6.3 Adherence (compliance) 98

6.4 Health?related quality of life (QoL) 99

6.5 Intention?t?treat and per?protocol analyses 102

6.6 Summary points 103

7 Randomised trials - additional aspects of analysis and interpretation 107

7.1 Non-inferiority and equivalence trials 107

7.2 Composite outcome measures 110

7.3 Subgroup (subset) analyses 111

7.4 Crossover trials 115

7.5 Factorial trials 115

7.6 Cluster randomised trial 117

7.7 Repeated measures 117

7.8 Multiple endpoints 117

7.9 Dealing with missing outcome data 119

7.10 Translational research 120

8 Commercial trials of medicinal products...

Biographie:
health economic analysis 127

8.1 Commercial trials of medicines (drugs) 127

8.2 Other types of interventions 135

Surgical techniques 137

Radiotherapy and radioactive substances 139

Behavioural/lifestyle interventions 139

Medical devices 141

Cell and gene therapy 142

8.3 Health economic analyses 144

9 Systematic reviews and meta-analyses...