Randomized clinical trials : design, practice and reporting

著者

書誌事項

Randomized clinical trials : design, practice and reporting

David Machin, Peter M. Fayers

Wiley-Blackwell, 2010

大学図書館所蔵 件 / 全5件

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注記

Includes bibliographical references and index

In this title the authors provide step-by-step coverage of recent advances and developments in clinical trial methodology

内容説明・目次

内容説明

Using examples and case studies from industry, academia andresearch literature, Randomized Clinical Trials provides adetailed overview of the key issues involved in designing,conducting, analysing and reporting randomized clinicaltrials. It examines the methodology for conducting Phase IIIclinical trials, developing the protocols, the practice forcapturing, measuring, and analysing the resulting clinical data andtheir subsequent reporting. Randomized clinical trials are the principal method fordetermining the relative efficacy and safety of alternativetreatments, interventions or medical devices. They areconducted by groups comprising one or more of pharmaceutical andallied health-care organisations, academic institutions, andcharity supported research groups. In many cases such trialsprovide the key evidence necessary for the regulatory approval of anew product for future patient use. Randomized ClinicalTrials provides comprehensive coverage of such trials, rangingfrom elementary to advanced level. Written by authors with considerable experience of clinicaltrials, Randomized Clinical Trials is an authoritative guidefor clinicians, nurses, data managers and medical statisticiansinvolved in clinical trials research and for health careprofessionals directly involved in patient care in a clinical trialcontext.

目次

Preface. 1 Introduction. 1.1 Introduction. 1.2 Some completed trials. 1.3 Choice of design. 1.4 Practical constraints. 1.5 Influencing clinical practice. 1.6 History. 1.7 How trials arise. 1.8 Ethical considerations. 1.9 Regulatory requirements. 1.10 Focus. 1.11 Further reading. 2 Design Features. 2.1 Introduction. 2.2 The research question. 2.3 Patient selection. 2.4 The consent process. 2.5 Choice of interventions. 2.6 Choice of design. 2.7 Assigning the interventions. 2.8 Making the assessments. 2.9 Analysis and reporting. 2.10 Technical details. 2.11 Guidelines. 2.12 Further reading. 3 The Trial Protocol. 3.1 Introduction. 3.2 Protocol abstract. 3.3 Protocol background. 3.4 Protocol research objectives. 3.5 Protocol design. 3.6 Protocol intervention details. 3.7 Protocol eligibility. 3.8 Protocol randomization. 3.9 Protocol assessment and data collection. 3.10 Protocol statistical considerations. 3.11 Protocol ethical issues. 3.12 Protocol organizational structure. 3.13 Protocol publication policy. 3.14 Protocol trial forms. 3.15 Protocol appendices. 3.16 Regulatory requirements. 3.17 Guidelines. 3.18 Protocols. 4 Measurement and Data Capture. 4.1 Introduction. 4.2 Measures and endpoints. 4.3 Making the observations. 4.4 Baseline measures. 4.5 Types of measures. 4.6 Data recording. 4.7 Technical notes. 4.8 Guidelines. 5 Randomization. 5.1 Introduction. 5.2 Rationale. 5.3 Mechanics. 5.4 Application. 5.5 Carrying out randomization. 5.6 Documentation. 5.7 Unacceptable methods. 5.8 Software. 5.9 Guidelines. 6 Trial Initiation. 6.1 Introduction. 6.2 Trial organization. 6.3 Data collection and processing. 6.4 Data monitoring. 6.5 Ethical and regulatory requirements. 6.6 Launching the trial. 6.7 Trial registries. 6.8 Guidelines. 7 Trial Conduct. 7.1 Introduction. 7.2 Regular feedback. 7.3 Publicity. 7.4 Data monitoring committees. 7.5 Protocol modifications. 7.6 Preparing the publication(s). 7.7 The next trial? 7.8 Protocols. 8 Basics of Analysis. 8.1 Introduction. 8.2 Confidence intervals. 8.3 Statistical tests. 8.4 Examples of analysis. 8.5 Other issues. 8.6 Practice. 8.7 Technical details. 9 Trial Size. 9.1 Introduction. 9.2 Significance level and power. 9.3 The fundamental equation. 9.4 Specific situations. 9.5 Practical considerations. 9.6 Further topics. 9.7 Other methods and software. 9.8 Guideline. 10 Reporting. 10.1 Introduction. 10.2 Publication guidelines. 10.3 Responsibilities. 10.4 Background. 10.5 Methods. 10.6 Findings. 10.7 When things go wrong. 10.8 Conclusions. 10.9 Guidelines. 11 Adaptations of the Basic Design. 11.1 Introduction. 11.2 Repeated measures. 11.3 Cluster-randomized trials. 11.4 Non-inferiority trials. 11.5 Guidelines. 12 Paired Designs. 12.1 Cross-over trials. 12.2 Split-mouth designs. 12.3 Paired organs. 13 More Than Two Interventions. 13.1 Introduction. 13.2 Unstructured comparisons. 13.3 Comparisons with placebo (or standard). 13.4 Dose response designs. 13.5 Factorial trials. 14 Further Topics. 14.1 Introduction. 14.2 Adaptive approaches. 14.3 Large simple trials. 14.4 Bayesian methods. 14.5 Zelen randomized-consent designs. 14.6 Systematic overviews. 14.7 Conclusion. Statistical Tables. Glossary. References. Index.

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