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Clinical trials : a methodologic perspective / Steven Piantadosi.

By: Piantadosi, Steven.
Series: Wiley series in probability and statistics. Publisher: Hoboken, N.J. : Wiley-Interscience, c2005Edition: 2nd ed.Description: xxvii, 687 p. : ill. ; 26 cm.ISBN: 0471727814 (hbk.); 9780471727811 (hbk.).Subject(s): Clinical trials -- Statistical methodsDDC classification: 610.72
Contents:
Preface. - Preface to the first edition. - 1. Preliminaries. - 2. Clinical trials as research. - 3. Why clinical trials are ethical? - 4. Contexts for clinical trials. - 5. Statistical perspectives. - 6. Clinical trials as experimental designs. - 7. Random error and bias. - 8. Objectives and outcomes. - 9. Translational clinical trials. - 10. Dose-finding designs. - 11. Sample size and power. - 12. The study cohort. - 13. Treatment allocation. - 14. Treatment effects monitoring. - 15. Counting subjects and events. - 16. Estimating clinical effects. - 17. Prognostic factor analyses. - 18. Reporting and authorship. - 19. Factorial designs. - 20. Crossover designs. - 21. Meta-analyses. - 22. Misconduct and fraud in clinical research. - Appendices. A: Data and program. - B: Notation and terminology. - C: Abbreviations. - D: Nuremberg code. - E: Declaration of Helsinki. - F: NCI Data and Safety Monitoring Policy. G: NIH data and Safety Monitoring Policy - H: Royal statistical society code of conduct. - Bibliography. - Author index. - Subject index.
Item type Current location Call number Copy number Status Notes Date due Barcode Remark
Main Collection TU External Storage-LCS
610.72 PIA (Browse shelf) 1 Available SBSxx,36100,03,GR 5000081538 Please fill up online form at https://taylorslibrary.taylors.edu.my/services/external_storage1

Includes bibliographical references (p. 613-658 ) and indexes.

Preface. - Preface to the first edition. - 1. Preliminaries. - 2. Clinical trials as research. - 3. Why clinical trials are ethical? - 4. Contexts for clinical trials. - 5. Statistical perspectives. - 6. Clinical trials as experimental designs. - 7. Random error and bias. - 8. Objectives and outcomes. - 9. Translational clinical trials. - 10. Dose-finding designs. - 11. Sample size and power. - 12. The study cohort. - 13. Treatment allocation. - 14. Treatment effects monitoring. - 15. Counting subjects and events. - 16. Estimating clinical effects. - 17. Prognostic factor analyses. - 18. Reporting and authorship. - 19. Factorial designs. - 20. Crossover designs. - 21. Meta-analyses. - 22. Misconduct and fraud in clinical research. - Appendices. A: Data and program. - B: Notation and terminology. - C: Abbreviations. - D: Nuremberg code. - E: Declaration of Helsinki. - F: NCI Data and Safety Monitoring Policy. G: NIH data and Safety Monitoring Policy - H: Royal statistical society code of conduct. - Bibliography. - Author index. - Subject index.