Design of studies for medical research

Bibliographic Information

Design of studies for medical research

David Machlin, Michael J. Campbell

Wiley, c2005

Available at  / 7 libraries

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Note

Includes bibliographical references (p. [246]-254) and index

Description and Table of Contents

Description

The same careful rigour imposed on the design of phase III randomised controlled trials is not always applied to medical research in other areas such as trials conducted at earlier stages of drug development. With the emphasis that is now placed on evidence-based medicine, such care and rigour will inevitably impact on these areas with increasing attention turned to the quality of design. This title describes what principles can be used to structure research effectively allowing for the required degree of accuracy. Written by two best selling authors, this book includes many examples from medical literature and will be of great value to all groups conducting studies at the interface of clinical and laboratory research.

Table of Contents

Preface. Chapter 1. What is Evidence. Chapter 2. Measurement, Forms and Questionnaires. Chapter 3. Principles of Study Size Calculation. Chapter 4. Randomisation. Chapter 5. Cross-sectional Longitudinal Studies. Chapter 6. Surveys, Cohort and Case-Control Studies. Chapter 7. Clinical Trails - General Issues. Chapter 8. Early Clinical Trials. Chapter 9. Phase III Trials. Chapter 10. Diagnosis. Chapter 11. Prognostic Factor Studies. References. Tables. Index.

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Details

  • NCID
    BA72002107
  • ISBN
    • 0470844957
  • LCCN
    2004065408
  • Country Code
    uk
  • Title Language Code
    eng
  • Text Language Code
    eng
  • Place of Publication
    Chichester, West Sussex
  • Pages/Volumes
    274 p.
  • Size
    25 cm
  • Classification
  • Subject Headings
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