Thromb Haemost 1987; 58(04): 953-956
DOI: 10.1055/s-0038-1646033
Review Article
Schattauer GmbH Stuttgart

Sample Size in the Planning and Interpretation of Clinical Trials

Authors

  • Mark N levine

    The Departments of Medicine and Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, Ontario, Canada
  • Jack Hirsh

    The Departments of Medicine and Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, Ontario, Canada
Further Information

Publication History

Received 14 May 1987

Accepted after revision 09 October 1987

Publication Date:
29 June 2018 (online)

Preview

Abstract

An understanding of sample size determination is important in both planning and interpreting the results of clinical trials. A Type II error occurs when it is concluded that there is no difference between treatment groups, when in truth there is a difference. Such a false negative conclusion results from too few patients in a trial. In this review the principles of estimating sample size before a trial is commenced and evaluating the results of a negative completed trial are reviewed. Clinically relevant examples are used to illustrate these concepts.