The American Journal of Medicine
Volume 111, Issue 7 , Pages 553-558, November 2001

Active-control equivalence trials and antihypertensive agents

  • Finlay A McAlister, MD, MSc

      Affiliations

    • Corresponding Author InformationRequests for reprints should be addressed to Finlay A. McAlister, MD, MSc, 2E3.24 WMC, University of Alberta Hospital, 8440 112 Street, Edmonton, Alberta, Canada T6G 2R7.
    • Division of General Internal Medicine, University of Alberta (FAM), Alberta, Canada
    • The Institute of Health Economics (FAM), Edmonton, Alberta, Canada
  • ,
  • David L Sackett, MD, MSc

      Affiliations

    • Trout Research and Education Centre at Irish Lake (DLS), Ontario, Canada

Received 21 March 2001; received in revised form 7 July 2001; accepted 10 July 2001.

Abstract 

Purpose

To identify methodological features that affect the validity of conclusions drawn from active-control equivalence trials and to apply these criteria to recently published trials comparing antihypertensive agents from different classes.

Methods

Standard methodological criteria for randomized clinical trials and six additional methodological features that affect the validity of active-control equivalence trials were applied to four recently published large trials that compared different antihypertensive classes and that concluded that their results showed equivalence.

Results

All four of these trials fulfilled standard criteria for randomized trials. However, none fulfilled all of the six additional methodological criteria that affect the validity of active-control equivalence trials, one fulfilled five criteria, two fulfilled two criteria, and one failed to fulfill any of the criteria.

Conclusion

Standard methodological criteria for evaluating superiority trials are inadequate for the interpretation of active-control equivalence trials. The methodological criteria outlined in this article for judging the validity of active-control equivalence trials are not specific to antihypertensive trials and may be applied to trials that test a wide variety of interventions.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 30.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 
  • 1 Finlay A. McAlister, MD, MSc, is a population health investigator for the Alberta Heritage Foundation for Medical Research.

PII: S0002-9343(01)00900-7

The American Journal of Medicine
Volume 111, Issue 7 , Pages 553-558, November 2001