Journal of Clinical Epidemiology
Volume 61, Issue 3 , Pages 241-246, March 2008

Early stopping of randomized clinical trials for overt efficacy is problematic

  • Dirk Bassler

      Affiliations

    • Department of Neonatology, University Children's Hospital, Tübingen, Germany
  • ,
  • Victor M. Montori

      Affiliations

    • Knowledge and Encounter Research Unit, Division of Endocrinology and Internal Medicine, Mayo Clinic College of Medicine, Rochester, MN, USA
  • ,
  • Matthias Briel

      Affiliations

    • CLARITY Research Group, Department of Clinical Epidemiology and Biostatistics, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada
    • Basel Institute for Clinical Epidemiology, University Hospital, Basel, Switzerland
  • ,
  • Paul Glasziou

      Affiliations

    • Centre for Evidence-Based Medicine, Department of Primary Health Care, University of Oxford, Oxford, UK
  • ,
  • Gordon Guyatt

      Affiliations

    • CLARITY Research Group, Department of Clinical Epidemiology and Biostatistics, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada
    • Corresponding Author InformationCorresponding author. Department of Clinical Epidemiology and Biostatistics, Health Sciences Centre, Room 2C12, McMaster University, Hamilton, Ontario, Canada. Tel.: +905-525-9140 ext. 22900; fax: +905-524-3841.

Accepted 22 July 2007.

Abstract 

Objective

To illustrate controversial issues associated with stopping randomized controlled trials (RCTs) early for apparent benefit.

Study Design and Setting

The article presents our review of prior relevant work and our research group's reflections on early stopping.

Results

Compelling evidence suggests that trials stopped early for benefit systematically overestimate treatment effects, sometimes by a large amount. Unresolved controversies in trials stopped early for benefit include ethical and statistical problems in the interpretation of results.

Conclusions

The best strategy to minimize the problems associated with early stopping of RCTs for benefit is not to stop early. As an alternative, we suggest a threefold approach: a low P-value as the threshold for stopping at the time of interim analyses, not to look before a sufficiently large number of events has accrued and continuation of enrollment and follow-up for a further period.

Keywords: Randomized controlled trial, Data-monitoring committee, Stopping rule, Interim analysis, Stopping for benefit, STOPIT-2

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 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.
 

PII: S0895-4356(07)00292-2

doi:10.1016/j.jclinepi.2007.07.016

Journal of Clinical Epidemiology
Volume 61, Issue 3 , Pages 241-246, March 2008