Fundamentals of randomized clinical trials in wound care design and conduct

Anne M Eskes, Fleur E Brölmann, Bauer E Sumpio, Dieter Mayer, Zena Moore, Magnus S Agren, Michel Hermans, Keith Cutting, Dink A Legemate, Dirk T Ubbink, Hester Vermeulen

Research output: Contribution to journalArticleAcademicpeer-review

18 Citations (Scopus)

Abstract

The care for chronic and acute wounds is a substantial problem around the world. This has led to a plethora of products to accelerate healing. Unfortunately, the quality of studies evaluating the efficacy of such wound care products is frequently low. Randomized clinical trials are universally acknowledged as the study design of choice for comparing treatment effects, as they eliminate several sources of bias. We propose a framework for the design and conduct of future randomized clinical trials that will offer strong scientific evidence for the effectiveness of wound care interventions. While randomization is a necessary feature of a robust comparative study, it is not sufficient to ensure a study at low risk of bias. Randomized clinical trials should also ensure adequate allocation concealment and blinding of outcome assessors, apply intention-to-treat analysis, and use patient-oriented outcomes. This article proposes strategies for improving the evidence base for wound care decision making.

Original languageEnglish
Pages (from-to)449-55
Number of pages7
JournalWound repair and regeneration
Volume20
Issue number4
DOIs
Publication statusPublished - 31 May 2012

Keywords

  • Anti-Bacterial Agents
  • Anti-Infective Agents, Local
  • Checklist
  • Debridement
  • Delivery of Health Care
  • Evidence-Based Medicine
  • Female
  • Humans
  • Journal Article
  • Male
  • Postoperative Complications
  • Randomized Controlled Trials as Topic
  • Wound Healing
  • Wounds and Injuries

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