Block urn design - a new randomization algorithm for sequential trials with two or more treatments and balanced or unbalanced allocation

Contemp Clin Trials. 2011 Nov;32(6):953-61. doi: 10.1016/j.cct.2011.08.004. Epub 2011 Aug 22.

Abstract

Permuted block design is the most popular randomization method used in clinical trials, especially for trials with more than two treatments and unbalanced allocation, because of its consistent imbalance control and simplicity in implementation. However, the risk of selection biases caused by high proportion of deterministic assignments is a cause of concern. Efron's biased coin design and Wei's urn design provide better allocation randomness without deterministic assignments, but they do not consistently control treatment imbalances. Alternative randomization designs with improved performances have been proposed over the past few decades, including Soares and Wu's big stick design, which has high allocation randomness, but is limited to two-treatment balanced allocation scenarios only, and Berger's maximal procedure design which has a high allocation randomness and a potential for more general trial scenarios, but lacks the explicit function for the conditional allocation probability and is more complex to implement than most other designs. The block urn design proposed in this paper combines the advantages of existing randomization designs while overcoming their limitations. Statistical properties of the new algorithm are assessed and compared to currently available designs via analytical and computer simulation approaches. The results suggest that the block urn design simultaneously provides consistent imbalance control and high allocation randomness. It can be easily implemented for sequential clinical trials with two or more treatments and balanced or unbalanced allocation.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Algorithms*
  • Computer Simulation
  • Humans
  • Models, Statistical*
  • Probability
  • Randomized Controlled Trials as Topic / methods*
  • Selection Bias