Dropout rates for intent-to-treat and per protocol analyses

Am J Ophthalmol. 2004 Apr;137(4):639-45. doi: 10.1016/j.ajo.2003.11.028.

Abstract

Purpose: To describe dropout rates for the intent-to-treat and per protocol analyses from prospective clinical trials.

Methods: Review of prospective multi-center parallel studies of 100 patients or more from 1996 onwards.

Results: We identified 33 articles (70 treatment arms) that fit the criteria for this study. No statistical differences in dropout rates were observed among drug classes for either the intent-to-treat (P =.075) or per protocol analyses (P =.40). A difference was observed in the percent dropout rate for the intent-to-treat analyses decreasing with the length of the study (P <.0001). This finding was not observed by the number of study visits (P =.44). However, a statistically greater percent dropout rate was observed for the per protocol analyses increasing with the length of the study (P =.034) and number of study visits (P =.01). No statistical differences were observed or with increasing sample size of the study for either the intent-to-treat or per protocol analyses (P >.05).

Conclusions: Known discontinuation rates for per protocol and intent-to-treat analyses may help in planning sample sizes for future clinical trials.

MeSH terms

  • Antihypertensive Agents / therapeutic use*
  • Clinical Protocols
  • Clinical Trials as Topic / statistics & numerical data*
  • Glaucoma / drug therapy*
  • Humans
  • Intraocular Pressure / drug effects
  • Models, Statistical
  • Ocular Hypertension / drug therapy
  • Patient Dropouts / statistics & numerical data*
  • Prospective Studies
  • Research Design
  • Sampling Studies

Substances

  • Antihypertensive Agents