Table 1

Ocular adverse event rates from hypothetical randomised controlled trial scenarios comparing a 12-week course of two IOP-lowering drugs for open-angle glaucoma

ScenarioDrug A
n/N (%)
Drug B
n/N (%)
Difference in percentages
(95% CI)
p Value
11/30 (3)8/30 (27)−23 (−41 to −5)0.026
24/30 (13)10/30 (33)−20 (−40 to 2)0.125
328/300 (9)45/300 (15)−6 (−11 to −0.4)0.045
46/300 (2)9/300 (3)−1 (−4 to 2)0.603
  • Calculations were carried out in Stata6 using command csi and rdcii; the p value is from a two-sided Fisher's exact test and the CI for the percentage difference is from Newcombe's Method 107.

  • IOP, intraocular pressure; n, number of adverse events; N, number of patients.