Table 2.
Study parameters | Bron et al. [39] | Assil et al. [7] | Kavuncu et al. [40] | Yaylali et al. [41] | Hirneiss et al. [42] |
---|---|---|---|---|---|
Comparator | Placebo | Placebo | PA | PA | PA and ketorolac |
No. of patients | 182 | 197 | 80 | 48 | 45 |
Treatment duration (weeks) | 2 | Up to 2 | 2 | 2 | 4 |
Patients with resolution of ACIa at final visit ( %) | Rimexolone—60 % | Rimexolone—60 % | Not reportedb | Not reportedb | Not reportedb |
Vehicle—28 % | Placebo—32 % | ||||
Mean IOP at final visit | No perceptible changes in IOP | Mean decrease in IOP in both treatment groups compared to baseline | Rimexolone—13.0 ± 3.2 mmHg | Rimexolone—11.6 ± 1.4 mmHg | Rimexolone—13.25 mmHg |
PA group—14.60 mmHg | |||||
PA group—11.7 ± 2.9 mmHg | PA group—10.8 ± 1.3 mmHg | Ketorolac group—13.73 mmHg | |||
Clinically significant increases in IOP (≥ 10 mmHg) | Not reported | n = 2 for rimexolone; | Not reported | Not reported | Not reported |
n = 2 for placebo |
ACI anterior chamber inflammation, IOP intraocular pressure, PA prednisolone acetate
aResolution of ACI defined as anterior chamber cell count <5 and flare Grade 0 (none)
bThe study did not report the percentages of patients with resolution of ACI; instead, mean cell and flare at study visits were reported