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. 2017 Mar 11;44(7):774–782. doi: 10.1111/1346-8138.13798

Table 3.

Absolute number and percentage reduction of total lesions and non‐inflammatory lesions (FAS)

Cohorts Baseline, no. of lesions End of study, no. of lesions Absolute reduction, no. lesions Percentage reduction, %
No. of TL
2.5% BPO gel (203 cases) 50 (40–63) 21 (10–35) 29*** (17 to 38) 62.2*** (33.3 to 79.6)
Difference from placebo −16 16 (12 to 20) 29.4 (22.7 to 36.5)
5% BPO gel (203 cases) 51 (40–64) 18 (8–30) 31*** (23 to 43) 67.9*** (48.6 to 81.8)
Difference from placebo −18 20 (16 to 24) 36.0 (29.3 to 42.9)
Placebo 51 (41–67) 36 (22–59) 14 (−2 to 28) 28.6 (−3.9 to 54.4)
No. of non‐IL
2.5% BPO gel (203 cases) 29 (23–40) 14 (7–25) 16*** (7 to 24) 56.5*** (26.3 to 78.3)
Difference from placebo −10 10 (7 to 13) 29.5 (21.4 to 37.6)
5% BPO gel (203 cases) 30 (23–41) 11 (6–21) 19*** (12 to 26) 68.2*** (38.7 to 81.4)
Difference from placebo −12 13 (10 to 16) 37.5 (29.7 to 45.2)
Placebo 30 (23–43) 25 (14–41) 7 (−4 to 17) 21.9 (−13.0 to 53.3)

***Median (interquartile range). Difference from placebo: Hodges–Lehmann estimator (95% confidence intervals). P < 0.001 vs placebo (Wilcoxon two sample test). Difference from placebo: Hodges‐Lehmann estimator (95% confidence intervals). P < 0.001 vs placebo (Wilcoxon two sample test). BPO, benzoyl peroxide; FAS, full analysis set; IL, inflammatory lesions; SD, standard deviation; TL, total lesions.