Table 3.
Secondary outcomes
| Outcome | Spironolactone (%) | Placebo (%) | Unadjusted odds ratio (95% CI) | Adjusted* odds ratio (95% CI) |
|---|---|---|---|---|
| Self-assessed overall improvement score of 3-6: | ||||
| 12 weeks | 122/169 (72) | 108/159 (68) | 1.23 (0.76 to 1.96) | 1.16 (0.70 to 1.91) |
| 24 weeks | 131/160 (82) | 81/128 (63) | 2.62 (1.53 to 4.50) | 2.72 (1.50 to 4.93)† |
| Satisfaction with trial treatment, score 3-5: | ||||
| 24 weeks | 101/143 (71) | 53/123 (43) | 3.18 (1.91 to 5.27) | 3.12 (1.80 to 5.41)† |
| PGA success score: | ||||
| 12 weeks | 36/176 (21) | 20/166 (12) | 1.91 (1.05 to 3.45) | 1.69 (0.89 to 3.19) |
| 24 weeks | 53/164 (32) | 15/136 (11) | 3.93 (2.09 to 7.37) | 3.76 (1.95 to 7.28)† |
| IGA success score: | ||||
| 12 weeks | 31/168 (19) | 9/160 (6) | 3.78 (1.73 to 8.27) | 5.18 (2.18 to 12.28)† |
Data are number of participants/total number (percentage), unless otherwise specified. CI=confidence interval; IGA=investigator’s global assessment; PGA=participant’s global assessment; QoL=quality of life.
Adjusted for stratification factors (site and baseline severity (IGA <3 versus 3 or more)), baseline Acne-QoL symptom subscale score, topical treatment use (yes/no to using any topical treatment), hormonal treatment, age, and polycystic ovary syndrome status.
Statistically significant differences indicated.