Other active comparator
Cyproterone ethinylestradiol
OTHER_ACTIVE_cyproterone_ethinylestradiol
Related
Effects across outcomes
Bayesian random effects estimate against the comparator of each analysis (usually placebo), posterior median and 95% credible interval. Green: clearly better; red: clearly worse.
| Condition | Outcome | Window | Versus | Effect (95% CrI) | SUCRA |
|---|---|---|---|---|---|
| Polycystic ovary syndrome | Nausea | longest follow-up | Placebo | HR 0.20 (0.00 to 3.83) | 0.94 |
| Polycystic ovary syndrome | Vomiting | longest follow-up | Placebo | HR 0.21 (0.00 to 4.39) | 0.95 |
| Polycystic ovary syndrome | Diarrhea | longest follow-up | Placebo | HR 0.14 (0.00 to 2.35) | 0.96 |
| Polycystic ovary syndrome | Regular menstrual cycles | weeks 12 to 52 (target week 26) | Standard care or no added treatment | OR 1.76 (0.19 to 15.44) | 0.53 |