Table 2.
Primary efficacy endpoint: clinical success outcome at the end of the study.
| Population | Clindamycin [% (95% CI)] | Amoxicillin/clavulanic acid [% (95% CI)] | Treatment difference | ||
|---|---|---|---|---|---|
| Miettinen and Nurminen method (primary) [% (95% CI)] | Farrington and Manning method [% (95% CI)] | Two-sample proportion test [% (95% CI)] | |||
| PP | 89.7% (84.6%, 93.5%) |
88.2% (83.0%, 92.2%) | 1.5% ( 95 CI: −4.7%, 7.7%) | 1.5% (−4.9%, 8.0%) |
1.5% (−4.5%, 7.6%) |
|
| |||||
| ITT-E | 86.4% (81.3%, 90.5%) |
85.5% (80.3%, 89.8%) | 0.9% (−5.5%, 7.3%) | 0.9% (−5.6%, 7.4%) |
0.9% (−5.5%, 7.2%) |
|
| |||||
| ITT (randomised treatment arm) | 85.7% (80.5%, 89.9%) |
83.3% (77.9%, 87.9%) | 2.3% (−4.3%, 9.0%) | 2.3% (−4.4%, 9.0%) |
2.3% (−4.2%, 8.9%) |