| Group A | Group B | DIfference Group B – Group A |
---|
| T0 | T1 | Difference T1 – T0 |
p
| T0 | T1 | Difference T1 – T0 |
p-value | Difference T1-T0 |
p-value |
---|
FEV1 (L) mean (±SE) | 2.52 (±0.13) | 2.62 (±0.12) | 0.10 | 0.519 | 2.51 (±0.12) | 2.72 (±0.13) | 0.21 | 0.229 | 0.11 | 0.007 |
FEV1 (%), mean (±SE) | 82.40 (±1.63) | 87.08 (±1.58) | 4.68 | 0.043 | 81.93 (±2.00) | 89.50 (±2.64) | 7.57 | 0.009 | 2.89 | 0.04 |
- T0 =at baseline, before Beclomethasone dipropionate/Formoterol and Fluticasone furoate/Vilanterol treatment
- T1 = after 12 weeks of Beclomethasone dipropionate/Formoterol and Fluticasone furoate/Vilanterol treatment
- Forced expiratory volume in 1 s, litres, FEV1 (L)
- Forced expiratory volume in 1 s, predicted values, FEV1(%)
- [95 % CI, confidence interval]
-
p refers to Wilcoxon rank-sum test
- Group A: patients treated with Beclomethasone dipropionate/Formoterol 100/6 μg b.i.d
- Group B: patients treated with Fluticasone furoate/Vilanterol 92/22 μg once-a-day