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Table 2 Comparisons between groups at the end of the study

From: Step-down from high dose fixed combination therapy in asthma patients: a randomized controlled trial

 

BDP/F

400/24 μg/day (N = 206)

FP/S

500/100 μg/day (N = 216)

Between group

p value

FEV1, L

2.92 (0.04)

2.92 (0.03)

0.938

FEV1% predicted

85.90 (0.98)

85.70 (0.98)

0.878

PEF, L/min

442.47 (4.57)

440.21 (4.55)

0.699

PEF % predicted

96.87 (1.46)

98.43 (1.32)

0.428

Daytime symptoms scorea

1.37 (0.07)

1.32 (0.06)

0.609

Night-time symptom scorea

1.33 (0.11)

1.46 (0.10)

0.368

symptom-free days, %

93.66 (1.13)

92.47 (1.11)

0.451

Controlled asthmab, n (%)

163 (90.0)

167 (85.2)

0.362

Partly controlled asthmab, %

11 (6.0)

18 (9.2)

 

Uncontrolled asthmab, %

7 (4.0)

11 (5.6)

 
  1. The values are adjusted means (SE). The lung function values were measured during the last visit. a the mean of the last 4 weeks of treatment derived from diary cards, b in the last 4 weeks of the treatment period. BDP/F, beclomethasone dipropionate/formoterol; FP/S, fluticasone propionate/salmeterol; FEV1, forced expiratory volume in 1 second; PEF, peak expiratory flow.