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Table 1 Baseline characteristics of the patients examined, grouped based on randomised treatment

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)

Age (years)

 

44 (13)

44 (13)

Gender

Male

69 (33.5%)

77 (35.6%)

 

Female

137 (66.5%)

139 (64.4%)

BMI (kg/m2)

 

27.1 (5.1)

27.0 (5.2)

Device used before screening

pMDI

12.6%

12.6%

 

DPI

87.4%

87.4%

Years from asthma diagnosis

 

11 (10)

13 (11)

FEV1, L

 

2.9 (0.9)

3.0 (0.8)

FEV1% predicted

 

86.9 (15.1)

88.3 (14.1)

PEF, L/min

 

435.7 (8.3)

452.9 (8.1)

PEF % predicted

 

97.8 (21.4)

100.5 (20.3)

Number of days/week with symptomsa

 

0.5 (1.2)

0.3 (0.6)

Number of nights/week with symptomsa

 

0.3 (1.1)

0.1 (0.6)

Rescue medication use, puffs/weeka

 

1.2 (0.4)

1.2 (0.4)

Rescue-free days/weekb

 

6.6 (1.4)

6.6 (1.2)

PEF >80%, days/weekb

 

5.6 (1.9)

5.5 (1.6)

Controlled asthmab, n (%)

 

203 (98.5)

212 (98.1)

Partly controlled asthmab, %

 

2 (1.0)

3 (1.4)

Uncontrolled asthmab, %

 

1 (0.5)

1 (0.5)

  1. The values are means (SD). a the mean of the last 4 weeks of run-in period, b in each of the last 4 weeks of the run-in period. The lung function values were measured during the randomisation visit at the end of the run-in. BDP/F, beclomethasone dipropionate/formoterol; FP/S, fluticasone propionate/salmeterol; BMI, body mass index; FEV1, forced expiratory volume in 1 second; PEF, peak expiratory flow.