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Table 1 Baseline characteristics of the UPLIFT® study population

From: Defining a COPD composite safety endpoint for demonstrating efficacy in clinical trials: results from the randomized, placebo-controlled UPLIFT® trial

 

Tiotropium (n = 2986)

Control (n = 3006)

Total (N = 5992)

Male, %

75

74

75

Mean (SD) age, y

65 (8)

65 (8)

65 (8)

Current smoker, %

29

30

30

Mean (SD) duration of COPD, y

10 (8)

10 (7)

10 (7)

GOLD stage, %

   

 II

46

45

46

 III

44

44

44

 IV

8

9

9

Mean (SD) prebronchodilator

 

 FEV1, L

1.1 (0.4)

1.1 (0.4)

1.1 (0.4)

 FEV1, % predicted value

40 (12)

39 (12)

39 (12)

 FVC, L

2.6 (0.8)

2.6 (0.8)

2.6 (0.8)

 FEV1/FVC ratio, %

42 (11)

42 (11)

42 (11)

Mean (SD) postbronchodilator

 

 FEV1, L

1.3 (0.4)

1.3 (0.4)

1.3 (0.4)

 FEV1, % predicted value

48 (13)

47 (13)

48 (13)

 FVC, L

3.1 (0.9)

3.1 (0.9)

3.1 (0.9)

 FEV1/FVC ratio, %

44 (11)

43 (11)

43 (11)

Mean (SD) SGRQ total score, units

46 (17)

46 (17)

46 (17)

Patients with comorbidities, n (%)

   

 Vascular disorders

1353 (45.3)

1367 (45.5)

2720 (45.4)

 Cardiac disorders

790 (26.5)

765 (25.5)

1555 (26.0)

 Respiratory, thoracic and mediastinal disorders

565 (18.9)

593 (19.7)

1158 (19.3)

  1. COPD chronic obstructive pulmonary disease, FEV 1 forced expiratory volume in 1 s, FVC forced vital capacity, GOLD Global Initiative for Chronic Obstructive Lung Disease, SD standard deviation, SGRQ St George’s Respiratory Questionnaire