The aim of the study is to compare the efficacy of roflumilast on pulmonary function and symptomatic parameters in patients with chronic obstructive pulmonary disease (COPD) during concomitant administration of salmeterol. The study duration will last up to 28 weeks. The study will provide further data on safety and tolerability of roflumilast.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
933
500 µg, once daily, oral administration in the morning
once daily
Pre-bronchodilator Forced Expiratory Volume in First Second (FEV1)
Mean change from baseline during the treatment period in pre-bronchodilator FEV1 \[L\]
Time frame: Change from baseline over 24 weeks of treatment
Post-bronchodilator FEV1
Mean change from baseline during the treatment period in post-bronchodilator FEV1 \[L\]
Time frame: Change from baseline over 24 weeks of treatment
COPD Exacerbation Rate (Mild, Moderate or Severe)
Mean rate of COPD exacerbations requiring rescue medication of 3 or more puffs/day on at least 2 consecutive days (=mild COPD exacerbations), or requiring oral or parenteral glucocorticosteroids (=moderate COPD exacerbations), or requiring hospitalization, or leading to death (=severe COPD exacerbations), per patient per year. A COPD exacerbation is an event in the natural course of the disease characterized by a change in the patient's baseline dyspnea, cough and/or sputum beyond day-to-day variability sufficient to warrant a change in management \[ATS / ERS 2005\].
Time frame: 24 weeks treatment period
Transition Dyspnea Index (TDI) Focal Score
The TDI is a recognized questionnaire to measure dyspnea in an out patient COPD population. At baseline, 3 components of dyspnea, each graded with 4 questions, were asked: - Functional Impairment - Magnitude of Task - Magnitude of Effort At each of the post-randomization visits questions from the TDI were asked related to 3 components: Change in - Functional Impairment - Magnitude of Task - Magnitude of Effort Each question in the TDI is graded from -3 (major deterioration) to +3 (major improvement). This results in a TDI Focal Score ranging from -9 to +9.
Time frame: Change from baseline over 24 weeks of treatment
Shortness of Breath Questionnaire (SOBQ) Total Score
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Altana Pharma/Nycomed Investigational Site
Linz, Austria
Altana Pharma/Nycomed Investigational Site
Neusiedl/See, Austria
Altana Pharma/Nycomed Investigational Site
Perg, Austria
Altana Pharma/Nycomed Investigational Site
Salzburg, Austria
Altana Pharma/Nycomed Investigational Site
Sankt Pölten, Austria
Altana Pharma/Nycomed Investigational Site
Steyr, Austria
Altana Pharma/Nycomed Investigational Site
Vienna, Austria
Altana Pharma/Nycomed Investigational Site
Vienna, Austria
Altana Pharma/Nycomed Investigational Site
Vienna, Austria
Altana Pharma/Nycomed Investigational Site
Wiener Neustadt, Austria
...and 124 more locations
Mean change from baseline during the treatment period in SOBQ. This is a 24-item measure that assesses self-reported shortness of breath while performing a variety of activities of daily living. The questions were administered at visits V0, V2, V3, V4, V5, V6 and Vend to assess the perceived shortness of breath of the patient. For each activity listed in the questionnaire the patient should rate his/her breathlessness on a scale between zero and five, where zero is "not at all breathless" and five is "maximally breathless or too breathless to do the activity".
Time frame: Change from baseline over 24 weeks of treatment