Study identifier:RO-2455-401-DE
ClinicalTrials.gov identifier:NCT01285167
EudraCT identifier:N/A
CTIS identifier:N/A
Daxas for COPD therapy (DACOTA)
Chronic Obstructive Pulmonary Disease
-
No
Daxas
All
3645
Observational
18 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Sept 2016 by AstraZeneca
AstraZeneca
-
Chronic obstructive pulmonary disease (COPD) is a progressive and largely irreversible lung disease characterized by chronic bronchitis and/or emphysema, resulting in breathlessness, cough and sputum. As COPD progresses, patients experience increasing deterioration of their health-related quality of life, with greater impairment in their ability to work and declining participation in social and physical activities. The aim of this non-interventional study is to evaluate data on quality of life in COPD patients in Germany in a real life medical setting under therapy with the phosphodiesterase-inhibitor (PDE-4) roflumilast (Daxas). Evaluation is based on two COPD specific questionnaires to assess the patient`s health status over six months. During the study, lung function measurements such as spirometry will be conducted according to common medical standard. Daxas (tablet) will be administered once daily. The study will provide further data on the safety and tolerability of Daxas.
Location
Location
Dresden, Germany, 01099
Location
Dresden, Germany, 01187
Location
Dresden, Germany, 01307
Location
Radebeul, Germany, 01445
Location
Riesa, Germany, 01591
Location
Nossen, Germany, 01683
Location
Sebnitz, Germany, 01855
Location
Kamenz, Germany, 01917
Arms | Assigned Interventions |
---|---|
DACOTA | Drug: Daxas 500 microgram, oral, once daily as add-on therapy to existing therapy |
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