Study identifier:RO-2455-402-DE
ClinicalTrials.gov identifier:NCT01285180
EudraCT identifier:N/A
CTIS identifier:N/A
Daxas in COPD Therapy
Severe COPD
-
No
Daxas
All
5472
Observational
18 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Sept 2016 by AstraZeneca
AstraZeneca
-
Daxas (roflumilast) is the first oral anti-inflammatory phosphodiesterase inhibitor (PDE-4) for patients with severe chronic obstructive pulmonary disease (COPD) experiencing chronic cough and sputum and with a history of exacerbations as add-on to bronchodilator treatment. With its mode of action Daxas can reduce exacerbations rates and improve lung function parameters which may result in a better health-related quality of life and an improved long-term management of COPD. 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. Evaluation is based on two COPD specific questionnaires to assess the patient`s health status over six months. During the study, socio-demographic data and cost-of-illness data will be recorded. Daxas (tablet) will be administered once daily. The study will provide further data on the safety and tolerability of Daxas.
Location
Location
Dresden, Germany, 01069
Location
Dresden, Germany, 01097
Location
Dresden, Germany, 01099
Location
Dresden, Germany, 01109
Location
Dresden, Germany, 01129
Location
Dresden, Germany, 01139
Location
Dresden, Germany, 01156
Location
Dresden, Germany, 01157
Arms | Assigned Interventions |
---|---|
DINO | Drug: Daxas 500 microgram, oral, once daily as add-on therapy to existing therapy |
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