Study identifier:D5890L00011
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A comparison of Symbicort Single inhaler Therapy (Symbicort Turbuhaler 160/4.5 µg, 1 inhalation b.i.d. plus as needed) and conventional best practice for the treatment of persistent asthma in adults - a 26-week, randomised, open-label, parallel-group, multicentre study
asthma
Phase 3
No
Symbicort, used twice daily (b.i.d) and as needed (prn), Budesonide Turbuhaler 200 µg, Fluticasone Discus 250 µg, Formoterol Turbuhaler 4.5 µg, Terbutaline Turbuhaler 0.5 mg, Salbutamol pressurized metered dose inhaler (pMDI) 100 µg, Salmeterol Discus 50 µg, Budesonide/Formoterol Turbuhaler 160/4.5 µg, Fluticasone/Salmeterol Discus 250/50 µg, Fluticasone/Salmeterol Discus 500/50 µg, Theophylline 200 mg, Theophylline 300 mg, Singulair 10 mg
All
1600
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The purpose of this study is to determine whether Symbicort dosed according to the Symbicort Maintenance and Reliever Therapy (SMART) concept is superior to standard asthma treatment according to the local German treatment guidelines.
Location
Location
Stuttgart, Baden-Württemberg, Germany
Location
München, Bayern, Germany
Location
Berlin, Berlin, Germany
Location
Cottbus, Brandenburg, Germany
Location
Hamburg, Hamburg, Germany
Location
Frankfurt, Hessen, Germany
Location
Rostock, Mecklenburg-Vorpommern, Germany
Location
Hannover, Niedersachsen, Germany
Arms | Assigned Interventions |
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