Study identifier:D5890L00010
ClinicalTrials.gov identifier:N/A
EudraCT identifier:2005-005974-64
CTIS identifier:N/A
A comparison of Symbicort Single Inhaler Therapy (Symbicort Turbuhaler 160/4.5 micrograms, 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. Study SPAIN
ASTHMA, BRONCHIAL
Phase 3
No
Symbicort (budesonide/formoterol) Turbuhaler, Conventional treatment
All
654
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Nov 2010 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
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