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A Comparison of the Efficacy of Symbicort® Single Inhaler Therapy (Symbicort Turbuhaler® 160/4.5 mg 1 Inhalation b.i.d. Plus As-needed) and Conventional Best Practice for the Treatment of Persistent Asthma in Adolescents and Adults - a 26 Weeks, Randomised, Open-label, Parallel-group, Multicentre Study

NCT00252824 Phase 3 COMPLETED

The purpose of the study is to compare the efficacy of a flexible dose of Symbicort with conventional stepwise treatment according to asthma treatment guidelines in patients with persistent asthma

Details

Lead sponsorAstraZeneca
PhasePhase 3
StatusCOMPLETED
Enrolment1000
Start date2005-07
Completion2006-12

Conditions

Interventions

Primary outcomes

Countries

Chile, Croatia, Czechia, Greece, Iceland, Latvia, Lithuania, Portugal, Slovakia, Slovenia