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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 Standard Treatment for the Treatment of Persistent Asthma in Adolescents and Adults. A Randomized, Open, Parallel-group, Multicentre 26-weeks Study

NCT00242411 Phase 4 COMPLETED

The purpose of the study is to compare the efficacy of a flexible dose of Symbicort (budesonide/formoterol) with conventional stepwise best standard treatment in patients with persistent asthma.

Details

Lead sponsorAstraZeneca
PhasePhase 4
StatusCOMPLETED
Enrolment1900
Start date2004-09
Completion2006-10

Conditions

Interventions

Primary outcomes

Countries

Denmark, Finland, Norway