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A Comparison of Symbicort Single Inhaler Therapy (Symbicort Turbohaler 160/4.5 μg, 1 Inhalation b.i.d. Plus as Needed) and Conventional Best Practice for the Treatment of Persistent Asthma in Adolescents and Adults - a 26-week, Randomised, Open-label, Parallel-group, Multi-centre Study (SALTO)

NCT00290264 Phase 3 COMPLETED

The primary objective is to compare the efficacy of Symbicort Single inhaler Therapy with treatment according to conventional best practice in adolescent and adult patients with persistent asthma.

Details

Lead sponsorAstraZeneca
PhasePhase 3
StatusCOMPLETED
Enrolment1000
Start date2004-12
Completion2006-08

Conditions

Interventions

Primary outcomes

Countries

Belgium, Luxembourg