drugset / Trial / NCT00628758

A Comparison of Symbicort® Single Inhaler Therapy and Conventional Best Practice for the Treatment of Persistent Asthma

NCT00628758 ↗

Phase 3 Completed 430 enrolled AstraZeneca
RandomizedParallel-groupOpen-labelTreatment

Summary

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

Timeline

Start
2005-12
Primary completion
2008-09
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Background Symbicort Unknown 4.5 ug Inhaled
Background Symbicort Unknown 160 ug Inhaled
Background Astmerol Unknown — —
Background Bricanyl Unknown — —
Background Combivent® Unknown — —
Background Formoterol Other / unclassified — —
Background Salbulin Unknown — —
Background Salbutamol Unknown — —
Background Salbutamol Sustained Release Unknown — —
Background Salbutol Unknown — —
Background Seretide Unknown — —
Background Symbicort Unknown — —
Background Vent-o-sal Unknown — —
Background Ventofor Unknown — —
Background salmeterol xinafoate Unknown — —

Indications