drugset / Trial / NCT03839433

The Mannitol-Asthma-Ciclesonide-Study

NCT03839433

Phase 4 Completed 72 enrolled Cantonal Hosptal, Baselland
RandomizedParallel-groupDouble-blindTreatment

Summary

Response of a 4 weeks treatment with daily once 320 µg ciclesonide on airway hyperresponsiveness assessed with mannitol. Hypothesis: Treatment with inhaled ciclesonide reduces airway hyper-responsiveness in 80% of hyper-responsive patients compared to 20% only in the placebo group and the group without airway hyper-responsiveness.

Timeline

Start
2007-06
Primary completion
2008-08
Completion
2008-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ciclesonide Other / unclassified 320 ug Inhaled

Indications