drugset / Trial / NCT00826969

Ciclesonide for the Treatment of Airway Hyperresponsiveness

NCT00826969

Phase 4 Completed 64 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

The study objective is to investigate in a placebo-controlled, double-blind manner the effect of inhaled corticosteroid (ciclesonide) on airway hyperresponsiveness measured as having PD15 mannitol. Treatment medication will be administered as follows: 320 microgram ciclesonide or placebo will be inhaled once daily. The study duration consists of a treatment period of 4 weeks. The study will provide further data on safety of ciclesonide.

Timeline

Start
2008-09
Primary completion
2010-07
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ciclesonide Other / unclassified 320 ug Inhaled

Indications