drugset / Trial / NCT02182505

Safety and Efficacy of Berodual® Inhaled Via Respimat® Compared to MDI (Metered Dose Inhaler) in Pediatric Patients With Asthma

NCT02182505

Phase 3 Completed 535 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Study to demonstrate that at least one of the two doses of Berodual® (50 µg fenoterol hydrobromide + 20 µg ipratropium bromide and 25 µg fenoterol hydrobromide + 10 µg ipratropium bromide, 1 puff t.i.d.) administered via Respimat® device gives a bronchodilator response which is not inferior to that obtained from one dose of Berodual® (50 µg fenoterol hydrobromide + 21 µg ipratropium bromide, 2 puffs t.i.d.) administered via the MDI (chlorofluorocarbon-metered dose inhaler) with Aerochamber® and that the safety profile is at least as good when paediatric asthma patients are treated for four weeks.

Timeline

Start
1998-09
Primary completion
1999-07
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Fenoterol Unknown 25 ug Inhaled
Subject Fenoterol Unknown 50 ug Inhaled
Subject Ipratropium Small molecule 10 ug Inhaled
Subject Ipratropium Small molecule 20 ug Inhaled
Subject Ipratropium Small molecule 21 ug Inhaled

Indications