drugset / Trial / NCT02182505
Safety and Efficacy of Berodual® Inhaled Via Respimat® Compared to MDI (Metered Dose Inhaler) in Pediatric Patients With Asthma
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |