Status:
COMPLETED
Berodual® Respimat® Solution for Inhalation in Patients With Chronic Obstructive Airways Disease
Lead Sponsor:
Boehringer Ingelheim
Conditions:
Pulmonary Disease, Chronic Obstructive
Eligibility:
All Genders
Brief Summary
Tolerability, efficacy and handling of Berodual® Respimat® 20/50µg/dose solution for inhalation in patients with chronic obstructive airways disease in daily practice
Eligibility Criteria
Inclusion
- Men and women presenting with symptoms of chronic obstructive pulmonary disease
- Both previously untreated patients and patients treated previously with Berodual® or with other anti-obstructive respiratory tract agents may be included
Exclusion
- Patients presenting with the general and specific contraindications listed in the Patient Information Leaflet and the Basic Product Information
Key Trial Info
Start Date :
March 1 2004
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
4602 Patients enrolled
Trial Details
Trial ID
NCT02231372
Start Date
March 1 2004
Last Update
September 4 2014
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