The primary objective of this study is to examine efficacy and safety of tiotropium compared to plac ebo as add-on therapy in severe asthmatics according to GINA step 4 classification
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
115
Boehringer Ingelheim Investigational Site
Aalborg, Denmark
Boehringer Ingelheim Investigational Site
Aarhus C, Denmark
Boehringer Ingelheim Investigational Site
The primary efficacy endpoint is the FEV1 response (within 3 hours post dosing) determined at the end of the 8-week treatment period
FEV1 and FVC AUC 0-3h (in a subset 0-24h) PEF, use of rescue medication, daytime and nocturnal symptoms etc.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Hvidovre, Denmark
Boehringer Ingelheim Investigational Site
K?benhavn NV, Denmark
Boehringer Ingelheim Investigational Site
Odense C, Denmark
Boehringer Ingelheim Investigational Site
Gelnhausen, Germany
Boehringer Ingelheim Investigational Site
Gro?hansdorf, Germany
Boehringer Ingelheim Investigational Site
Rüdersdorf, Germany
Boehringer Ingelheim Investigational Site
Wiesbaden, Germany
Boehringer Ingelheim Investigational Site
Wiesloch, Germany
...and 6 more locations