Specific Use-result Surveillance of Spiriva Respimat in Asthmatics
NCT02489981 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 359
Last updated 2019-02-11
Summary
The safety of Spiriva® 2.5 µg Respimat® 60 puffs (hereinafter referred to as Spiriva® Respimat®) in patients with severe persistent asthma under the real-world use was not confirmed in clinical trials.
Conditions
Interventions
- DRUG
-
Spiriva
60 puffs
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Boehringer Ingelheim · Boehringer Ingelheim
Eligibility
- Min Age
- 15 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-06-01
- Primary Completion
- 2017-08-01
- Completion
- 2017-09-28
Countries
- Brazil
Study Locations
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