Spiriva® 18µg Once Daily in Chinese COPD Patients of Different Disease Severities
NCT00621582 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4918
Last updated 2014-10-23
Summary
The objective of the present Post Marketing Surveillance Study (PMS) study is to evaluate safety and effectiveness of tiotropium bromide (Spiriva®) 18 µg once daily in 5,000 patients with COPD of varying severities over 8 weeks.
Conditions
- Pulmonary Disease, Chronic Obstructive
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Boehringer Ingelheim · Boehringer Ingelheim
Eligibility
- Min Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-05-31
- Primary Completion
- 2008-02-29
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