Spiriva® in Patients With Chronic Obstructive Pulmonary Disease (COPD)
Tolerability and Efficacy of Spiriva® 18 Micrograms in Patients With COPD in Daily Practice
1 other identifier
observational
63,127
0 countries
N/A
Brief Summary
As part of the post-marketing surveillance, information is to be gathered regarding the tolerance and efficacy of Spiriva® 18 micrograms in patients with COPD under conditions of daily practice
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2002
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2003
CompletedFirst Submitted
Initial submission to the registry
June 20, 2014
CompletedFirst Posted
Study publicly available on registry
June 24, 2014
CompletedJune 24, 2014
June 1, 2014
1.3 years
June 20, 2014
June 20, 2014
Conditions
Outcome Measures
Primary Outcomes (6)
Change from baseline in breathlessness when walking/climbing stairs
Baseline, after 4 weeks
Change from baseline in overall severity of the clinical picture
Baseline, after 4 weeks of treatment
Occurrence of Adverse Events
up to 4 weeks
Change from baseline in breathlessness on Physical exercise
Baseline, after 4 weeks
Change from baseline in breathlessness during housework
Baseline, after 4 weeks
Change from baseline in breathlessness during everyday activities
Baseline, after 4 weeks
Study Arms (1)
Symptoms of COPD
Patients with symptoms of COPD receiving Tiotropium bromide 18 micrograms
Interventions
Tiotropium bromide18 micrograms (capsule with powder for inhalation)
Eligibility Criteria
You may qualify if:
- Men and women aged at least 40 years presenting with the symptoms of COPD
You may not qualify if:
- Patients presenting with the general and specific contraindications listed in the Patient Information Leaflet and the Basic Product Information
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 20, 2014
First Posted
June 24, 2014
Study Start
June 1, 2002
Primary Completion
October 1, 2003
Last Updated
June 24, 2014
Record last verified: 2014-06