Overview
Spiriva® in Patients With Chronic Obstructive Pulmonary Disease (COPD)
Status:
Completed
Completed
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
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 practiceAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Boehringer IngelheimTreatments:
Bromides
Tiotropium Bromide
Criteria
Inclusion Criteria:- Men and women aged at least 40 years presenting with the symptoms of COPD
Exclusion Criteria:
- Patients presenting with the general and specific contraindications listed in the
Patient Information Leaflet and the Basic Product Information