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Clinical Trial Summary

The primary objective of this non-interventional study (NIS) is to evaluate changes within 3 months in quality of life according to health status evaluated with the COPD Assessment Test (CAT) in COPD patients who have recently switched (within one week) from tiotropium monotherapy (Spiriva® Handihaler®) to dual therapy with tiotropium bromide plus olodaterol (Spiolto® Respimat®), in the Greek private and public sector pulmonary offices and clinics.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04672941
Study type Observational
Source Boehringer Ingelheim
Contact
Status Completed
Phase
Start date February 16, 2021
Completion date February 21, 2022

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