Pulmonary Disease, Chronic Obstructive Clinical Trial
Official title:
Assessment of Physical Functioning and Handling of Spiolto® Respimat® in Patients With Chronic Obstructive Pulmonary Disease (COPD) Requiring Long-acting Dual Bronchodilation in Routine Clinical Practice
The primary objective of this Non Interventional Study is to measure changes in physical
functioning, a surrogate for physical activity and exercise capacity, in COPD patients on
treatment with Spiolto® Respimat® in routine daily treatment after approximately 6 weeks.
A secondary objective is to evaluate the patient's general condition (physician's evaluation)
from Visit 1 (baseline visit at the start of the study) to Visit 2 (final visit at the end of
the study, approx. 6 weeks after Visit 1), as well as patient satisfaction with Spiolto®
Respimat® at Visit 2.
n/a
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