The purpose of this study is to evaluate the level of satisfaction experienced by asthma or chronic obstructive pulmonary disease (COPD) patients when using the Fluticasone/Salmeterol HFA Metered Dose Inhaler (MDI) with counter, as compared to using Fluticasone/Salmeterol HFA MDI without counter.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
132
Fluticasone/Salmeterol HFA, 2 puffs twice daily
GSK Investigational Site
Auchenflower, Queensland, Australia
GSK Investigational Site
Caboolture, Queensland, Australia
GSK Investigational Site
Kippa-Ring, Queensland, Australia
GSK Investigational Site
Perth, Western Australia, Australia
Patient satisfaction questionnaires administered at baseline and at the end of treatment (day 30).
Time frame: Day 30
Healthcare professional satisfaction questionnaires administered at baseline and at the end of treatment (day 30) Patient compliance as measured by the device counter readings at the end of treatment (day 30), compared to the baseline reading.
Time frame: Day 30
Healthcare professional satisfaction questionnaires Patient Compliance Safety Evaluations: adverse events
Time frame: 8 months
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