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Study identifier: NCT07192016 Synced from ClinicalTrials.gov · August 05, 2026
● Recruiting

129-Xe MRI Study of Single Triple Therapy Inhaler Effects in COPD Patients With Moderate-severe Dyspnea and/or Poor Health Status With High or Low Risk of Exacerbation

Condition: Chronic Obstructive Pulmonary Disease (COPD)  ·  Sponsor: Western University, Canada

PhasePhase 4
Planned participants60
Who can joinAll sexes, 50 Years to 85 Years
Healthy volunteersNo

About this study

The goal of this study is to study how 12-weeks daily (and optional 48-weeks) single inhaler triple therapy (fluticasone furoate (FF)-an inhaled corticosteroid; umeclidinium (UMEC)-a long-acting muscarinic antagonist; vilanterol (VI)-a long-acting β2-adrenergic agonist) works to treat adults with COPD. The investigators will compare the effects of this medication on adults with COPD who are at low risk of a flare-up and adults with COPD who are at high risk of a flare-up. The main questions it aims to answer are: * Does FF/UMEC/VI improve ventilation defect percent as measured on 129-Xenon MRI in adults with moderate-severe COPD * Evaluate the relationships between the ventilation defect percent and lung function test results Participants will: * Take the inhaler FF/UMEC/VI once daily for 12-weeks (optional 48-weeks) * visit Robarts 2 times (with optional 3rd visit) for tests and imaging

This description comes directly from the study's public registry record.

Talk to the study team

Grace E Parraga, PhD  ·  519-931-5265  ·  gparraga@uwo.ca

Angela Wilson, RRT  ·  519-931-5777  ·  awilson@robarts.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Robarts Research Institute; The University of Western Ontario; London Health Sciences CentreLondon, Ontario, CanadaRecruiting

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