About this trial
This is a registry-based, randomized, controlled clinical trial of the effect of added high-flow oxygen therapy (using the device Lumis HFT) during one year in people with long-term oxygen therapy (LTOT) for chronic obstructive pulmonary disease (COPD) or interstitial lung disease (ILD).
Eligibility criteria
Qualifiers
Age 40 years or older
Ongoing LTOT: prescribed for at least 15 hours per day; and since at least 28 days as registered in Swedevox
COPD or ILD as main underlying reason for LTOT
Oxygen concentrator as stationary oxygen source in the home including night-time
Disqualifiers
Current or previous treatment with home HFOT
Current treatment with home mechanical ventilation
Current treatment with home CPAP
Hospitalized during the last 2 weeks
Trial design
Treatments tested in this trial
- Added high-flow oxygen therapy
- Standard care
Treatment groups
Sponsors and collaborators
Skane University Hospital
Lead sponsor
Uppsala University Hospital
Collaborator
Region Stockholm
Collaborator
Region Örebro County
Collaborator
Blekinge County Council Hospital
Collaborator
Blekinge Institute of Technology
Collaborator
Lund University
Collaborator
Region Östergötland
Collaborator
Vastra Gotaland Region
Collaborator
Region Västerbotten
Collaborator
Landstinget i Värmland
Collaborator
ResMed
Collaborator
Swedish Heart Lung Foundation
Collaborator
The Swedish Research Council
Collaborator