Clinical Trials Directory

Trials / Terminated

TerminatedNCT04840706

Open-Label Prospective Study Comparing Long-Term Outcome With or Without HFNC in Patients With Stable Hypercapnic COPD

Open-Label Prospective Study Comparing Long-Term Outcome With or Without High-flow Nasal Cannula AirvoTM in Patients With Stable Hypercapnic COPD

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
3 (actual)
Sponsor
Turku University Hospital · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aims of the study are to compare long-term one-year outcome with or without AirvoTM in stabile hypercapnic COPD patients, who are non-compliant to NIV after an acute exacerbation of COPD.

Detailed description

When compared to NIV, much less experience is available from clinical studies on HFNC therapy. Until now, few studies have investigated the effect of HFNC therapy on hypercapnic COPD patients and the number of patients recruited in these studies is limited. AirvoTM therapy could be good choice of treatment for those COPD patients that are not compliant to NIV but need treatment for hypercapnia in order to reduce COPD exacerbations and enhance QOL.The aims of the study are to compare long-term one-year outcome with or without AirvoTM in stabile hypercapnic COPD patients, who are non-compliant to NIV after an acute exacerbation of COPD.

Conditions

Interventions

TypeNameDescription
DEVICEHFNC AirvoHFNC device (Airvo) long-term use in in stabile hypercapnic COPD patients, who are non-compliant to NIV after an acute exacerbation of COPD
OTHERStandard careNo HFNC treatment

Timeline

Start date
2022-04-21
Primary completion
2024-04-30
Completion
2024-04-30
First posted
2021-04-12
Last updated
2025-12-29

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT04840706. Inclusion in this directory is not an endorsement.