Clinical Trial

Asymmetric High-Flow Nasal Cannula During Pulmonary Rehabilitation in COPD

Study acronym: A-HFNC-PR
Completed
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Summary
This randomized pilot trial evaluated the feasibility and preliminary effects of using asymmetric high-flow nasal cannula (A-HFNC) during exercise-based pulmonary rehabilitation (PR) in patients with chronic obstructive pulmonary disease (COPD). Thirty patients were randomly assigned to conventional PR or PR supplemented with A-HFNC during aerobic training, completing 12 supervised sessions. The study assessed whether A-HFNC could be safely and acceptably incorporated into PR, and whether it enabled higher training intensity and improved exercise performance. Results showed that the intervention was feasible and safe, with 83% adherence in both groups and no adverse events. Patients in the A-HFNC group trained at significantly higher treadmill inclination and showed a clinically meaningful trend toward greater improvement in maximal exercise tolerance. These findings support the design of a larger definitive trial.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-03-22.
Trial Details
NCT Number NCT07497230
Lead Sponsor Universidad de Santiago de Chile
Conditions Pulmonary Disease, Chronic Obstructive (COPD), Dyspnea, Exercise Tolerance, Rehabilitation
Enrollment 30 participants
Start Date 2025-05-02
Primary Completion 2025-09-20 (estimated)
Study Completion 2025-09-20 (estimated)
Updated on ClinicalTrials.gov 2026-04-01