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The Effect of HFNC on Exercise Capacity Compared to VM in COPD Patients Recovering From Acute Evacerbation

G

Guangzhou Medical University

Status

Unknown

Conditions

COPD

Treatments

Device: high flow nasal cannula
Device: Venturi mask

Study type

Interventional

Funder types

Other

Identifiers

NCT05097560
FAHGZ-20210811

Details and patient eligibility

About

Early PR is thought to be effective in COPD patients recovering from acute exacerbation, while the effect of HFNC during exercise training in these patients remains unclear. The study may provide evidence of early PR in COPD patients recovering from acute exacerbation.

Full description

We hypothesize that HFNC may increases exercise time in COPD patients recovering from acute exacerbation compare to VM. A randomized, cross-over clinical trial in which either HFNC or VM may be used as an adjunct in 10-MST in random order, respectively, will be performed to compare the endurance time. The physiological effect of HFNC and VM during exercise will also be measured to explore the mechanism.

Enrollment

10 estimated patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • hospitalized AECOPD patients
  • be ambulatory by 48h after admission for AECOPD
  • requires oxygen by screening exercise test

Exclusion criteria

  • active coronary ischemia
  • respiratory diseases other than COPD
  • unstable vital signs
  • unstable psychological status

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

10 participants in 2 patient groups

HFNC group
Experimental group
Description:
* Set FiO2 28% * Titrate the flow of HFNC at the highest tolerated value up to 60 L/min
Treatment:
Device: high flow nasal cannula
VM group
Active Comparator group
Description:
- Keep FiO2 constant with VM and HFNC during the two trial
Treatment:
Device: Venturi mask

Trial contacts and locations

1

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Central trial contact

Shiying Fang, MD

Data sourced from clinicaltrials.gov

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