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The Edi Level and Cardiopulmonary Function Between HHHFNC and Unheated Humidified High-Flow Oxygen Mask in COPD

F

Fu Jen Catholic University

Status

Terminated

Conditions

Respiratory Insufficiency
Chronic Obstructive Lung Disease

Treatments

Device: UHFOM
Device: HHHFNC

Study type

Interventional

Funder types

Other

Identifiers

NCT03811158
PL-201705001-M

Details and patient eligibility

About

Patients with COPD exacerbation usually need respiratory support after extubation. Recently, HHHFNC has been used in both adult and neonates with post-extubation respiratory support. Studies indicate that HHHFNC has seminar efficacy compared to non-invasive positive pressure ventilation and superior than conventional oxygen therapy. There are no clinical data of diaphragm electrical activity and cardiopulmonary function for using HHHFNC and UHFOM as post-extubation respiratory support.

Full description

Objectives: The aim of this study is to compare the Edi level and cardiopulmonary parameters between heated humidified high-flow nasal cannula (HHHFNC) versus unheated high-flow oxygen mask (UHFOM) in acute exacerbation of chronic obstructive pulmonary disease (COPD) patients with post-extubation respiratory support. This is the first clinical trial to investigate and analysis the variations of cardiopulmonary parameters and Edi level between HHHFNC and UHFOM in adult patients.

Enrollment

2 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. AE of COPD received intubation and ready to be weaning
  2. P/F ratio > 200 during SBT before extubation

Exclusion criteria

  1. Unable to insert NG tube
  2. Refuse to re-intubated when respiratory failure after extubation
  3. Planned NIV use after extubation
  4. Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

2 participants in 2 patient groups

HHHFNC group
Experimental group
Description:
On HHHFNC FiO2 will setting as same as SBT before extubation Flow rate: 50L/min
Treatment:
Device: HHHFNC
UHFOM group
Sham Comparator group
Description:
On Aerosol mask FiO2 will setting as same as SBT before extubation Flow rate: 15L/min
Treatment:
Device: UHFOM

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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