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Status unknownNCT06398951HFNCUpdated May 3, 2024

HFNC vs Two Nare HFNC in Extubated Patients

An interventional study of Two nare high flow nasal cannula in Oxygen Deficiency, sponsored by Peninsula Health. Status unknown at 1 site in Australia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-05-03.

Sponsored by Peninsula Health · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2024), so the status shown — last known as Active, not recruiting — may be out of date.

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Jul 2023, registered Mar 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

High flow nasal cannula (HFNC) are introduced to clinical practice to improve oxygenation. Our group were the first to report the use of HFNC in extubated patients that showed comparable delivery of oxygen and improved comfort. These HFNC are subsequently shown to be useful in several clinical conditions in critically ill patients including respiratory failure due to hypoxia, hypercapnia (exacerbation of chronic obstructive lung disease), or post-extubation, pre-intubation oxygenation, and others.

Recently a new mode of high flow oxygen therapy has been presented on the market where the prongs of high flow have two different diameters. These two-nare size high flow nasal cannula are capable of delivering gases at a flow rate of 15-50 L/min, similar to the conventional HFNP but the difference in the diameters provide different levels of positive pressure as compared to conventional HFNP. This positive pressure could help in gas exchange of patients who need more oxygen. These devices are approved by the Therapeutic Goods Administration (TGA); the medicine and therapeutic regulatory agency of the Australian Government.

Our aim is to compare the two size nare high flow nasal cannula with conventional high flow nasal cannula in extubated patients in intensive care unit in a randomised crossover trial. The comparison will include arterial blood gasses, physiological data including heart rate, respiratory rate, saturations as well as comfort and tolerance of the patients to two size nare high flow nasal cannuale.

Read the detailed description

This is a randomised crossover study of ventilated patients suitable for extubation was conducted. Potential patients were clinically assessed for suitability of extubation and arterial blood gasses (ABG) were performed prior to extubation to ensure the patients had optimal gas exchange. If found to be suitable for extubation, patients were extubated and were provided with a high flow blend of oxygen and air by a high flow face mask at a rate of 40 litres per minute delivering an FiO2 to ensure an oxygen saturation of 93% + 1 for 30 minutes. At the end of this 30 minute stabilization, ABG were performed and heart rate, blood pressure, and Glasgow coma score (GCS) were recorded. If the patients remained stable they were randomized to either protocol A (Duet HFNP for 30 minutes followed by conventional HFNP for 30 minutes) or protocol B ( conventional HFNP for 30 minutes followed by Duet HFNP for 30 minutes). During both protocols gas flow rate and FiO2 were maintained at exactly the same settings as used during the stabilization period. Blood gases and other physiological observations (heart rate, blood pressure, and respiratory rate, saturations, GCS, comfort score and tolerance score) were recorded at the end of each protocol. The bed side nurse assessed comfort and tolerance of patients to both the devices by a 5-point Likert scale as shown below. For the purpose of this study only medium size cannulas were used to maintain consistency. Subgroup Comparisions will be performed between those with and without nasogastric tubes and between male and female patients. Randomization is performed using sequentially numbered, sealed, opaque envelope to maintain allocation concealment.

Determine patient's comfort:

Patients provided the comfort for both duet HFNP and conventional HFNP prongs using a 5-point Likert scale;

  1. No discomfort,
  2. Little bit discomfort,
  3. Little more discomfort,
  4. Whole lot more discomfort
  5. Worst discomfort.

Determine patient's tolerance:

The bedside nurse documented the patient's tolerance using a 5-point Likert scale.

0 Patient never removes the apparatus and does not complain

  1. Patient complains about keeping apparatus on
  2. Patient request removal of the apparatus
  3. Removal of the apparatus by the patient once
  4. Removal of multiple times or non-compliance.
02

Conditions studied

  • Oxygen Deficiency

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03

In context

Hypoxia

1,245 studies on the registry are indexed under Hypoxia; 239 are open to participants now.

This study's enrollment of 50 is above the median of 45 across 864 interventional studies indexed under Hypoxia.

Browse Hypoxia studies →

Lead sponsor

Peninsula Health is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All intubated patients imminently requiring extubation with family consent for admittance into the trial that meet the follow criteria:
  • P/F ratio between > 150 prior to extubation
  • Has a functional arterial catheter to allow sample of arterial blood gasses.

Exclusion criteria

Exclusion Criteria:

  • Patients being extubated due to withdrawal of therapy Patients being extubated, that are expected to imminently die post extubation P/F Ratio :\< 150 Patients extubated on to non-invasive ventilation Patients with known epistaxis or nasal surgery.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Active comparator
    Two Nare (Duet) high flow nasal cannula

    Recently a new mode of high flow oxygen therapy has presented on the market where the cannula of high flow have different diameters. Left cannula larger in diameter than the right. These two-nare size high flow nasal cannula are capable of delivering gases at a flow rate of 15-60 L/min, similar to the conventional HFNP but the difference in the diameters provide different levels of positive pressure as compared to conventional HFNP. The two nare nasal cannula will be used for 30 minutes to assess the gas exchange, hemodynamic parameters, the tolerance and comfort of the device to the patient.

    Device: Two nare high flow nasal cannula

  • Placebo comparator
    Conventional High flow nasal cannula

    Conventional high flow nasal cannula that has been used for many years will be compared with two-nare high flow nasal cannula. The two nare nasal cannula will be used for 30 minutes to assess the gas exchange, hemodynamic parameters, the tolerance and comfort of the device to the patient.

    Device: Two nare high flow nasal cannula

Interventions

  • DeviceTwo nare high flow nasal cannula

    Recently a new mode of high flow oxygen therapy has presented on the market where the prongs of high flow have different diameters .These two-nare size high flow nasal cannula are capable of delivering gases at a flow rate of 15-50 L/min, similar to the conventional HFNP but the difference in the diameters provide different levels of positive pressure as compared to conventional HFNP.

06

What researchers measure

Primary outcomes

  1. Blood gasses (PaO2 in mmHg)

    To compare if there is difference in PaO2 between two nare and connventional high flow nasal cannula.

    Time frame: 30 minutes each for a total of one hour.

  2. Blood gasses (PaCO2 in mmHg)

    To compare if there is difference in PaCO2 between two nare and connventional high flow nasal cannula.

    Time frame: 30 minutes each for a total of one hour.

  3. Blood gasses (SaO2 percentage)

    To compare if there is difference in SaO2 between two nare and connventional high flow nasal cannula.

    Time frame: 30 minutes each for a total of one hour.

Secondary outcomes

  1. blood pressure (mmHg)

    To compare if there is difference in blood pressure between two nare and connventional high flow nasal cannula.

    Time frame: 30 minutes each for a total of one hour.

  2. Respiratory rate (breaths per minute)

    To compare if there is difference in respiratory rate between two nare and connventional high flow nasal cannula.

    Time frame: 30 minutes each for a total of one hour.

  3. Tolerance as assessed by a 5-point Likert scale ranging from 0-4.

    To compare if there is difference in tolerance assessed by bedside nurse between two nare and connventional high flow nasal cannula.

    Time frame: 30 minutes each for a total of one hour.

  4. Comfort as assessed by a 5-point Likert scale ranging from 1-5.

    To compare if there is difference in comfort as reported by the patient between two nare and connventional high flow nasal cannula.

    Time frame: 30 minutes each for a total of one hour.

07

Study locations

1 site
  • Frankston Hospital
    Frankston, Victoria 3199, Australia
08

References and documents

Publications

  • Tiruvoipati R, Reddy MP, Paul E, Gupta S, Subramaniam A, Zhang D, Haji K. A comparison of conventional high-flow nasal cannula vs the duet high-flow nasal cannula in extubated patients: a randomized crossover trial. Eur J Med Res. 2025 Mar 26;30(1):205. doi: 10.1186/s40001-025-02447-0. PubMed 40140950 ↗

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06398951
Lead sponsor
Peninsula Health
Responsible party
Sponsor
First posted
May 3, 2024
Start date
Jul 1, 2023
Primary completion
Sep 1, 2025 (estimated)
Completion
Sep 1, 2025 (estimated)
Last update
May 3, 2024

Study contacts

RAVINDRANATH TIRUVOIPATI, PhD
principal investigator · Peninsula Health

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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