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High Flow Nasal Cannula HFNC In Covid-19 Patients

Prone Positioning and High Flow Nasal Canula (HFNC) Therapy: A Game Changer in COVID-19 Outcome

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04560257
Acronym
HFNC19LGH
Enrollment
30
Registered
2020-09-23
Start date
2020-05-01
Completion date
2020-12-30
Last updated
2020-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

SARS-CoV Infection, SARS (Severe Acute Respiratory Syndrome)

Keywords

COVID-19, High flow nasal cannula HFNC, Clinical outcome

Brief summary

Many non-invasive ventilatory choices are available for COVID-19 patient who are having mild to moderate respiratory distress and their use will decrease the chance of ICU admission, intubation and mechanical ventilation in severe cases of COVID-19. However, all these respiratory supports and oxygen supply devices are aerosol generating and their selection should be precised enough to control nosocomial spread. High flow nasal cannula HFNC is a device that delivered the warmed and humid air on high flow rate through nose. It is used to treat severe respiratory distress in COVID-19 patients, a non-invasive ventilatory approach which is relative comfortable by using humidified and pre-heated air containing large concentration of oxygen. In acute respiratory failure HFNC is proven to be very effective and it also reduced the need of mechanical ventilation in severe patients. Apart from the supply of oxygen, HFNC generating positive airway pressure and decreasing the rebreathing from anatomical dead space. Prone position is also a save therapy and has been proven to be effective for refractory hypoxia by increasing tidal volume, oxygenation and diaphragmatic functions in ARDS patients. Recent studies showed that prone positioning and HFNC might avoid the prerequisite of intubation in moderate to severe patients of ARDS and as a result it decreases the nosocomial infection in physicians who are doing these aerosol generating procedures.

Detailed description

This is observational single-center study, that will be done at Lahore General Hospital in which 95 beds are allocated for COVID-19 patients including ICUs and HDUs. Ethical approval will be obtained from research ethical committee of Lahore General hospital, Lahore. Informed consent will be obtained from all patients who will agree to publish their data in this research. We will protect patient's privacy and obey with the Helsinki Declaration.

Interventions

High flow nasal cannula HFNC is a device that delivered the warmed and humid air on high flow rate through nose. It is used to treat severe respiratory distress in COVID-19 patients, a non-invasive ventilatory approach which is relative comfortable by using humidified and pre-heated air containing large concentration of oxygen.

Sponsors

Lahore General Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

quasi- experimental

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* All patients of \> 18 years of ages, males and females who will be diagnosed COVID-19 positive by RT-PCR with moderate illness. * Patients having classical radiological lesions of COVID-19 on X-ray chest or HRCT chest. * Respiratory rate \> 30/ min and not responding to non-rebreather masks. * COVID-related pneumonia requiring non-invasive ventilatory support (high-flow nasal cannula, and / or non-invasive ventilation and / or CPAP)

Exclusion criteria

* Inability to provide consent; * Severe respiratory failure requiring invasive ventilatory support; * Indication of immediate tracheal intubation * Significant acute progressive circulatory insufficiency * Impaired alertness, confusion, restlessness * Chest trauma or other contraindication to prone position * Pneumothorax * Nasal blockade * Unable to tolerate high flow oxygen

Design outcomes

Primary

MeasureTime frameDescription
Clinical response of HFNC10 daysThe number of patients treated with non-invasive ventilation devices. HFNC related events (hot air feeling, nasal lesions)

Secondary

MeasureTime frameDescription
Duration of intervention15 daysLength of HFNC therapy to COVID-19 patients
Duration of hospitalization15 daysNumber of days of hospital admission either in ICU or HDUs till date of discharge
Supplemental Oxygen Requirement from Baseline15 daysDuration of increased supplemental oxygen requirement from baseline
Radiological outcome15 daysFollow up radiological response HR-CT.

Countries

Pakistan

Contacts

Primary ContactMuhammad Irfan Malik, FCPS
drmirfanmalik@hotmail.com03334367220
Backup ContactSardar Al-Fareed Zafar, FCPS
alfareedivf@hotmail.com03214056891

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026