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High Flow Nasal Therapy in Covid 19 Patient

Predictors of Success of High Flow Nasal Therapy in Covid 19 Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05094648
Enrollment
60
Registered
2021-10-26
Start date
2021-11-01
Completion date
2022-09-30
Last updated
2021-10-26

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

Conditions

High Flow Nasal Therapy

Brief summary

This study aims to To identify factors that predict success of high flow nasal therapy in covid19 patients .

Detailed description

Coronavirus disease 2019 (COVID-19) is a potentially fatal infection caused by the novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2)\[1\]. The highly contagious nature and exponential spread of SARS-CoV-2, coupled with its potential for a rapid progressto acute respiratory distress syndrome (ARDS), has overwhelmed health care systems globally, contributing to the high mortality rates in early reports \[1,2\]. The initial approach for respiratory support for severe COVID-19 pneumonia centredaround invasive mechanical ventilation and the standard lung protective strategy recommended for ARDS\[3\]. This may have been detrimental to a proportion of patients due to ventilator induced lung injury (VILI) and associated systemic inflammation\[4\]. Furthermore, other strategies to improve oxygenation may be more appropriate in patients with hypoxemic respiratory failure who do not require ventilatorysupport\[4\]. High-flow nasal oxygen (HFNO) is delivered by an air/oxygen blender, an active humidifier, a single heated circuit, and a nasal interface. It delivers adequately heated and humidified medical gas at flow-rates of up to 60L/min, and is considered to have a number of physiological benefits, including the reduction of anatomical dead space and work of breathing, the provision of a constant fraction of inspired oxygen with adequate humidification and a degree of positive end-expiratory pressure (PEEP) \[5,6\].

Interventions

effect of high flow nasal therapy in covid 19 patients who pass and who need non invasive

Sponsors

Maha Mahmoud Ahmed
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* All Patients above 18 y old that will be diagnosed as COVID 19 based on PCR testing, who fulfil criteria that indicate need for high flow nasal therapy.

Exclusion criteria

* o Children less than 18 y old * Oropharyngeal and Nasopharyngeal swap negative patients * Patients who will refuse inclusion in the study

Design outcomes

Primary

MeasureTime frameDescription
predictors of success of high flow nasal therapy in covid 19 patientsBaselineThis study aims to To identify factors that predict success of high flow nasal therapy in covid19 patients

Contacts

Primary ContactMaha Mahmoud
maha.mahmoud.1994@gmail.com01063453193
Backup Contactsamiaa sadik
samiaa_sadek@yahoo.com01006769597

Outcome results

None listed

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