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Post -Extubation Respiratory Failure | Clinical Trials | Clareo Health

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COMPLETEDNANCT04441736

Post -Extubation Respiratory Failure

comparing high flow nasal cannula , conventional oxygen tharapy and non invasive ventilation post-extubation period for patients mechanically ventilated due to respiratory failure regarding re-intubat...

Lead sponsor: Cairo University•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Cairo University

patients with respiratory failure either type I or type II planned for extubation will be divided into 3 groups post extubation : Group I: will receive high flow nasal cannula giving oxygen 60 litres / minute flow group II: will receive nasal cannula up to 10 litres / minute group III: will receive non invasive ventilation Data of the patients will be collected for 28 days post-extubation and analysed

Age

18 - 80 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•respiratory failure type I and Type II

Exclusion Criteria

•Mechanical ventilation due to other cause such as disturbed conscious level or respiratory muscle weakness

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: May 31, 2024Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment60

Start dateFeb 2019

Last updatedMay 31, 2024

Condition

Respiratory Insufficiency

Locations shown

Faculty of Medicine

Giza

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 31, 2024Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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