Clinical Trials Directory

Trials / Completed

CompletedNCT04441736

Post -Extubation Respiratory Failure

Different Oxygenation Modalities for Early Post Extubation Failure

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

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-intubation rate, ICU outcome \& 28 days mortality

Detailed description

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

Conditions

Interventions

TypeNameDescription
DEVICEHigh flow nasal cannulaDevice gives high flow oxygen comparable to non invasive ventilation and conventional oxygen therapy

Timeline

Start date
2019-02-20
Primary completion
2020-05-30
Completion
2020-05-31
First posted
2020-06-22
Last updated
2024-05-31

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04441736. Inclusion in this directory is not an endorsement.