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Clinical Trial 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


Clinical Trial 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 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04441736
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date February 20, 2019
Completion date May 31, 2020

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