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n-CPAP Versus n-BiPAP and NIPPV for Postextubation in RDS in Preterms

Respiratory Distress Syndrome Clinical Trial

Official title:
Non-invasive Ventilation as a Post Extubation Mode for RDS: a Randomized, Cotrolled Trial to Compare n-CPAP by n- Bipap and NIPPV

Clinical Trial Summary

non-invasive ventilation in preterms complaining from RDS a randomized, controlled trial to compare between capap, n-bipap and NIPPV

Clinical Trial Description

The primary aim of this study is to compare the impact of early extubation to nasal continuous positive airway pressure (n-CPAP) versus nasal Bilevel positive airway pressure (n-BiPAP) and non invasive positive pressure ventilation(NIPPV) on the need for mechanical ventilation via endotracheal tube (MVET) to 7 days of age or less in preterm infants less than or equal to 34 weeks' gestation requiring intubation and surfactant if indicated for respiratory distress syndrome within 120 min of delivery . Second aim is to compare different outcomes of post-extubation n-CPAP , n-BiPAPand NIPPV. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01770925
Study type Interventional
Source Ain Shams University
Contact
Status Completed
Phase N/A
Start date May 1, 2017
Completion date May 1, 2019
View Details
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