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Functional Residual Capacity During Different Levels of High-flow in Preterm Infants — FUNK-FLOW  

Respiratory Distress Syndrome Clinical Trial

Official title:
The FUNK-FLOW Study - Functional Residual Capacity During Different Levels of High-flow in Preterm Infants

Clinical Trial Summary

Although there is a widespread use of HighFlow therapy around the world, there is still uncertainty about the most appropriate initial HighFlow level after nasal continuous positive airway pressure therapy. Higher levels might produce excessive and harmful intra-alveolar pressures exceeding those reached during nasal continuous positive airway pressure therapy. Low levels may not generate sufficient distending pressures, which may result in a loss of functional residual capacity and an increased risk of respiratory failure. Therefore, the aim of this study is to assess the effect of different HighFlow levels on the functional residual capacity and to compare these findings to the functional residual capacity during nasal continuous positive airway pressure therapy.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05237622
Study type Interventional
Source University of Zurich
Contact
Status Completed
Phase N/A
Start date February 19, 2022
Completion date January 13, 2023
View Details
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