Clinical Trials Directory

Trials / Completed

CompletedNCT05237622

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
University of Zurich · Academic / Other
Sex
All
Age
73 Hours
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEHigh FlowStandard HighFlow therapy after weaning from continuous positive airway pressure therapy will be applied on different flow levels. Starting with a flow level of 8l/min, the flow-rates will be changed every 30 minutes subsequently from 8-6-4-2-4-6-8 l/min. Meanwhile, data on lung volume changes will be measured using electrical impedance tomography.

Timeline

Start date
2022-02-19
Primary completion
2023-01-13
Completion
2023-01-13
First posted
2022-02-14
Last updated
2024-07-09

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT05237622. Inclusion in this directory is not an endorsement.