Other Clinical Trial - Physiological Changes With High-Flow Nasal Cannula

Status Completed

Clinical Trial Summary

To measure changes in physiologic parameters in extremely low birthweight (ELBW) infants on high-flow nasal cannula compared to nasal continuous positive airway pressure (nCPAP).

Clinical Trial Description

After informed consent is obtained, eligible infants who are stable on nCPAP therapy of 5-7 cm H20 achieved with a ventilator, an underwater "bubble" system, or a variable-flow device will be enrolled. All subjects will have physiologic data and electrical impedance tomography collected at: 1. Baseline nCPAP for 15 minutes 2. Upon transition to high flow nasal cannula at 8 LPM for 6 hours. Data collection is obtained after infant is calm for 15 minutes at the beginning and end of this 6 hour period 3. Then upon return to baseline NCPAP for a final 15 minutes of data collection. ;

Study Design

Related Conditions & MeSH terms

Respiratory Distress Syndrome
Respiratory Distress Syndrome in Premature Infant
Respiratory Distress Syndrome, Newborn

Clinical Trial Details

NCT number	NCT03700606
Study type	Interventional
Source	Sharp HealthCare
Contact
Status	Completed
Phase	N/A
Start date	March 15, 2019
Completion date	February 14, 2022

View Details

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