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RECRUITING
NCT06443970
NA

Low and High Flow Suctioning in Intubated Infants

Sponsor: Columbia University

View on ClinicalTrials.gov

Summary

Preterm and term intubuted infants in the NICU will undergo two sequential suctioning procedures: a new, FDA-approved suction device called EXSALTA (ED) and the standard conventional wall (SCW). The physiological consequences, i.e. changes in heart rate (HR), oxygen saturation (SpO2), cerebral oxygenation (C-rSO2), and cerebral fractional oxygen extraction (C-FOE) between ED and SCW ETT tracheal suctioning system in both open and closed catheter system settings will be evaluated using a randomized cross over design in preterm and term infants receiving mechanical ventilation via an ETT. This study will evaluate the hypothesis that there will be significantly lower variations in HR, SpO2, C-rSO2, and C-FOE during ETT suctioning with ED compared to SCW suctioning systems under both open and close ETT suction settings.

Official title: Physiological Consequences of Low and High Flow Endotracheal Suctioning Devices in Intubated Preterm and Term Infants

Key Details

Gender

All

Age Range

Any - 28 Days

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2024-09-04

Completion Date

2025-12-31

Last Updated

2025-06-19

Healthy Volunteers

No

Interventions

DEVICE

Exsalta Suction Device

Low flow endotracheal suction device

Locations (1)

Columbia University

New York, New York, United States