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NCT06443970 · ClinicalTrials.gov registry record · NA
Low and High Flow Suctioning in Intubated Infants
A NA study of Respiratory Failure, sponsored by Columbia University.
- Recruiting
- Registry status
- NA
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT06443970 is a NA study of Respiratory Failure that is actively recruiting participants, run by Columbia University. The registered enrollment target is 30 participants, below the 4,523-participant average among 40 other Respiratory Failure trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06443970, a NA study of Respiratory Failure, is actively recruiting participants, sponsored by Columbia University.
- RECRUITING
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- DEVICE Exsalta Suction Device
Study Locations (1)
New York
- Columbia University - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2024-09-04 |
| Est. Completion | 2025-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06443970
The ClinicalTrials.gov registry entry for NCT06443970 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,523-participant average among 40 other Respiratory Failure trials with a reported enrollment target (99% lower). The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Respiratory Failure appearing as the primary indexed condition, and to 1 intervention - of which Exsalta Suction Device is the first listed.
NCT06443970 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT06443970 about?
NCT06443970 is a clinical study titled "Low and High Flow Suctioning in Intubated Infants". 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 oxyge...
What is the current status of trial NCT06443970?
This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2024-09-04. Estimated completion is 2025-12-31.
What conditions does trial NCT06443970 study?
This clinical trial studies the following conditions: Respiratory Failure.
What interventions are being tested in trial NCT06443970?
The interventions under investigation include: Exsalta Suction Device (DEVICE).
Who is sponsoring clinical trial NCT06443970?
This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06443970 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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