Ventilation of the Extremely Premature Infants Optimized by Dead Space Washout
Condition(s) studied
Investigational drug(s) / intervention(s)
Ventilation with Dead Space Washout via Continuous Tracheal Gas Insufflation (CTGI): The intervention involves adding a device which allows CTGI (the "CTGI-device") to washout the dead space in preterm mechanically ventilated infants. Dead space washout using the CTGI-device is an option added to standard ventilation, to reduce or even cancel anatomical dead space due to respiratory prostheses in intubated preterm infants.
Study summary
The Continuous Tracheal Gas Insufflation (CTGI) is a ventilation option of conventional mechanical ventilation that is used to reduce or even eliminate the dead space caused by respiratory prostheses. This objective is of particular interest in the smallest preterm infants, where the volume of anatomical dead space due to prostheses is little different from the tidal volume. The principle of this option is to continuously blow an additional flow of 0.2 L/minute at the tip of the endotracheal tube to purge expired CO2 trapped in the prostheses, to have a CO2-free volume of gas available for subsequent insufflation.
The goal of this clinical trial is to learn if Continuous Tracheal Gas Insufflation (CTGI) works to reduce ventilatory dependence in preterm infants after mechanical ventilation. It will also learn about the safety of CTGI. The main questions it aims to answer are:
* Does Continuous Tracheal Gas Insufflation (CTGI) reduce the number of days of non-invasive ventilation in extremely preterm infants who needed mechanical ventilation?
* Does Continuous Tracheal Gas Insufflation (CTGI) reduce the age at the weaning of any ventilatory support and/or oxygen supplementation.
Researchers will compare the clinical outcome of patients mechanically ventilated with the CTGI-device to the outcome of patients ventilated without the CTGI device, to see if the CTGI ventilation works to reduce ventilation dependence.
Participants will:
• Be mechanically ventilated using CTGI (if randomly assigned in the CTGI-group), for the entire endotracheal ventilation period during their stay in the neonatal intensive care unit.
Eligibility
Primary outcome measure(s)
- Cumulative duration of all periods of non-invasive ventilation — From birth to the end of hospital stay, up to maximum 45 weeks of corrected gestational age.
The cumulative duration of all periods of non-invasive ventilation, in days, starting from birth, and up to maximum 45 weeks corrected gestational age. Non-invasive ventilation includes all types of positive pressure support non-invasive ventilation and high flow nasal cannula ventilation (HFNC).
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| Centre Hospitalier Intercommunal de Creteil | Créteil | France | |
| Centre Hospitalier Universitaire de Nantes | Nantes | France | |
| Centre Hopistalier Universitaire Cochin Port Royal aphp | Paris | France | |
| Centre hospitalier Robert Debré aphp | Paris | France |
More Centre Hospitalier Intercommunal Creteil trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06334523 on ClinicalTrials.gov ↗ ← All trials in France