Skip to content

Optimal High CPAP Pressures in Preterm Neonates Post-extubation

Optimal High CPAP Pressures in Preterm Neonates Post-extubation: A Prospective Randomized Crossover Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05230485
Enrollment
26
Registered
2022-02-09
Start date
2022-02-15
Completion date
2024-02-15
Last updated
2022-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mechanical Ventilation Complication, Preterm Birth, Respiratory Distress Syndrome, Newborn

Keywords

Continuous Positive Airway Pressure, Electrical activity of diaphragm, Continuous distending pressure

Brief summary

Use of continuous positive airway pressure (CPAP) in preterm neonates has traditionally been limited to between 5-8 cmH2O. In recent years, use of CPAP pressures ≥9 cmH2O is becoming more common in neonates with evolving chronic lung disease, in lieu of other non-invasive modes or invasive mechanical ventilation. A particular knowledge gap in the current literature is the choice of the level of pressure level when using High CPAP as a post-extubation support mode. In this study, we will comparatively evaluate the short-term impact of two different high CPAP pressures when used as a post-extubation support mode in preterm neonates.

Detailed description

Background: Use of continuous positive airway pressure (CPAP) in preterm neonates has traditionally been limited to between 5-8 cmH2O. In recent years, use of CPAP pressures ≥9 cmH2O is becoming more common in neonates with evolving chronic lung disease, in lieu of other non-invasive modes or invasive mechanical ventilation. However, there are limited data on the effectiveness and safety of this mode. A particular knowledge gap in the current literature is the choice of the level of pressure level when using High CPAP as a post-extubation support mode. While it could be argued that the initial High CPAP pressure post-extubation should be somewhat higher than the pre-extubation mean airway pressure (Paw), there remain concerns of potential complications as well as uncertainty around degree of leak and resulting effectiveness. On the other hand, a suboptimal post-extubation High CPAP level may lead to atelectasis and contribute towards extubation failure, potentially prolonging invasive ventilation and associated risks. As such, research towards identification of the optimal High CPAP level post-extubation from high invasive ventilation pressures is warranted. Objective: To comparatively evaluate the short-term impact of two different high CPAP pressures when used as a post-extubation support mode in preterm neonates. Hypothesis: We hypothesize that babies extubated from invasive mechanical ventilation with a mean Paw between 9-15 cmH2O will demonstrate better physiological and clinical parameters when using High CPAP+2 cmH2O vs equivalent CPAP levels. Methods: Design - This will be a prospective, single-centre, randomized cross-over study.

Interventions

The level of continuous distending pressure (or positive end-expiratory pressure) chosen on CPAP

Sponsors

McMaster Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Days to 37 Weeks
Healthy volunteers
No

Inclusion criteria

* Gestational age \<29 weeks; chronological age \>7 days; post-menstrual age \<37 weeks; extubation from invasive ventilation with measured mean airway pressure 9-15 cmH2O

Exclusion criteria

* Any congenital or genetic/chromosomal abnormality

Design outcomes

Primary

MeasureTime frameDescription
Peak Edi60 min following each CPAP level - assessed over 10 minThe peak electrical diaphragmatic activity - a surrogate for work of breathing to generate tidal volume

Secondary

MeasureTime frameDescription
Regional cerebral perfusion60 min following each CPAP level - assessed over 10 minThe cerebral tissue extraction of oxygen - determined by near infra-red spectroscopy
Pressure level - Ventilator60 min following each CPAP level - assessed over 10 minPressure level as measured by the ventilator
Pressure level - Interface60 min following each CPAP level - assessed over 10 minPressure level at measured at the nasal interface used to deliver CPAP
Work of breathing scoreOver entire duration (70 min) at each CPAP level, assessed every 10 minUsing Silverman Scoring
Heart RateOver entire duration (70 min) at each CPAP level, assessed every 10 minFrom cardiorespiratory monitoring
Minimum EDi60 min following each CPAP level - assessed over 10 minThe minimum eelectrical diaphragmatic activity - a surrogate for work of breathing to maintain functional residual capacity
Transcutaneous CO2 levelOver entire duration (70 min) at each CPAP level, assessed every 10 minFrom bedside transcutaneous CO2 monitoring
FiO2 levelOver entire duration (70 min) at each CPAP level, assessed every 10 minFractional inspired oxygen level, as determined by clinical and inputted into ventilator
Number of bradycardic episodes <80 bpmOver entire duration (70 min) at each CPAP levelas above
Proportion of duration with SpO2 <90%Over entire duration (70 min) at each CPAP levelduration of time where the patient's SpO2 is less than 90%
Respiratory RateOver entire duration (70 min) at each CPAP level, assessed every 10 minFrom cardiorespiratory monitoring

Countries

Canada

Contacts

Primary ContactAmit Mukerji, MD
mukerji@mcmaster.ca905-521-2100

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026