Clinical Trials Directory

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UnknownNCT01193023

Patient-ventilator Asynchrony During Mechanical Invasive Assisted-ventilation in Pediatric Patients

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
University Hospital, Geneva · Academic / Other
Sex
All
Age
4 Weeks – 12 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to document the prevalence and type of asynchronies incidence during invasive mechanical ventilation in pediatric patients breathing under pressure support. And to observe the impact of adjusting the expiratory trigger setting on asynchronies, and compare these incidences with asynchronies measured in pediatric patient breathing under NAVA system (Neurally Adjusted Ventilatory Assist).

Detailed description

Two sessions will be recorded, one in PSV, one with NAVA, delivered in a random order after being sure the infant is calm and comfortable, according to his parents and/or the nurse in charge. Criteria for initiating invasive ventilation and to start PSV will follow the usual practice guidelines of the unit. Ventilation parameters in PS will be adjusted by the clinician in charge of the patient, as usual based on clinical observation. Investigators will not interfere with ventilator settings. Ventilation will be applied via an endotracheal tube, uncuffed for the majority (if infant \< 5 years), according to commonly applied guidelines in this unit. One 15 minutes session will be recorded, after being sure the infant is calm and comfortable according to the parents and/or the nurse in charge. Then the clinician in charge of the patient will modify the ETS, first decreasing it of 10% below the initial set value, and will be recorded the following 5 minutes after stabilization and secondly increasing it of 10% above the initial set value, and will be recorded the following 5 minutes after stabilization. NAVA will be set to deliver initially the same peak pressure (comparable level of assist) than during the initial PS period. Same PEEP will be delivered in both modes. This is possible with a pre-visualization window, allowing adjustments before switching to the NAVA mode. Nava ventilation will be recorded during 20 minutes. The 2 sessions, Pressure support and Nava, will be recorded consecutively.

Conditions

Interventions

TypeNameDescription
OTHERPressure SupportVentilation under pressure support
DEVICENAVAVentilation under NAVA

Timeline

Start date
2010-06-01
Primary completion
2011-06-01
Completion
2011-06-01
First posted
2010-09-01
Last updated
2010-09-01

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT01193023. Inclusion in this directory is not an endorsement.