Ventilation Clinical Trial
Official title:
Neurally Adjusted Ventilatory Assist (NAVA) in Pediatric Patients
The purpose of this study is to find out if NAVA-technology is better in detecting patients
own inspiratory efforts during mechanical ventilation than currently used flow-triggering in
PRVC (pressure regulated volume controlled) ventilation, and if NAVA gives real benefits for
patients or not.
The investigators study hypothesis is that NAVA-technology can detect spontaneous
inspiration more accurately than currently used methods, and thus will lead to more smooth
adaptation to mechanical ventilation in pediatric patients. The investigators expect this to
decrease the time of ventilatory support needed.
Status | Completed |
Enrollment | 170 |
Est. completion date | May 2012 |
Est. primary completion date | May 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A to 16 Years |
Eligibility |
Inclusion Criteria: - All children from term newborn (37+0 gestational week) to 16-year-old needing ventilatory care at least 30 minutes Exclusion Criteria: - Any condition that prevents feeding tube positioning. Critical ventilatory or perfusion problems. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Finland | University Hospital of Oulu | Oulu |
Lead Sponsor | Collaborator |
---|---|
University of Oulu |
Finland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Primary outcome is the duration of mechanical ventilation | 30minutes-3weeks | No | |
Secondary | Amount of sedative medication needed | 30minutes-3weeks | No |
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