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Clinical Trials/NCT03455413
NCT03455413
Completed
Not Applicable

Electrical Impedance Tomography (EIT) in Assessing the Quality of Perioperative Invasive Ventilation in PICU

University of Oulu1 site in 1 country20 target enrollmentAugust 3, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Invasive Ventilation
Sponsor
University of Oulu
Enrollment
20
Locations
1
Primary Endpoint
Silent spacies
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This is purely observational study in which quality of invasive ventilation is observed with electrical impedance tomography (EIT) during perioperative intensive care. EIT parameters will be used to assess if protective ventilation strategies are successfully followed during routine care.

Detailed Description

20 neonates and infants undergoing elective surgery and requiring postoperative treatment and follow up in PICU or in pediatric anestesiology clinic, will be included in this prospective observational study. Swisstom BB2-monitor and NeoSensorBelts will be used to monitor their ventilatory care from arrival to the operation room (prior intubation) to postoperative intensive care (until 2 hours after extubation). EIT parameters assessing lung aeration and ventilation distribution will be used to assess the quality of invasive ventilation.

Registry
clinicaltrials.gov
Start Date
August 3, 2018
End Date
October 6, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Written informed consent from a parent of legal guardian
  • Infant undergoing elective or semi-elective surgery
  • Postoperative admission to PICU expected
  • Spontaneous breathing prior to study inclusion

Exclusion Criteria

  • Need for respiratory support prior to surgery
  • Thoracic surgery
  • Body weight \< 1500g or \> 10 kg

Outcomes

Primary Outcomes

Silent spacies

Time Frame: 24 hours

Amount of silent spaces observed in different phases of treatment in comparison to baseline

Secondary Outcomes

  • Ventilation distribution(24 hours)
  • Effect of interventions on ventilatory parameters(24 hours)

Study Sites (1)

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