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UnknownNCT03877354

Comparison of Tidal Volume Between Pediatric Anaesthesia and Paediatric Intensive Care Patients

Comparison of Tidal Volume Between Pediatric Anaesthesia and Paediatric Intensive Care Patients: Retrospective Study

Status
Unknown
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Brno University Hospital · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

Paediatric anaesthesiology and paediatric intensive care unit data will be retrospectively screened for the data regarding mechanical ventilation. The primary aim will be the tidal volume setting and the secondary the level of positive end-expiration pressure (PEEP) according to the inspired oxygen fraction (FIO2), and the level of driving pressure.

Detailed description

Protective positive pressure ventilation (tidal volume ≤6 mL/kg) in adult patients in intensive care is currently considered as a standard procedure. It is associated with a reduction of morbidity and positive outcome. In paediatric patients there are available only limited information related to the size of the tidal volume and it is recommended to use the volume between 5 and 8 mL per kg for the whole spectrum of ages of pediatric patients. The aim of this retrospective observational study is to evaluate the tidal volumes used in clinical practice in pediatric patients during general anesthesia and compared it to the tidal volumes used in paediatric critical care. Data will be harvested from the anaesthesiology records and from the paediatric intensive care unit charts. The tidal volume will calculated per kg of actual weight.

Conditions

Interventions

TypeNameDescription
OTHERData from anaesthesia records for ventilation setting screeningData from anaesthesia records will be retrospectively screened for the ventilation settings
OTHERData from intensive care records for ventilation setting screeningData from paediatric intensive care charts will be retrospectively screened for the ventilation settings

Timeline

Start date
2019-04-01
Primary completion
2023-12-31
Completion
2023-12-31
First posted
2019-03-15
Last updated
2023-07-27

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT03877354. Inclusion in this directory is not an endorsement.