Clinical Trials Directory

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UnknownNCT03768232

Ventilator Induced Diaphragm Dysfunction in Pediatric Critically Ill Patients (VIDD)

Ventilator Induced Diaphragm Dysfunction in Pediatric Critically Ill Patients

Status
Unknown
Phase
Study type
Observational
Enrollment
80 (estimated)
Sponsor
Bambino Gesù Hospital and Research Institute · Academic / Other
Sex
All
Age
28 Days – 18 Years
Healthy volunteers
Not accepted

Summary

evaluation of diaphragmatic disfunction eventually occurred in pediatric patient undergoing mechanical ventilation therapy

Detailed description

Physician will perform US diaphragm measurements within 36 hours of initiation of MV. Measurements will be repeated daily for the duration of MV for the first week, then every 48 hours and 24 hours after the extubation. Exposure to and duration of continuous NMBA infusion during the course of MV and use of CS will be recorded. Ventilator logs and arterial gas analysis will be checked at the time of each US measurement to ascertain ventilator settings and SBF for the 24 hours preceding each US measurement. Extubation success will be defined as no requirement for reintubation within 48 hours following extubation. The use of NIV immediately after extubation will be decided by the physician in charge according to the patient clinical history (presence of withdrawal syndrome, ect) and NOT according to DTF measurement.

Conditions

Interventions

TypeNameDescription
OTHERultrasound asessmentUS diaphragm measurements within 36 hours of initiation of MV. Measurements will be repeated daily for the duration of MV for the first week, then every 48 hours and 24 hours after the extubation.

Timeline

Start date
2019-01-01
Primary completion
2020-01-01
Completion
2020-01-01
First posted
2018-12-07
Last updated
2018-12-07

Source: ClinicalTrials.gov record NCT03768232. Inclusion in this directory is not an endorsement.