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

Respiratory Failure Clinical Trial

Official title:
Ventilator Induced Diaphragm Dysfunction in Pediatric Critically Ill Patients

Clinical Trial Summary

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

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03768232
Study type Observational
Source Bambino Gesù Hospital and Research Institute
Contact
Status Not yet recruiting
Phase
Start date January 1, 2019
Completion date January 1, 2020
View Details
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