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Clinical Trial Summary

Using a prospective cohort of children admitted to the PICU, the investigators will determine HRV monitoring is feasible, if a decreased HRV in the 7 days following moderate or severe TBI in children is associated with a worse outcome 6 months post-TBI and investigate HRV as a tool that can predict adverse events (neurological crisis) within 2 days following TBI.


Clinical Trial Description

This is a single center prospective cohort study of 15 children <18 years, admitted to the PICU at the CHU Sainte-Justine (CHUSJ) with moderate or severe TBI (<24 hours). Neurodevelopment outcome of children will be evaluated 6 months post TBI. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03701620
Study type Observational
Source St. Justine's Hospital
Contact
Status Completed
Phase
Start date January 1, 2018
Completion date February 10, 2021

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