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Heart Rate Variability in Children With Traumatic Brain Injury

NCT03701620 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2021-10-06

No results posted yet for this study

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.

Conditions

Interventions

DIAGNOSTIC_TEST

HRV monitoring

HRV monitoring derived from electrocardiogram

Sponsors & Collaborators

  • St. Justine's Hospital

    lead OTHER

Eligibility

Min Age
0 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2019-07-05
Completion
2021-02-10

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03701620 on ClinicalTrials.gov