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Heart Rate Variability in Children With Traumatic Brain Injury (HRV-TBI)

S

St. Justine's Hospital

Status

Completed

Conditions

Traumatic Brain Injury
Child Development

Treatments

Diagnostic Test: HRV monitoring

Study type

Observational

Funder types

Other

Identifiers

NCT03701620
HSJ 2018-1575

Details and patient eligibility

About

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.

Full 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.

Enrollment

15 patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • <18 years
  • admitted to the PICU at the CHUSJ
  • moderate TBI (Glasgow Coma Scale (GCS): 9-12) or severe TBI (GCS ≤8) as - - assessed 30 minutes after TBI or upon arrival in the emergency room
  • written parental consent.

Exclusion criteria

  • children fulfilling brain death criteria at the time of PICU admission (GCS 3 and loss of all brain stem reflexes)
  • children with a pacemaker or with previously diagnosed arrhythmia (HRV monitoring not reliable)
  • inflicted trauma (different underlying pathophysiology)
  • patients or parents who do not speak or read English or French.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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