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Clinical Trials in Australia / NCT07585643
Starting soon Observational

IBIS - Investigating Reliability of BIS and SEDLINE Monitoring in Children With Developmental and Epileptic Encephalopathies (DEE).

NCT07585643 · tracked via the Priya Life Science Australia tracker
Phase
Observational
Started
2026-09-03
Last updated
2026-07-17

Condition(s) studied

Epileptic EncephalopathyEarly Infantile Epileptic EncephalopathyInfantile SpasmDevelopmental and Epileptic Encephalopathies

Investigational drug(s) / intervention(s)

Monitoring of patients using electroencephalogram, a Bispectral Index (BIS) and Sedline monitors.

Monitoring of patients using electroencephalogram, a Bispectral Index (BIS) and Sedline monitors.: This is an observational study of children under 16 years of age, who will be fitted with a 21-lead EEG and then, in consecutive random order, a BIS or Sedline monitor with measurements taken for 30 minutes with each monitor, 60 min in total. This will allow pEEG data to be measured against a corresponding continuous EEG. The depth of anaesthesia monitors used are Bispectral Index (BIS, Medtronic, Minneapolis, Minnesota, USA) and Sedline (Masimo, Irvine, California, USA).

Study summary

When children have surgery, anaesthetists carefully monitor the depth of anaesthesia by using sensors on the forehead that measure brain activity, also known as processed electroencephalogram (pEEG). These monitors are routinely used in paediatric anaesthesia; however, investigators do not know if they work accurately in babies and young children with seizure disorders or on anti-seizure medications.

Children with developmental and epileptic encephalopathies may need anaesthesia for tests or procedures. It is important that their treating doctors understand whether these monitors truly reflect how awake or asleep the children are. This study aims to compare a child's electrical brain activity using two commonly used devices in paediatric anaesthesia with the conventional 21-lead EEG patterns in children with seizure disorders. The results of this research may help improve the safety and perioperative care of children with seizure disorders who require general anaesthesia in the future.

Eligibility

Sex
ALL
Min age
0 Years
Max age
15 Years
Healthy volunteers
No
Inclusion Criteria: * Children (\<16 years old) with a confirmed diagnosis of early onset EE or DEE due to any cause (prior to age 2 years). Exclusion Criteria: * Language barriers impeding data collection * Department for Child Protection and Family Support is involved in the care of the child.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Perth Children's Hospital Perth Western Australia
Hospital das Clinicas, São Paulo, Sao Paulo São Paulo Brazil

More Telethon Kids Institute trials in Australia

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07585643 on ClinicalTrials.gov ↗ ← All trials in Australia