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EEG Abnormalities as Predictor of Outcome in Pediatric Encephalopathy

Electroencephalographic (EEG) Abnormalities as a Predictor of Poor Outcome in Pediatric Encephalopathy

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07825675
Enrollment
147
Registered
2026-09-17
Start date
2026-09-10
Completion date
2028-03-10
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Diseases, Encephalopathy

Keywords

EEG, Pediatric encephalopathy, Prognosis, PCPC, Neurological outcome, Assiut

Brief summary

This prospective cohort study aims to evaluate the prognostic value of electroencephalographic (EEG) abnormalities in predicting poor clinical outcomes among children with encephalopathy admitted to Assiut University Children Hospital.

Detailed description

Pediatric encephalopathy has multiple etiologies and variable neurological outcomes. Early prognostic assessment is essential for clinical decision-making and family counseling. Electroencephalography (EEG) is a non-invasive tool that may help predict neurological outcome. This prospective observational study will include children aged 1 month to 18 years with clinical diagnosis of encephalopathy. EEG will be performed within the first 48 hours of admission. Neurological outcome will be assessed at hospital discharge using the Pediatric Cerebral Performance Category (PCPC) scale. A PCPC score of 1-2 will be considered good outcome and a score of ≥3 will be considered poor outcome.

Interventions

None listed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

* Age from 1 month to 18 years * Clinical diagnosis of encephalopathy with altered level of consciousness * EEG performed within the first 48 hours of admission * Written informed consent from parents or legal guardians

Exclusion criteria

* Neonatal encephalopathy * Children with severe pre-existing neurological disability * Known epileptic patients * Incomplete clinical or EEG data

Design outcomes

Primary

MeasureTime frameDescription
Poor neurological outcome at hospital dischargeat 30 daysProportion of children with poor neurological outcome defined as Pediatric Cerebral Performance Category (PCPC) score ≥3 at hospital discharge.

Secondary

MeasureTime frameDescription
Frequency of EEG abnormalitiesWithin the first 48 hours of admissionProportion of children with specific EEG abnormalities (diffuse background slowing, background suppression, burst suppression, absent reactivity, low-voltage activity, or electrographic seizures) recorded within the first 48 hours of admission.
Predictive performance of EEG abnormalities for poor outcomeat 30 daysSensitivity, specificity, and predictive values of specific EEG abnormalities for poor neurological outcome (PCPC ≥3) at hospital discharge.
Mortalityat 30 daysProportion of children who die during hospital stay.
Duration of PICU stayat 30 daysLength of stay in the pediatric intensive care unit in days.

Contacts

CONTACTEsraa M Tamer, Resident
Esraa.17289969@med.aun.edu.eg+20 11 58780125
STUDY_CHAIRGamal A Asker, prof

Pediatrics Department, Assiut University Hospitals

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026