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Technology of Intracranial Pressure Estimation by Single-Channel EEG in Brain Disease

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Seoul National University

Status

Active, not recruiting

Conditions

Intracranial Pressure Increase
Brain Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT05609071
SNUEMSBDICP

Details and patient eligibility

About

If intracranial pressure can be measured non-invasively using single-channel EEG, clinicians will be able to easily monitor changes in intracranial pressure in patients with brain diseases in the clinical setting. Therefore, a more efficient treatment plan can be established and the prognosis of patients with brain disease can be expected to improve in the long term.

Full description

Study Objectives:

  1. Accuracy evaluation of single-channel EEG-based estimated intracranial pressure and actual intracranial pressure in patients with brain disease
  2. It is intended to improve the accuracy by analyzing and upgrading the correlation and concordance of the single-channel EEG-based estimated intracranial pressure compared with the actual intracranial pressure measurement of the patient.

Study design: Multi-center prospective clinical trial

The study procedure was explained to the caregiver of the patient with brain disease admitted to the emergency room or intensive care unit, who was or will be implanted with an intracranial pressure monitoring device and informed consent was obtained.

While the intracranial pressure monitoring device is being applied, EEG data and intracranial pressure data are simultaneously acquired by applying a single-channel EEG.

EEG-based intracranial pressure prediction model and actual intracranial pressure comparison analysis are conducted to evaluate the prediction model and upgrade it.

Enrollment

10 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 years or older
  • Patients have had or are planning to insert an intracranial pressure monitoring device due to brain diseases
  • Emergency room or intensive care unit of the study hospital

Exclusion criteria

  • EEG measurement is restricted due to trauma or head deformity
  • The attachment of electrodes for EEG measurement interferes with the standard treatment
  • Patients who do not agree to enroll to this study by patients or caregivers

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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