Wireless EEG to predict Neurological outcome in ICU

Predicting clinical outcome in Neurosurgical ICU using quantitative uninterrupted real-time wireless EEG analysis

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

CTRI

Registry ID

CTRI/2018/10/016184

Enrollment

Registered

2018-10-29

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: S00-S09- Injuries to the head

Interventions

Control Intervention1: NIL: NIL

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients >18 years and 2. Patients admitted to the neuro ICU within 12 hours of Moderate Head Injury. Glasgow Coma Scale (GCS) 8-12, Severe Head Injury GCS

Exclusion criteria

Exclusion criteria: 1. Patients who have been subjected to a surgical procedure 2. Patients who have a planned surgical procedure within the following 6 hours at admission. 3. Patients who are extremely restless and unable to maintain the headset.

Design outcomes

Primary

Measure	Time frame
We will be performing a pilot study with 25 patients. Clinical data pertaining to heart rate, blood pressure, Glasgow coma scale (GCS) and pupillary measurements will be performed and recorded at hourly intervals as per existing protocols. Specific time-based events pertaining to clinical deterioration and other significant events (clinical improvement, death) would be identified and recorded.Timepoint: Hourly monitoring of Heart Rate, Blood Pressure, GCS, Pupillary measurement will be done for the first 48 hours of the admission of the patient.	—

Measure

Time frame

We will be performing a pilot study with 25 patients. Clinical data pertaining to heart rate, blood pressure, Glasgow coma scale (GCS) and pupillary measurements will be performed and recorded at hourly intervals as per existing protocols. Specific time-based events pertaining to clinical deterioration and other significant events (clinical improvement, death) would be identified and recorded.Timepoint: Hourly monitoring of Heart Rate, Blood Pressure, GCS, Pupillary measurement will be done for the first 48 hours of the admission of the patient.

—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactAjay Hegde

Manipal Academy of Higher Education

dr.ajayhegde@gmail.com9845876551

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026