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Collection of EEG recordings in patients under general anesthesia

A prospective observational study to collect EEG recordings of hospitalized patients prior and during elective surgery under general anesthesia - EEG recordings study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/11/077275
Enrollment
20
Registered
2024-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: R298- Other symptoms and signs involvingthe nervous and musculoskeletal systems

Interventions

Control Intervention1: NIL: NIL

Sponsors

Ben Gurion University of the Negev BGU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 65 years (both inclusive) 2. Both male and female 3. Patients hospitalized for elective surgery under general anaesthesia 4. General anaesthesia classified as ASA 1 to 2 in the pre anaesthesia examination

Exclusion criteria

Exclusion criteria: 1. Any injury or damage to the scalp or skull 2. Refusal or unwillingness to participate in the study 3. Use of medications such as beta-blockers that can affect heart rate and blood pressure. 4. Patients with a history of demyelinating disease or any progressive neurological disorder 5. Patient data with an active infection of the central nervous system, severe acute or chronic disease (haematological, renal, cancer, acquired immunodeficiency syndrome) 6. Patients with impaired consciousness from various reasons

Design outcomes

Primary

MeasureTime frame
Correlation of EEG recordings with the level of consciousness in patients under general anaesthesia and develop a toolTimepoint: EEG data including 5 min of baseline activity before anaesthesia and 1-3 hours of recording during anaesthesia

Secondary

MeasureTime frame
Medications during recording/ hospitalization from the medical record in hospitalization ? Reason for monitoring (presurgical, diagnosis) ? ComorbiditiesTimepoint: 5 min of baseline activity before anaesthesia and 1-3 hours of recording during anaesthesia

Countries

India

Contacts

Public ContactSravani P S L

SunSecure Clinical Research Services Pvt Ltd

dr.suresh.karri@gmail.com9739798272

Outcome results

None listed

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