Association Between qEEG Measure and Post-Operative Cognitive Dysfunction (POCD) and Postoperative Delirium (POD)

A Blind, Observational, Prospective, Multi -Center, One Arm, Study on the Association Between qEEG Measure and Post-Operative Cognitive Dysfunction (POCD) and Postoperative Delirium (POD)

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03977350

Enrollment

Registered

2019-06-06

Start date

2019-09-23

Completion date

2022-12-01

Last updated

2020-09-11

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

Conditions

Cognitive Dysfunction

Brief summary

Cognitive complications after major surgery are a common phenomenon. The incidence of Postoperative Cognitive Dysfunction (POCD), may vary from 5% to 25% in adult patients, depending on different risk factors. Age has been strongly associated with cognitive complications. POCD is a prolonged decline in cognitive function that appears after surgery as compared with preoperative functions. In order to classify evaluate POCD, it requires at least 2 measurements. A baseline, completed before surgery and a second measurement, post surgery. In light of the high prevalence of POCD and the difficulties in its prediction, NeuroIndex has developed a quantitative EEG system and software that aim to produces risk predictor index (IS) for POCD. This study aims to evaluate the relationship between the software produced predictor index and the actual POCD events. The qEEG will be monitored during the surgery in addition to the routine clinical practice in operating rooms. POCD will be evaluated using Montreal Cognitive Assessment test (MoCA) prior and post surgery.

Interventions

DEVICEEEG monitoring

EEG monitoring under general anesthesia

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

65 Years to No maximum

Healthy volunteers

Inclusion criteria

* Males and females between the ages of 65 or above. * Subjects with American Society of Anesthesiologists physical status I-III. * Subjects who are intended to undergo cardiac surgery (CABG or valve replacement) under general anesthesia. * Surgical procedures scheduled for over 30 minutes. * Lack of significant hearing disturbances. * Subjects with ability to read and understand the consent form.

Exclusion criteria

* Significant visual impairment so that the pictures of the confusion assessment method could not be interpreted to accurately test to assess delirium. * Profound dementia or aphasia that interfered with the assessment of cognitive dysfunction (positive delirium in CAM-ICU). * Patients with a history of stroke. * Any documented major neurologic or psychiatric dysfunction. * Pregnant women. * Long term use of sedative-hypnotic drugs and antidepressant drug. * Subjects with scalp or skull abnormalities (s/p brain surgery, cranial implants).

Design outcomes

Primary

Measure	Time frame	Description
The qEEG parameter IS correlation with POCD	1 week following surgery	The qEEG parameter IS, which range between 0 and 1, where higher scores are more favorable than lower scores will be evaluated for its correlation with POCD that will be measured by Montreal Cognitive Assessment (MoCA)

Countries

Israel

Contacts

Primary ContactEster Pri-Or, Nurse CRA

Ester@neuroindex.com972-506629699

Backup ContactTamar A Arens, Dr.

Tamar@neuroindex.com972543532120

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026