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Clinical Trials/NCT03977350
NCT03977350
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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)

Neuroindex Ltd.1 site in 1 country50 target enrollmentSeptember 23, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cognitive Dysfunction
Sponsor
Neuroindex Ltd.
Enrollment
50
Locations
1
Primary Endpoint
The qEEG parameter IS correlation with POCD
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 23, 2019
End Date
December 1, 2022
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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).

Outcomes

Primary Outcomes

The qEEG parameter IS correlation with POCD

Time Frame: 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)

Study Sites (1)

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