Empirical Mode Decomposition in the Electroencephalogram

June 4, 2020 updated by: National Taiwan University Hospital

Empirical Mode Decomposition in the Electroencephalogram During General Anesthesia Between Generations

Bispectral index (BIS), a standard monitor for perioperative monitor of patient's conscious level, is a noninvasive medical technique for monitoring and recording the electrical activity of brain.

Study Overview

Status

Completed

Conditions

Detailed Description

The electroencephalogram and BIS data have lots of information. Fourier transformation to decompose EEG was first applied on the EEG signaling until now. The disadvantages of Fourier transformation is hard to deal with physical signals, which was modulated by autonomic system and factors. The Hilbert-Huang transform (HHT) was proposed to decompose EEG signal into intrinsic mode functions (IMF) since 2004. HHT can obtain instantaneous frequency data and work well for data that is nonstationary and nonlinear. HHT have been applied for wild ranges, not only in the analysis of arrhythmia for medical and public health fields, but also in the earthquake detection and earth physics detection…etc.

The relationship between frontal EEG patterns and general anesthesia remain poorly understood. It can only say that the increase in frontal EEG power and shift power to lower frequencies during general anesthesia from publications. The investigators are going to compare the EEG signal between generations, try to find the difference in aging using empirical mode decomposition method.

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan, 100
        • Feng-Fang Tsai

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

20-40y/o patients or over 60y/o patients without severe systemic disease who were scheduled for general anesthesia.

Description

Inclusion Criteria:

  1. 20-40y/o or over 60y/o
  2. Scheduled for low risk general anesthesia
  3. Suitable for surgery after interviewed by anesthesiologist

Exclusion Criteria:

  1. Not suitable for general anesthesia
  2. High risk patient
  3. Allergic to the EEG sensor

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Younger
20-40 years old patients
Elderly
over 60 years old patients

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
EEG power calculation
Time Frame: During the operation time.
The investigator use root mean square energy to calculate EEG power.
During the operation time.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Feng-Fang Tsai, MD, National Taiwan University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 15, 2016

Primary Completion (Actual)

June 15, 2019

Study Completion (Actual)

June 15, 2019

Study Registration Dates

First Submitted

December 1, 2015

First Submitted That Met QC Criteria

October 4, 2017

First Posted (Actual)

October 6, 2017

Study Record Updates

Last Update Posted (Actual)

June 5, 2020

Last Update Submitted That Met QC Criteria

June 4, 2020

Last Verified

April 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 201508007RIN

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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