Efficient Automated Localization of ECoG Electrodes in CT Images Via Shape Analysis (LOC-ECOG)

September 8, 2020 updated by: Luigi Pavone, Neuromed IRCCS

People with drug epilepsy (PwE) refractory to anti-seizure medications may be evaluated for surgery. In several cases non invasive presurgical work-up is not sufficient for localization of the Epileptogenic Zone and its correct delineation requires intracranial investigations by means of intraparenchymal or subdural electrodes.The methodological approach with subdural electrodes allows to obtain electrocorticography (ECoG) covering large cortical regions and to map eloquent areas.

To delineate the seizure onset zone it is mandatory to precisely localize the electrode position on the cortical surface. Electrodes are usually recognized by processing patients' computed tomography (CT) images using simple image processing (e.g. thresholding) that isolates metal objects. However, also wires, stitches, clips and other metal objects are actually recognized and need to be removed by manual intervention. A new automated method, based on shape analysis, will be retrospectively tested in a group of subjects with refractory focal epilepsy previously investigated with subdural electrodes for diagnostic purposes to provide advanced ECoG subdural electrodes recognition. A total of 24 CT scans with a large number (> 1700) of round platinum electrodes arrays will be recruited for testing.

Study Overview

Status

Completed

Detailed Description

For people with epilepsy (PwE) refractory to anti-seizure medication sometimes the non-invasive presurgical evaluation using ElectroEncephaloGram (EEG) recorded directly from the scalp is not sufficient to delineate the epileptogenic zone and to identificate the eloquent cortex. In these cases, an invasive approach using intracranial electroencephalography (iEEG) is needed Subdural electrodes are used frequently in the presurgical evaluation of patients who are candidates for epilepsy surgery. Electrodes placed directly on the surface of the cortex provide a signal with a much higher resolution than that provided from scalp electrodes, and have a much clear view of small loci of activity which is difficult to see on the scalp.

Subdural electrodes allow not only the localization of abnormal epileptic tissue but also the localization of adjacent normal functions. Therefore, the precise anatomical localization of the electrodes on the patient's brain plays a key role in the definition of the epileptogenic zone or in the mapping of eloquent cortex.

From a clinical point of view, the accurate localization of the anatomical boundaries of the epileptogenic zone allows to exclude eloquent areas, avoid deficits to patient and minimize brain volume resection.

The localization of these electrodes is generally obtained by matching the locations of the electrodes with the brain anatomy of the patient. Commonly, a pre-implant magnetic resonance image (MRI) is co-registered to a post-implant computed tomography scan (CT) because MRI offers higher brain tissue contrast, while CT supports electrodes localization , even if CT images are affected by metal artifacts.

Various dedicated software tools that support pre-surgical evaluation are currently available as Matlab-based packages or open source softwares, also with graphical user interfaces. They mainly provide MRI-CT co-registration and offer only basic features for recognition of ECoG electrodes from CT scans. Most dedicated softwares segment the electrodes via simple image thresholding and allow manual interaction to correct the data. Manual methods are very time consuming,user-dependent and prone to inaccuracy. On the other hand, the mere CT image thresholding method is not able to recognize all the electrodes and to completely exclude other metallic objects, such as wires, tooth filings, intracranial clips, splinters, stitches, hearing aids or intracranial stents. Hence, manual intervention is often required to adjust the data. For example, the ALICE tool considers the volume of segmented clusters to identify the electrodes, but turned out to be unable to exclude other objects with comparable volumes (e.g. wire clusters).

The aim of this project is to develop a novel, robust, automated method to recognize ECoG electrodes in CT volumes. It consists of metal artifacts removal from CT volumes, identification of groups/arrays of metal objects within the skull and shape analysis of detected objects to achieve ECoG electrodes localization.The proposed approach could be easily integrated in existing tools.

Study Type

Observational

Enrollment (Actual)

24

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

    • IS
      • Pozzilli, IS, Italy, 86077
        • IRCCS Neuromed

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

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

24 people with epilepsy (PwE) refractory to anti seizure medications (ASM) who underwent epilepsy surgery at IRCCS Neuromed.

Description

Inclusion Criteria:

  • Patients implanted with subdural ECoG electrodes underwent epilepsy surgery
  • Availability of a post-operative CT scan with acceptable image quality

Exclusion Criteria:

- Patients having CT scans with low image quality

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
Drug resistant epilepsy patients
Patients with drug resistant epilepsy underwent epilepsy surgery

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Classification accuracy of a Linear Discriminant Analysis classifier in detecting electrodes
Time Frame: September 2020

A distinct database will be created for each patient, with rows corresponding to potential electrode objects within the CT volume, and composed by a collection of the extracted geometrical features and the assigned class. Two classes will be considered: "electrode" and "non-electrode". The "electrode" class is assigned to the actual electrodes, while the non-electrode class is assigned to all the other detected metal objects.

A Linear Discriminant Analysis (LDA) algorithm will be used for model training and data classification. Classification performances will be assessed by applying a 10-fold cross validation on each of the 24 patients' databases. In 10-fold cross-validation, the dataset will be randomly divided into 10 subsets of equal size, and then each subset will be tested using the classifier trained on the remaining nine subsets. Then, the obtained 10 classification accuracies will be averaged to provide an overall classification accuracy.

September 2020

Collaborators and Investigators

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

Sponsor

Collaborators

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

August 1, 2020

Primary Completion (ACTUAL)

August 25, 2020

Study Completion (ACTUAL)

September 7, 2020

Study Registration Dates

First Submitted

July 15, 2020

First Submitted That Met QC Criteria

July 20, 2020

First Posted (ACTUAL)

July 21, 2020

Study Record Updates

Last Update Posted (ACTUAL)

September 10, 2020

Last Update Submitted That Met QC Criteria

September 8, 2020

Last Verified

September 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • BIOING_01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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