A Deep Learning Framework for Pediatric TLE Detection Using 18F-FDG-PET Imaging

Symmetricity-Driven Learning Framework for Pediatric Temporal Lobe Epilepsy Detection Using 18F-FDG-PET Imaging

This study aims to use radiomics analysis and deep learning approaches for seizure focus detection in pediatric patients with temporal lobe epilepsy (TLE). Ten positron emission tomograph (PET) radiomics features related to pediatric temporal bole epilepsy are extracted and modelled, and the Siamese network is trained to automatically locate epileptogenic zones for assistance of diagnosis.

Study Overview

Status

Completed

Detailed Description

Purpose:The key to successful epilepsy control involves locating epileptogenic focus before treatment. 18F-FDG PET has been considered as a powerful neuroimaging technology used by physicians to assess patients for epilepsy. However, imaging quality, viewing angles, and experiences may easily degrade the consistency in epilepsy diagnosis. In this work, the investigators develop a framework that combines radiomics analysis and deep learning techniques to a computer-assisted diagnosis (CAD) method to detect epileptic foci of pediatric patients with temporal lobe epilepsy (TLE) using PET images.

Methods:Ten PET radiomics features related to pediatric temporal bole epilepsy are first extracted and modelled. Then a neural network called Siamese network is trained to quanti-fy the asymmetricity and automatically locate epileptic focus for diagnosis.The performance of the proposed framework was tested and compared with both the state-of-art clinician software tool and human physicians with different levels of experiences to validate the accuracy and consistency.

Study Type

Observational

Enrollment (Actual)

201

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

    • Zhejiang
      • Hangzhou, Zhejiang, China, 310009
        • Department of Nuclear Medicine and PET/CT Center, The Second Affiliated Hospital, School of Medicine, Zhejiang University

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

6 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Pediatric patients with Temporal Lobe Epilepsy

Description

Inclusion Criteria:

  1. Clinical diagnosis of temporal lobe epilepsy.
  2. Age range from six to eighteen years old.
  3. Underwent PET, EEG, computed tomography (CT) and MRI.

Exclusion Criteria:

  1. Image quality is unsatisfactory (e.g. severe image artifacts due to head movement).
  2. 18F-FDG PEG examination is negative.
  3. Clinical data is incomplete.
  4. EEG or MRI report is missing.

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

  • Observational Models: Cohort
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Experimental Group
The experimental group received 18F-FDG PET examination
Control Group
The control group received 18F-FDG PET examination

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The 'area under curve' (AUC ) of our model in detection performance
Time Frame: Through study completion, about 1 year
To evaluate the performance of our model, the investigators calculated the AUC of our model for normal or abnormal classification campared with different methods and and physicians with different levels.
Through study completion, about 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The 'dice similarity coefficient' (DSC) of our model in detection performance
Time Frame: Through study completion, about 3 months
The accuracy of focus lesion detection is quantitatively measured through the metric of 'dice similarity coefficient' (DSC) by comparing the spatial overlap between the marked regions between the reference standard and the subject method under test.
Through study completion, about 3 months

Collaborators and Investigators

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

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.

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)

June 1, 2018

Primary Completion (Actual)

February 28, 2019

Study Completion (Actual)

April 30, 2019

Study Registration Dates

First Submitted

November 13, 2019

First Submitted That Met QC Criteria

November 17, 2019

First Posted (Actual)

November 20, 2019

Study Record Updates

Last Update Posted (Actual)

January 2, 2020

Last Update Submitted That Met QC Criteria

December 30, 2019

Last Verified

June 1, 2019

More Information

Terms related to this study

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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