Skip to main content
Clinical Trials/NCT02846272
NCT02846272
Recruiting
Not Applicable

Diffusion Tensor and Functional Connectivity Imaging in Pediatric Epilepsy: Imaging/Histology Correlation

The University of Texas Health Science Center, Houston1 site in 1 country50 target enrollmentNovember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intractable Epilepsy
Sponsor
The University of Texas Health Science Center, Houston
Enrollment
50
Locations
1
Primary Endpoint
Number of participants with seizure outcome as determined by Engel
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

To determine the utility of diffusion tensor magnetic resonance imaging in the preoperative workup of children with intractable epilepsy referred for surgery.

Detailed Description

To determine if diffusion tensor and functional connectivity magnetic resonance imaging helpful to better understand and diagnose intractable epilepsy in children. All enrolled children will undergo standard preoperative and postoperative MRI imaging, plus a 15 minute set of functional connectivity and diffusion tensor sequence with no additional sedation. This imaging data will be stripped of identifiers and be processed to provide both quantitative analysis, resting state functional connectivity changes and three dimensional modeling of white matter tracts adjacent to epileptogenic foci. This study is being done to determine if diffusion tensor and functional connectivity magnetic resonance imaging are helpful to better understand and diagnose intractable epilepsy in children.

Registry
clinicaltrials.gov
Start Date
November 2015
End Date
January 1, 2031
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Manish Narendra Shah

M.D. , Assistant Professor

The University of Texas Health Science Center, Houston

Eligibility Criteria

Inclusion Criteria

  • Children diagnosis with Intractable Epilepsy

Exclusion Criteria

  • No Intractable Epilepsy

Outcomes

Primary Outcomes

Number of participants with seizure outcome as determined by Engel

Time Frame: 5 years

Study Sites (1)

Loading locations...

Similar Trials