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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02846272
Acronym
DTI/SEP
Enrollment
50
Registered
2016-07-27
Start date
2015-11-30
Completion date
2031-01-01
Last updated
2024-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intractable Epilepsy

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.

Interventions

PROCEDUREObservation

Observation of MRI changes in subjects

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
0 Days to 18 Years
Healthy volunteers
No

Inclusion criteria

* Children diagnosis with Intractable Epilepsy

Exclusion criteria

* No Intractable Epilepsy

Design outcomes

Primary

MeasureTime frame
Number of participants with seizure outcome as determined by Engel5 years

Countries

United States

Contacts

Primary ContactManish N Shah, M.D.
Manish.N.Shah@uth.tmc.edu713 500-7410
Backup ContactBangning L Yu, R.N., PhD
Bangning.Yu@uth.tmc.edu713 500-7363

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026