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Completed Not applicable Interventional Results available

Stereotactic Laser Ablation for Temporal Lobe Epilepsy (Slate)

ClinicalTrials.gov ID: NCT02844465

Public ClinicalTrials.gov record NCT02844465. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 5:57 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Stereotactic Laser Ablation for Temporal Lobe Epilepsy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The study is designed to evaluate the safety and efficacy of the Visualase MRI-guided laser ablation system for mesial temporal epilepsy (MTLE).

Study identification

NCT ID
NCT02844465
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
MedtronicNeuro
Industry
Enrollment
167 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2016 (Actual)
Primary completion
Dec 11, 2023 (Actual)
Completion
Dec 11, 2023 (Actual)
Last update posted
Jan 17, 2025

2016 – 2023

United States locations

U.S. sites
23
U.S. states
20
U.S. cities
23
Facility City State ZIP Site status
Hoag Memorial Hospital Presbyterian Newport Beach California 92688 —
Stanford University Palo Alto California 94305 —
University of California, San Francisco San Francisco California 94143 —
University of Colorado Anschutz Medical Campus Aurora Colorado 80045 —
University of Miami Miami Florida 33136 —
Emory University Atlanta Georgia 30322 —
University of Chicago Chicago Illinois 60637 —
Indiana University Indianapolis Indiana 46202 —
University of Louisville Hospital Louisville Kentucky 40202 —
Johns Hopkins University Baltimore Maryland 21287 —
Henry Ford Health System Detroit Michigan 48202 —
Mayo Clinic Rochester Minnesota 55905 —
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03766 —
Rutgers University - Robert Wood Johnson Medical School New Brunswick New Jersey 08901 —
Northwell Health Great Neck New York 11021 —
Columbia University Medical Center New York New York 10032 —
Wake Forest Baptist Health Winston-Salem North Carolina 27157 —
Ohio Health Research Institute Columbus Ohio 43214 —
Oregon Health & University Science Portland Oregon 97239 —
Thomas Jefferson University Philadelphia Pennsylvania 19107 —
The University of Texas Health Science Center at Houston Houston Texas 77030 —
University of Virginia Charlottesville Virginia 22903 —
University of Washington Harborview Seattle Washington 98104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02844465, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 17, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02844465 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →