Actively Recruiting
Thalamus Seizure Detection With a Deep Brain Stimulator System
Led by Mayo Clinic · Updated on 2026-03-20
5
Participants Needed
1
Research Sites
47 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to determine the feasibility of chronic ambulatory thalamus seizure detection. The sensitivity, specificity, and false alarm rate of thalamus seizure detection will be calculated using recordings from a deep brain stimulation system, assessed relative to concurrent gold-standard video-EEG monitoring collected in the in-patient setting (epilepsy monitoring unit), in 5 patients with drug resistant epilepsy.
CONDITIONS
Official Title
Thalamus Seizure Detection With a Deep Brain Stimulator System
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age and older
- Implanted with a clinical DBS system for epilepsy with brain recording capabilities (Medtronic Percept153 DBS)
- Able to understand study procedures and comply with them for the entire study duration
You will not qualify if you...
- Health conditions or status that would pose undue risk for epilepsy monitoring unit evaluation
- Women who are pregnant or test positive on urine pregnancy test if applicable
- Current drug or alcohol use or dependence that interferes with study adherence
- Inability or unwillingness of participant or legal representative to give written informed consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
K
Karla Crockett
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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