Clinical trial Recruiting at 20 sites Observational Ages 18 to 75

Long-term follow-up of the Minder implanted EEG system for epilepsy care

Official title: A Prospective Long-Term Follow-Up Study to Evaluate the Use of the Minder Device to Aid in Treatment After Actionable Event Identification in Patients Diagnosed With Epilepsy.

Run by Epiminder America, Inc. · NCT07110454 · Data updated 2026-11-12

This follow-up will see if long-term use of the implanted Minder sub‑scalp EEG system helps doctors manage care for people with epilepsy whose seizures are not well captured by standard EEGs.

More Epilepsy trials

Quick facts

Study typeObservational
Ages18 Years to 75 Years
SexAll
Enrollment210 (estimated)
SponsorEpiminder America, Inc.
Industry-sponsored
Locations21 sites (Birmingham, Alabama and 20 other locations)
StatusRecruiting
StartedDecember 23, 2025
Main results expectedJanuary 2029
Study endsJanuary 2029
Registry record updatedOctober 22, 2026
Trial IDNCT07110454 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are people who enrolled in the DETECT program, received the implanted Minder device, completed DETECT by having an actionable event or the 6‑month visit, and still have the device implanted.

Probably not a fit

Patients who never received the Minder implant, who require MRI or other contraindicated procedures, or whose seizures are already well captured and controlled with standard monitoring are unlikely to benefit from this follow‑up.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational long‑term follow‑up of participants who previously received the implanted Minder sub‑scalp EEG device in the DETECT program. The study collects periodic information on general wellbeing, healthcare use, and participants' experience using Minder data after an actionable event or completion of the 6‑month DETECT visit. Participants remain under the care of their treating physicians while study staff document how Minder data are used in routine clinical decision‑making. The Minder System has FDA De Novo classification and is being followed in real‑world settings at participating centers.

Why it matters

Potential benefit: If successful, long‑term Minder monitoring could help clinicians detect events missed by standard EEG and guide treatment changes that reduce seizures and improve quality of life.

How similar studies have gone: Prior data from the DETECT program supported FDA De Novo clearance of the Minder system, but long‑term outpatient outcomes and real‑world use patterns are less well characterized.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Participant met all inclusion criteria, was enrolled in the DETECT study, and received the Minder device
* Participant completed the DETECT study by receiving an actionable event or by completing the 6-month follow-up visit
* Participant continues to have the Minder device implanted
* Participant must continue to meet relevant DETECT study inclusion criteria

Exclusion Criteria:

* Participant meets any relevant DETECT study exclusion criteria including needing treatments or assessments that are not indicated with the Minder System like Magnetic Resonance Imaging (MRI)

Where it's running

  • UAB Epilepsy Center
    Birmingham, Alabama, United States
    Recruiting
  • Mayo Clinic - Arizona
    Phoenix, Arizona, United States
    Recruiting
  • Stanford
    Palo Alto, California, United States
    Recruiting
  • Stanford
    Palo Alto, California, United States
    Recruiting
  • UC San Diego Health
    San Diego, California, United States
    Recruiting
  • Yale School of Medicine
    New Haven, Connecticut, United States
    Recruiting
Show 15 more locations
  • Mayo Clinic - Florida
    Jacksonville, Florida, United States
    Recruiting
  • Nicklaus Children's Hospital
    Miami, Florida, United States
    Recruiting
  • USF Health
    Tampa, Florida, United States
    Recruiting
  • Massachusetts General Hospital
    Boston, Massachusetts, United States
    Recruiting
  • Beth Israel Deaconess Medical Center
    Boston, Massachusetts, United States
    Recruiting
  • Michigan Medicine
    Ann Arbor, Michigan, United States
    Recruiting
  • University of Minnesota
    Minneapolis, Minnesota, United States
    Recruiting
  • Mayo Clinic - Rochester
    Rochester, Minnesota, United States
    Recruiting
  • Washington University
    St Louis, Missouri, United States
    Recruiting
  • Billings Clinic
    Billings, Montana, United States
    Recruiting
  • Atrium Health Neurosciences Institute - Charlotte
    Charlotte, North Carolina, United States
    Recruiting
  • Duke University
    Durham, North Carolina, United States
    Recruiting
  • University Hospitals Cleveland Medical Center
    Cleveland, Ohio, United States
    Recruiting
  • University of Pennsylvania
    Philadelphia, Pennsylvania, United States
    Recruiting
  • IU Health Neuroscience Center
    Indianapolis, Indiana, United States
    Enrolling by invitation

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.