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Recruiting No phase listed Observational

Diagnosing Epilepsy To EffeCT Change Long-Term Follow-Up

ClinicalTrials.gov ID: NCT07110454

Public ClinicalTrials.gov record NCT07110454. 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 Sep 3, 2026, 8:52 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

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.

Brief summary

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

The purpose of this research is to address the challenges of correctly monitoring, managing, and diagnosing epilepsy in participants whose seizures are not well captured by standard electroencephalography (EEG) tests and who cannot use or are not able to use more standard monitoring techniques. This research is being done to understand how the Minder System helps physicians make decisions about participant's epilepsy treatment after an actionable event. The Minder System was granted De Novo classification by the U.S. Food and Drug Administration (FDA) and is not investigational. Participants that have completed the DETECT study and received the Minder System previously will consent to join this long-term follow-up observational study. The study will collect information about general wellbeing, use of healthcare services, and experience using the Minder data over time to support long-term epilepsy care. All participants will continue to be followed by their treating physician and undergo assessments and visits every six (6) months until two (2) years after receiving the Minder device.

Study identification

NCT ID
NCT07110454
Recruitment status
Recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
Epiminder America, Inc.
Industry
Enrollment
210 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 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
May 31, 2026
Primary completion
Dec 31, 2028
Completion
Dec 31, 2028
Last update posted
Jul 14, 2026

2026 – 2029

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Mayo Clinic - Arizona Phoenix Arizona 85054 Recruiting
Stanford Palo Alto California 94304 Recruiting
Yale School of Medicine New Haven Connecticut 06510 Recruiting
Mayo Clinic - Florida Jacksonville Florida 32224 Recruiting
Nicklaus Children's Hospital Miami Florida 33155 Recruiting
USF Health Tampa Florida 33606 Recruiting
IU Health Neuroscience Center Indianapolis Indiana 46202 Enrolling by invitation
Massachusetts General Hospital Boston Massachusetts 02114 Recruiting
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 Recruiting
Mayo Clinic - Rochester Rochester Minnesota 55905 Recruiting
Washington University St Louis Missouri 63130 Recruiting
Atrium Health Neurosciences Institute - Charlotte Charlotte North Carolina 28204 Recruiting
Duke University Durham North Carolina 27710 Recruiting
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 Recruiting
University of Pennsylvania Philadelphia Pennsylvania 19104 Recruiting

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 NCT07110454, 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 Jul 14, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07110454 live on ClinicalTrials.gov.

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