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NCT07110454 · ClinicalTrials.gov registry record

Diagnosing Epilepsy To EffeCT Change Long-Term Follow-Up

A clinical trial of Epilepsy and Epilepsy (Treatment Refractory), sponsored by Epiminder America.

Recruiting
Registry status
210
Enrollment target
7
Study locations

NCT07110454 is a study of Epilepsy and Epilepsy (Treatment Refractory) that is actively recruiting participants, run by Epiminder America. The registered enrollment target is 210 participants, below the 951-participant average among 160 other Epilepsy trials with a reported enrollment target (78% lower). The trial reports 7 study locations across 7 states.

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The verdict

NCT07110454, a study of Epilepsy and Epilepsy (Treatment Refractory), is actively recruiting participants, sponsored by Epiminder America.

RECRUITING
Registry status
210 participants
Enrollment target
7
Study locations

Study Summary

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.

Interventions

  • DEVICE Previous receipt of the Minder System (implantable continuous electroencephalographic (EEG) monitoring (iCEM) system)

Study Locations (7)

Arizona

  • Mayo Clinic - Arizona - Phoenix

Connecticut

  • Yale School of Medicine - New Haven

Florida

  • Mayo Clinic - Florida - Jacksonville

Massachusetts

  • Beth Israel Deaconess Medical Center - Boston

Minnesota

  • Mayo Clinic - Rochester - Rochester

Missouri

  • Washington University - St Louis

Pennsylvania

  • University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 210 participants
Start Date 2026-06
Est. Completion 2029-01

Sponsor

Epiminder America

2 total trials

What the Registry Record Tells You About NCT07110454

The ClinicalTrials.gov registry entry for NCT07110454 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 210 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 951-participant average among 160 other Epilepsy trials with a reported enrollment target (78% lower). The listed sponsor is Epiminder America, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Epilepsy appearing as the primary indexed condition, and to 1 intervention - of which Previous receipt of the Minder System (implantable continuous electroencephalographic (EEG) monitoring (iCEM) system) is the first listed.

NCT07110454 reports 7 study locations spanning 7 distinct geographic areas - top geographies include Arizona, Connecticut, Florida.

Frequently Asked Questions

What is clinical trial NCT07110454 about?

NCT07110454 is a clinical study titled "Diagnosing Epilepsy To EffeCT Change Long-Term Follow-Up". 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...

What is the current status of trial NCT07110454?

This trial is currently recruiting. The enrollment target is 210 participants. The study started on 2026-06. Estimated completion is 2029-01.

What conditions does trial NCT07110454 study?

This clinical trial studies the following conditions: Epilepsy, Epilepsy (Treatment Refractory).

What interventions are being tested in trial NCT07110454?

The interventions under investigation include: Previous receipt of the Minder System (implantable continuous electroencephalographic (EEG) monitoring (iCEM) system) (DEVICE).

Who is sponsoring clinical trial NCT07110454?

This trial is sponsored by Epiminder America, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07110454 being conducted?

This trial has 7 study locations across Arizona, Connecticut, Florida, Massachusetts, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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