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RECRUITING

Diagnosing Epilepsy To EffeCT Change Long-Term Follow-Up

NCT07110454 · View on ClinicalTrials.gov ↗

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

29 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07110454

The ClinicalTrials.gov registry entry for NCT07110454 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 210 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Epiminder America, which has 29 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07110454 reports 7 study locations spanning 7 distinct geographic areas — top geographies include Arizona, Connecticut, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

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). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07110454?

This trial is sponsored by Epiminder America, which has 29 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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