EligibleTrials

Diagnosing Epilepsy To EffeCT Change Long-Term Follow-Up

Recruiting · NCT07110454 · Observational (researchers observe without assigning treatment) · Lead sponsor: Epiminder America, Inc.

View the official record on ClinicalTrials.gov →
Epilepsy

Interventions studied

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

What this trial is about

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.

Who can take part

Age range
18 Years to 75 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)

Inclusion criteria

Exclusion criteria

Where it is running

18 locations listed across 13 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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