Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Epitel, Inc.
This is a prospective study to quantify Epitel's™ Remote EEG Monitoring System's (REMI™) ability to record electroencephalography (EEG) of seizure events in an ambulatory setting for extended periods (14 - 28 days). Patients presenting with questionable seizure characterization that are scheduling a conventional at home ambulatory EEG (Amb EEG) and who meet the study inclusion and exclusion criteria will be prescribed a REMI system.
The purpose of this study is to demonstrate that the REMI system is able to record EEG data that clinicians can use to identify ictal events over extended periods, and that extended clinical EEG data is valuable in the diagnosis and treatment of seizure related symptoms.
Age
18–70
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients have a reported history of seizures (epileptic, non-epileptic, or unknown),
Have a minimum reported seizure rate of one every two weeks,
Are prescribed an ambulatory EEG study as part of routine care,
Is Male or Female between the ages of 18 and 70,
Can understand and sign written informed consent, or have a legal guardian provide consent,
The Patient (or Primary Caregiver) must be competent to follow all study procedures,
The Patient must be willing to use the System for a prolonged period (up to 30 days), for a minimum of 20 hours/day.
You may not be if
Is sensitive or allergic to medical acrylics, silicones, or hydrogels,
Is enrolled in another investigational drug or device trial,
Is homeless or in a home without a power supply, or
Cannot read, speak, or understand English (and does not have a translator).
Clareo Health | Impact of Capturing Ictal Events With Ultra-long-term Ambulatory EEG Monitoring With Remote EEG Monitoring System.
