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Epi-collect: Data Collection During Video EEG Monitoring and at Patient's Home

Epi-collect: Data Collection During Video EEG Monitoring and at Patient's Home

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03038191
Enrollment
28
Registered
2017-01-31
Start date
2017-03-08
Completion date
2019-06-30
Last updated
2021-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy

Brief summary

Epilepsy is a group of neurological disorders characterized by propensity for spontaneous epileptic seizures. Epileptic seizures are the result of excessive and abnormal nerve cell activity in the brain. About 0.7-1% of the world population suffers from seizures. The most common treatment is based on seizure medications that enables about 2/3 of the patients to control their seizures. However, about 20 million patients worldwide, suffer from unpredictable seizures without remedy, and are resistant to medication. In this study EEG and other physiologic signals are collected using wearable sensors, from Epilepsy patients who are at risk of experiencing seizures. The collected signals will be used for developing algorithms that may identify pre-seizure and seizure related periods.

Interventions

DEVICENeuroelectrics Enobio 8(R)

Monitoring

Sponsors

Medial Research Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age \>18 * Known diagnosis of Epilepsy * Expected to experience seizures during the period of the study as determined by the PI. * Able to meet with the Sponsor representative at home

Exclusion criteria

* Trauma/broken skin on forehead. * Patient can not follow or comply with instructions * Patients who are unable to independently provide an informed consent * Patients with major psychiatric co-morbidities * Patients with psychogenic non-epileptic seizures

Design outcomes

Primary

MeasureTime frameDescription
Successful data collection during hospitalization12 hours daily for up to 5 daysContinuous recording from wearable sensors of physiologic signals during hospitalization in the video EEG unit
Successful data collection during at home monitoring12 hours daily for up to 14 daysContinuous recording from wearable sensors of physiologic signals during at home monitoring

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026