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CompletedNCT03103425Updated Apr 6, 2017

Evaluation of StatNet Device for Electroencephalogram (EEG) Recordings

An observational study in Epilepsy and Seizures, sponsored by Beth Israel Deaconess Medical Center. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-04-06.

Sponsored by Beth Israel Deaconess Medical Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of the study is to develop an emergency electroencephalogram (EEG) device, StatNet, that can be placed quickly by minimally-trained personnel and interpreted remotely for rapid identification of seizures.

02

Conditions studied

  • Epilepsy
  • Seizures

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Keywords

  • New onset seizures
03

In context

Seizures

881 studies on the registry are indexed under Seizures; 144 are open to participants now.

This study's enrollment of 40 is below the median of 150 across 235 observational studies indexed under Seizures.

Browse Seizures studies →

Lead sponsor

Beth Israel Deaconess Medical Center is the lead sponsor of 560 studies on the registry; 80 are open to participants now.

Of its 75 completed or terminated interventional studies of FDA-regulated products, 61 (81%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Outpatients Inpatients

Inclusion criteria

  • Adults > age 18
  • Epileptiform discharges present on routine EEG

Exclusion criteria

Exclusion Criteria:

  • Open head wounds
  • Medically Unstable
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (actual)
06

Study locations

1 site
  • Beth Israel Deaconess Medical Center
    Boston, Massachusetts 02215, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 6, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT03103425
Lead sponsor
Beth Israel Deaconess Medical Center
Collaborators
HydroDot, Inc.
Responsible party
Trudy Pang (Instructor in Neurology, Beth Israel Deaconess Medical Center) — Principal investigator
First posted
Apr 6, 2017
Start date
Jun 2009
Primary completion
Jun 1, 2014
Completion
Jun 1, 2014
Last update
Apr 6, 2017

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2017. You cannot join it, but the record below documents what was studied.

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