Altered Mental Status Clinical Trial
Official title:
Diagnostic Utility of Emergency Electroencephalography in Identifying Non-convulsive Seizure and Subclinical Status Epilepticus in Patients With Altered Mental Status
Verified date | February 2012 |
Source | Bio-Signal Group Corp. |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
The aim of the proposed research is to compare the diagnostic accuracy of a portable
wireless electroencephalography (EEG) device (Biosignal Micro-EEG) to standard EEG in
identifying abnormal EEG patterns (mainly non-convulsive seizure and non-convulsive status
epilepticus) in emergency department (ED) patients with altered mental status. Comparing the
the accuracy of EEG recordings and interpretations of Micro-EEG to those of standard EEG
will allow the investigators to assess the utility of this novel device in the ED patients
with altered mental status. The unique qualities of Micro-EEG device could potentially
facilitate easier access to EEG test in all ED patients.
This study will also provide valid information regarding the prevalence of non-convulsive
seizure in ED patients with altered mental status.The gold standard for diagnosing
non-convulsive seizure would be standard EEG.
All study participants will undergo electroencephalography using the two devices (standard
EEG and micro-EEG) and a combination of standard electrodes and Electro-Cap in a randomized
order: 1. Standard EEG with standard EEG electrodes, 2. Micro-EEG with standard EEG
electrodes, and 3. Micro-EEG with Electro-Cap electrodes.
Status | Completed |
Enrollment | 261 |
Est. completion date | February 2012 |
Est. primary completion date | February 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 13 Years and older |
Eligibility |
Inclusion Criteria: ED patients = 13 year-old with AMS on arrival to ED Exclusion Criteria: 1. Patients with apparent and immediately correctable cause of AMS upon presentation (determined by ED attending physician during initial evaluation): - Patients with finger stick or serum glucose less than 60 mg/dl - Patients with hypothermia - Patients with hyperthermia, heat exhaustion or heat stroke - Patients with opioid overdose responding to Narcan 2. Patients who cannot undergo EEG recordings because of severe head and injury, hemodynamic instability, transfer to operating room, etc.) 3. Hemodynamically unstable patients (SBP < 90 mmHg) 4. Uncooperative or combative patients on whom the EEG simply cannot be obtained. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | 450 Clarkson Avenue | Brooklyn | New York |
Lead Sponsor | Collaborator |
---|---|
Bio-Signal Group Corp. | Kings County Hospital, National Institute of Neurological Disorders and Stroke (NINDS), State University of New York - Downstate Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Diagnostic Utility of Emergency Electroencephalography in Identifying Non-convulsive Seizure and Subclinical Status Epilepticus in Patients with Altered Mental Status (AMS) | Sensitivity, specificity, positive/negative likelihood ratios of micro-EEG in identifying non-convulsive seizures and abnormal brain activities The concordance of EEG interpretations between micro-EEG and standard EEG recordings |
6 months | No |
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