Electroencephalograph for Detection of Acute Ischemic Stroke
Overview
The purpose of this study is Collecting data for an Electroencephalograph based algorithm for detection of onset and deterioration of Acute Ischemic Stroke by Comparison to NIHSS.
Full Title of Study: “Collecting Data for an Electroencephalograph Based Algorithm for Detection of Onset and Deterioration of Acute Ischemic Stroke by Comparison to NIHSS”
Study Type
- Study Type: Observational
- Study Design
- Time Perspective: Prospective
Detailed Description
Inclusion criteria study population Age > 18 years old. Acute stroke symptoms onset within 120 hours of inclusion, and as proximate to event as possible. Acute ischemic moderate or severe hemispheric stroke (assessed as 5 points or more by NIHSS) and including patients treated by t-PA Exclusion criteria study population Primary intracranial hemorrhage on admission by CT. Significant movement disorder. Previous major hemispheric stroke. Local skull or skin affliction which prevents electrodes application. Any known condition which in the opinion of the investigator may interfere with the protocol implementation. Inclusion criteria Control Population Age > 18 years old. Exclusion criteria Control Population Primary intracranial hemorrhage on admission by CT. Significant movement disorder. Previous major hemispheric stroke. Local skull or skin affliction which prevents electrodes application. Migraine Any known condition which in the opinion of the investigator may interfere with the protocol implementation.
Interventions
- Device: Neurokeeper stroke detector
- Monitoring stroke patients
Arms, Groups and Cohorts
- Study population
- Stroke patients
Clinical Trial Outcome Measures
Primary Measures
- Detection of stroke
Secondary Measures
- Correlation to severity of stroke
Participating in This Clinical Trial
Inclusion Criteria
- Age > 18 years old. – Acute stroke symptoms onset within 120 hours of inclusion, and as proximate to event as possible. – Acute ischemic moderate or severe hemispheric stroke (assessed as 5 points or more by NIHSS) and including patients treated by t-PA Exclusion Criteria:
- Primary intracranial hemorrhage on admission by CT. – Significant movement disorder. – Previous major hemispheric stroke. – Local skull or skin affliction which prevents electrodes application. – Any known condition which in the opinion of the investigator may interfere with the protocol implementation
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: N/A
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
Investigator Details
- Lead Sponsor
- Neurokeeper Technologies
- Provider of Information About this Clinical Study
- Sponsor
- Overall Contact(s)
- Shay Bar Haim, Msc, 972506822824, shaybarhaim@neurokeeper.com
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