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Clinical Trial Summary

The purpose of this study is the validation of an Electroencephalograph based algorithm for detection of onset and deterioration of Acute Ischemic Stroke by Comparison to NIHSS.


Clinical Trial Description

Inclusion criteria study population

1. Age > 18 years old.

2. Acute stroke symptoms onset within 2 weeks of inclusion, and as proximate to event as possible and as long as there was no neurological deterioration (ΔNIHSS>4) from symptoms onset to inclusion.

3. Patients with TIA lasting at least 5 minutes or minor acute ischemic stroke (NIHSS < 4 at the time of enrolment)

4. More than 3 of the following:

Blood pressure >140/90 or unknown, Irregular heartbeat, Atrial Fibrillation, Smoker, Cholesterol >240 or unknown, Has Diabetes, Lack of physical exercise, Overweight, Has Stroke in the family

OR between 4 and 6 of the following:

Blood pressure 120-139/80-89, Unknown Irregular heartbeat, Atrial Fibrillation, Trying to quit smoking, Cholesterol 200-239, Borderline Diabetes, Some exercise, Slightly overweight, Not sure if Stroke occurred in family

Exclusion criteria study population

1. Intracranial hemorrhage on admission by CT.

2. Previous major hemispheric stroke.

3. Patients with pure sensory symptoms,

4. Significant movement disorder.

5. Local skull or skin affliction which prevents sensor application.

6. Any known condition which in the opinion of the investigator may interfere with the protocol implementation. ;


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01738412
Study type Observational
Source Neurokeeper Technologies
Contact Shay Bar Haim, Msc
Phone 972506822824
Email shaybarhaim@neurokeeper.com
Status Not yet recruiting
Phase N/A

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