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Using brain wave recordings to tell apart two types of stroke

Studies brain wave recordings in adults with acute ischemic or hemorrhagic stroke.

Plain-language title generated from the registry record
Registry title: Role of EEG in Differentiation Between Ischemic and Hemorrhagic Stroke

Key facts

Where
Asyut, EgyptSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT06984965, who can take part

Where in Egypt

  • Neurology Department, Faculty of Medicine, Assiut UniversityAsyut, EgyptTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Assiut University
Trial code
NCT06984965
Record updated
5 November 2026
Original description
Searching electrical activity registered by EEG in acute ischemic and hemorrhagic stroke and comparing these parameters to the post-stroke recovery patterns to investigate the role of EEG as a differentiation tool and as a predictor of post-stroke recovery.Read full original descriptionShow less

Electroencephalogram (EEG) in Differentiation Between Ischemic and Hemorrhagic Stroke and Its Role as a Predictor of Post-stroke Recovery

Searching electrical activity registered by EEG in acute ischemic and hemorrhagic stroke and comparing these parameters to the post-stroke recovery patterns to investigate the role of EEG as a differentiation tool and as a predictor of post-stroke recovery.

Inclusion: Age above 18 and below 80 years; Acute Ischemic stroke: ischemic arteria cerebri media infarct confirmed by MRI; Acute Hemorrhagic stroke: spontaneous intraparenchymal bleeding confirmed by CT; Stroke onset <72 hours before expected time of performing EEG; First-ever ischemic stroke; Measurable deficit on the National Institute of Health Stroke Scale (NIHSS); Able to give and sign informed consent.

Exclusion: Previous neurological procedure (metallic implant, brain pace, cranial operation history); Alcohol or drug addiction; Patients with subarachnoid haemorrhage, traumatic haemorrhage (epidural/subdural bleeding), cerebral venous sinus thrombosis, indication for urgent neurosurgical intervention; History of other central nervous system diseases; Injury or active infection of electrode cap placement area; Claustrophobia; recognition disorder; Significant physical impairment that would restrict the ability to use the portable EEG devices; Presence of malignancy or systemic rheumatic disease; Non-stroke disease or lesion affecting the sensorimotor system; Presence of Malignancy; Presence of severe cognitive impairment; History of epilepsy or taking medication due to epilepsy; Transient Ischemic Attacks (TIAs); Greater than 72 hours past the initial insult; Any signs unfit for MRI/EEG scan; Known skull defect or head trauma; Presence of pump/shunt.

ClinicalTrials.gov NCT06984965