ACTRN12622000112763已完成未知
Clinical safety study to assess the safety, feasibility and acceptability of a long-term, continuous monitoring, wearable electroencephalography (EEG) device in ischemic stroke patients
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 17
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Diagnosis
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Male and female patients with CT or MRI confirmed ischemic stroke.
- •18 years and older.
- •Patients have received appropriate stroke treatment and are now in the stroke ward for monitoring (for at least 9 hours) before being discharged
排除标准
- •Haemorrhagic stroke, stroke mimic, transient ischemic attack, or no stroke.
- •Brain surgery or any intervention or condition that will prevent patient from wearing
- •a head device for 9 hours.
- •Patient is already being monitored using EEG equipment.
- •Patient has a history of epilepsy and/or seizures.
- •Younger than 18 years old.
- •Patient has brain or scalp implant.
- •Patient has a cognitive impairment that will make them more susceptible to forms
- •of discomfort or distress induced by wearing the device.
- •Patient is unable to complete the questionnaire with the help of a family member,
- •guardian, caregiver, or nurse.
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