ACTRN12619001684112尚未招募未知
An Early Feasibility Study to Obtain Imaging Data from Participants witha Diagnosed Stroke to Refine the Algorithm for the EMVision Brain Scanner
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 30
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
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1.Adults >=18 years of age.
- •2.Admitted to hospital with new neurological signs and confirmed diagnosis of stroke supported by conventional brain imaging.
- •3.Ability to provide informed consent. Participants will provide written informed consent. Where this is not possible, surrogate consent will be obtained.
- •4.Ability to adhere to study visit schedule and other protocol requirements.
- •5.Confirmed diagnosis of stroke within 72 hours of admission.
- •6.Head size deemed suitable for scanning with the EMVision brain scanner.
排除标准
- •1.Experiences seizures from onset of stroke, or known history of seizure episodes.
- •2.Has injury or known medical condition on the head that would not allow the placement of EMVision brain scanner.
- •3.Is unable to lie still for the duration of the scan.
- •4.Is not a suitable candidate according to the assessing investigator.
- •5.Has any metal implants in the head or neck for example stents, aneurism clips, surgical clips, pressure monitors and drains.
- •6.Is known to be pregnant or lactating.
研究者
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