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临床试验/NCT06797765
NCT06797765已完成不适用

Optical Coherence Tomography Angiography in Neurological Disease: A Pilot Study

University of Texas Southwestern Medical Center2 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2024年10月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
7
试验地点
2
主要终点
Vascular and Perfusion Density in healthy controls

研究概览

简要总结

Optical Coherence Tomography Angiography (OCTA) is a non-invasive tool that images the neurovascular structures of the eye by using near-infrared light. Previous literature has demonstrated the potential of OCTA as a screening tool in stroke, but its utility in other neurological illness such as intracranial hemorrhage is unclear. Hence, this pilot study will gather preliminary data to support future grant applications to investigate this area more fully by recruiting patients with neurological illness and healthy controls and comparing their OCTA imaging parameters.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age 18 years or older
  • •Patient admitted to the neuroscience intensive care unit with a diagnosis of: subarachnoid hemorrhage, intracerebral hemorrhage, intracranial aneurysm (ruptured or unruptured), intracranial vascular malformation, ischemic stroke, seizure disorder, intracranial infection, intracranial tumor(s), inflammatory demyelinating disease, traumatic brain injury and/or neuromuscular respiratory failure OR subjects from the community without major neurologic, cardiovascular, pulmonary or metabolic disease

排除标准

  • •Pregnancy
  • •Non-English speaking
  • •GCS motor score less than 6 (i.e. must be able to follow commands)
  • •Temporary or permanent physical limitation that renders the patient unable to sit up and look inside OCTA device

研究组 & 干预措施

Control

Normal healthy human subjects

干预措施: OCTA (Device)

Patients

Patients with neurological disease

干预措施: OCTA (Device)

结局指标

主要结局

Vascular and Perfusion Density in healthy controls

时间窗: Once (approx. 10 mins)

Quantitative measure of retinal microperfusion. No definite time points are defined since different neurological diseases have different patterns of evolution and patient/provider availability may change.

Vascular and Perfusion Density in Patients with neurological disease

时间窗: Throughout study completion up to 28 days

Quantitative measure of retinal microperfusion. No definite time points are defined since different neurological diseases have different patterns of evolution and patient/provider availability may change.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Noah Jouett

Assistant Professor

University of Texas Southwestern Medical Center

研究点 (2)

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