跳至主要内容
临床试验/NCT07166926
NCT07166926招募中不适用

Mobile Pediatric Thoracic and Abdominopelvic Computed Tomography (CT)

Duke University1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2025年11月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
25
试验地点
1
主要终点
Number of Images With Good or Acceptable Quality

研究概览

简要总结

A special kind of CT scanner that can move around (called a mobile CT) is already approved by the FDA to take pictures of adult and pediatric heads. This study wants to see if the same machine can safely take pictures of the chest and belly (abdomen) in children. This may benefit pediatric patients who may need a CT but are otherwise unable to be safely transported to the radiology department.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
— 至 5 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Patient <5 years of age or meeting size criteria to fit into the CT gantry and field of view (35 cm gantry aperture, 26 cm field of view).
  • •Patients who would benefit from cross-sectional imaging (CT) of the chest and/or abdomen and pelvis, based on severity and anticipated progression of their disease, as determined by their primary treatment team or recommended by a consultant team.
  • •Patients who are deemed clinically unsafe to travel based on medical conditions as determined by their primary treatment team.

排除标准

  • •Size precludes safe operation of the CT gantry
  • •Unable to consent and parent/guardian unable to consent.

研究组 & 干预措施

Mobile CT for pediatric patients in NICU, CVICU, and PICU

Other

Pediatric patients in NICU, CVICU, and PICU who are too ill to transport to the radiology department; could benefit from imaging for diagnosis and care. Advanced imaging modalities like CT can provide critical insights for monitoring pediatric patients with certain conditions.

干预措施: Mobile CT (Device)

结局指标

主要结局

Number of Images With Good or Acceptable Quality

时间窗: From enrollment to interpretation of the scan (up to approximately 48 hours)

Image quality will be considered good/acceptable if there is a clinical report. Otherwise it is unacceptable.

次要结局

未报告次要终点

研究者

发起方
Duke University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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