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临床试验/NCT03984279
NCT03984279已完成不适用

Comparison of the Study Was to Compare Sequential Fluoroscopy Guidance With Spiral Guidance in Terms of Safety (Number of Major Complications), Effectiveness (Number of Targets Reached), Speed (Procedural Time) and Radiation (DLP) in Interventional Chest-abdomen-pelvic Procedures.

Centre Hospitalier Universitaire de Besancon1 个研究点 分布在 1 个国家目标入组 385 人开始时间: 2018年1月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
385
试验地点
1
主要终点
number of major complications

研究概览

简要总结

The purpose of the study was to compare sequential fluoroscopy guidance with spiral guidance in terms of safety (number of major complications), effectiveness (number of targets reached), speed (procedural time) and radiation (DLP) in interventional chest-abdomen-pelvic procedures.

研究设计

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

入排标准

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

入选标准

  • adult patients (> 18 years),
  • indication of interventional percutaneous diagnostic or therapeutic chest-abdomen-pelvic procedure under CT control

排除标准

  • MRI contra indication
  • persons referred to in Articles L1121-5 to L1121-8 of the French Public Health Code

结局指标

主要结局

number of major complications

时间窗: All patients with indication of interventional percutaneous diagnostic or therapeutic chest-abdomen-pelvic procedure under CT control performed on a period of 1 year will be taken into account

Comparison between the 2 groups

number of targets reached

时间窗: All patients with indication of interventional percutaneous diagnostic or therapeutic chest-abdomen-pelvic procedure under CT control performed on a period of 1 year will be taken into account

Comparison between the 2 groups

Dose Length Product (DLP)

时间窗: All patients with indication of interventional percutaneous diagnostic or therapeutic chest-abdomen-pelvic procedure under CT control performed on a period of 1 year will be taken into account

Comparison between the 2 groups

次要结局

  • number of controls required to place the needle(All patients with indication of interventional percutaneous diagnostic or therapeutic chest-abdomen-pelvic procedure under CT control performed on a period of 1 year will be taken into account)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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