跳至主要内容
临床试验/NCT03713450
NCT03713450终止不适用

A Prospective Single Centre Randomized Interventional Controlled Trial Comparing Patient and Staff Safety During Aorto-iliac Revascularization Procedures Under Automated Fusion Imaging Guidance With Controls

Nantes University Hospital2 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2019年1月10日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
45
试验地点
2
主要终点
Dose area product

研究概览

简要总结

Endovascular revascularization has revolutionized the field of vascular surgery and has become the first-choice treatment for peripheral arteries occlusive disease. However, the drawback of this technic is the X-ray exposure for both patients and staff and the iodinated contrast injection for the patient.

One way to reduce both radiation and contrast use is to use advanced imaging techniques allowing an overlay of a 3D vascular mask (from a pre-operative CT scan) onto the live X-ray image. This has been proven during endovascular aneurysm repair.

This advanced imaging application is currently available only in the latest expensive hybrid operating rooms, requires additional manoeuvre from the operator throughout the procedure, and may be X-rays and contrast consuming.

This trial will examine the clinical benefits based on patient and staff' radiation exposure during aorto-iliac revascularisation, of a new software imaging guidance, suitable for any theatre including those equipped with mobile C-arm, fully automated and with a radiation free overlay registration process.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

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

  • Male or female aged 18 or older,
  • Patients scheduled for aorto iliac endovascular revascularisation,
  • Pre-operative CT scan.

排除标准

  • Women of childbearing age,
  • Absence of preoperative CT scan,
  • Emergency procedures.

结局指标

主要结局

Dose area product

时间窗: The end of the procedure

Dose area product (DAP) by the end of the procedure.

次要结局

  • Number of DSA runs(The end of the procedure)
  • Operator exposure(The end of the procedure)
  • Contrast volume(The end of the procedure)
  • Operative time(The end of the procedure)
  • Air Kerma(The end of the procedure)
  • Fluoroscopy time(The end of the procedure)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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