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临床试验/NCT03504436
NCT03504436已完成不适用

Evaluation of the LEO + Stent in the Endovascular Treatment of Wide Neck Intracranial Aneurysms (Fusiform, Saccular or Dissecting), Ruptured or Not Ruptured: Cohort of the Self-expanding Intracranial Stent LEO

Balt Extrusion0 个研究点目标入组 176 人开始时间: 2015年3月15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
176
主要终点
Total aneurysmal occlusion rate

研究概览

简要总结

This is a prospective, multicenter, single-arm observational study to evaluate the efficacy and the morbi-mortality of LEO + in patients with wide neck intracranial aneurysms (fusiform, saccular or dissecting), ruptured or not ruptured.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • All patients with ruptured or not ruptured intracranial aneurysms demonstrated by cerebral arteriography treated with LEO + stent
  • Patients (or their parents for minors) must be informed and give written consent

排除标准

  • Patients (or parents) who refused to give consent.

结局指标

主要结局

Total aneurysmal occlusion rate

时间窗: 18 months

Classification of the occlusion observed angiographically as "complete occlusion", "residual neck" or "residual aneurysm" using the Montreal three-grade scale

Morbi-mortality

时间窗: 18 months

Number of complications and/or device or procedure related adverse events

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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