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临床试验/NCT03988062
NCT03988062已完成不适用

Aneurysm Packing With the Expandable TrelliX Coil System - A Prospective Safety Study

Shape Memory Medical, Inc.2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2018年11月21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
13
试验地点
2
主要终点
Safety - Serious adverse events

研究概览

简要总结

APEX-FIH is a first-in-human, open-label prospective multicenter study of the TrelliX Embolic Coil System for use in embolization of the medium to large, ruptured or unruptured cerebral aneurysms

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subject age ≥18 and ≤80 years with a diagnosis of a ruptured or unruptured intracranial aneurysm judged suitable for selective endovascular treatment by coil occlusion during single procedure
  • Aneurysm size [largest measurement from the cross sectional images to determine overall aneurysm size, not just the lumen) ≥5 mm and ≤16mm
  • If ruptured aneurysm: either WFNS grade 1 or 2, or Hunt and Hess 1 or 2
  • If unruptured aneurysm: Subject grade Modified Rankin Scale mRS 0 - 2
  • Investigator plans to use ≥70% in volume TrelliX coils to fill target aneurysm

排除标准

  • Prior treatment (surgical or endovascular) of the target aneurysm
  • Planned treatment of multiple aneurysms in index procedure
  • Planned use of other modified coils (Matrix, HydroCoil or fibered coils)
  • Planned use of liquid embolic material
  • Life expectancy less than 12 months
  • Presence of arteriovenous malformation
  • Fusiform, mycotic, traumatic, or tumoral aneurysms
  • Intended or planned aneurysm treatment by parent vessel occlusion
  • Clipping or endovascular treatment of another intracranial aneurysm performed within 30 days before or planned within 30 days following the index procedure

结局指标

主要结局

Safety - Serious adverse events

时间窗: 30 days

Rate of freedom from incidence of serious adverse events related to the study

Efficacy - Angiographic occlusion

时间窗: 6 months and 12 months

Rate of angiographic occlusion based on Raymond-Ray grading scale \[1 No filling of aneurysm neck or dome; 2 Residual filling of aneurysm neck, not dome; 3 Residual filling of aneurysm neck and dome (worst outcome)\]

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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