跳至主要内容
临床试验/NCT04572230
NCT04572230进行中(未招募)不适用

IMPACT: International Post Market Product Surveillance Study of IntrACranial Aneurysms Treated With an Endovascular Approach

Stryker Neurovascular32 个研究点 分布在 7 个国家目标入组 405 人开始时间: 2020年12月21日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
405
试验地点
32
主要终点
Primary Performance Measure

研究概览

简要总结

IMPACT is an observational, post market study designed to provide an ongoing safety and performance evaluation of Stryker Neurovascular devices used for the treatment of intracranial aneurysms with an endovascular approach.

详细描述

IMPACT is an international, prospective, observational, multicenter, non-randomized, post market study designed to provide ongoing safety and performance evaluation on implantable devices used for the treatment of intracranial aneurysms with an endovascular approach. Data collection will also include details on adjunctive and ancillary devices used.

In addition, to gaining safety and performance data, this study will provide clinical evidence that may assist physicians in selecting an appropriate device(s) while describing treatment options used to treat patients with intracranial aneurysms.

研究设计

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

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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Primary Performance Measure

时间窗: 12 months

Composite of 100% occlusion of the target aneurysm without significant parent artery stenosis per independent core lab assessment and with no target aneurysm retreatment

Primary Safety Endpoint

时间窗: 12 months

Stroke-related neurological death or Disabling stroke in the target vessel territory as adjudicated by an independent Clinical Events Committee (CEC)

次要结局

  • Secondary Performance Measures(Through 24 months)
  • Secondary Safety Endpoints(Through 24 months)

研究者

发起方
Stryker Neurovascular
申办方类型
Industry
责任方
Sponsor

研究点 (32)

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