跳至主要内容
临床试验/NCT02180958
NCT02180958已完成不适用

Evaluation of ONYX in ENDOVASCULAR Treatment of Cerebral AVMs. Prospective, Multi-center and Observational French Study

Medtronic Neurovascular Clinical Affairs17 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2014年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
140
试验地点
17
主要终点
Incidence of Device or procedure Adverse Events

研究概览

简要总结

To assess safety and efficacy of ONYX treatment for cAVM:

详细描述

The main objective of this study is to assess the safety at 1 month after any embolization session and the efficacy at:

  • 12 months post last embolization in case of treatment with embolization only
  • 12 months after additional treatment with neurosurgery
  • 36 months after additional treatment with radiosurgery

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
6 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The patient presents a cerebral AVM (not already treated) that can be treated by embolization with Onyx whether or not associated with a cyanoacrylate based adhesive,
  • The patient is at least 6 years old.

排除标准

  • During the treatment period for his/her cerebral AVM, the patient participates in a study assessing another medical device, another procedure or a drug.
  • The patient and/or his/her legal representative (if applicable) refuses to give his/her consent to the collection and processing of data required by the centralized follow-up. For patients who refused collection of their personal data, only, the reason for non inclusion and date of implantation will be documented.
  • Any condition that could prevent follow-up of the patient.

结局指标

主要结局

Incidence of Device or procedure Adverse Events

时间窗: 1 month

Device or procedure related adverse events

Healing rate

时间窗: 12 or 36 months

No residual early venous return * 12 months after last embolization in case of complete treatment or stopping treatment; * 12 months after additional intervention in case of additional treatment required by neuro-surgery; * 36 months after additional intervention in case of additional treatment required by radio-surgery.

次要结局

  • Describe funtional independence(1 and 12 months)

研究者

发起方
Medtronic Neurovascular Clinical Affairs
申办方类型
Industry
责任方
Sponsor

研究点 (17)

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