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临床试验/NCT03831672
NCT03831672Unknown不适用

Post Market Multi-Center Retrospective Research on Embolization of Intracranial Aneurysms With Pipeline Embolization Device in China (PLUS)

Beijing Neurosurgical Institute1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年11月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
200
试验地点
1
主要终点
Rate of complete aneurysm occlusion in 12 months

研究概览

简要总结

Pipeline TM embolization device launched to China in 2014, and has been widely used to treat large width IA. Therefore, it is necessary to collect and analysis the clinical data to evaluate effectiveness and safety of its usage in Chinese population, and this may guide the clinical practice and meet the clinical needs better.

详细描述

Recent years, the rapid development of endovascular treatment, especially the introduction of blood flow diverter device, has led to a new step in the treatment of intracranial aneurysms. It is different from usual treatment concept, blood flow diverter device's innovation is guiding to its parent artery reconstruction by cutting into the blood flow velocity and flow rate to the IA, and, promote the forming of aneurysm cavity thrombosis and the Neointima growth of IA's neck, so that to achieve aneurysm treatment.

A number of multi-center clinical studies on Pipeline embolization devices (PED, Ev3 Company/Medtronic, USA) have been conducted in North America and Europe recently. Becske etc reported the result of one multi-center prospective clinical trial of North America (PUFS), the PED treats the complicated intracranial internal carotid artery aneurysm. At the time of 180 days, 1 year, 3 years follow-up, the complete occlusion rate were 73.6%, 86.8% and 93.4% respectively. O 'kelly etc. the study showed that the rate of subtotal occlusion over 1 year follow-up of PED treatment for complex intracranial aneurysms was 90%. Many studies have confirmed the effectiveness of PED in the treatment of complex intracranial aneurysms.

The main motivation to innovate the blood flow diverter device is to use it to treat some large or giant aneurysms, fusiform aneurysm which can't be treated well by ordinary interventional embolization methods. So, in the initial stage of the application, its indications are mainly focus on the large or giant aneurysms located in the internal carotid artery before the origin of the posterior communicating artery. In recent years, the blood flow diverter devices were already used to treat many kinds of IA in almost all parts of the brain, different sizes and with pathological changes, such as dissecting aneurysms and vesicular aneurysms.

Although there was already much clinical research evidence which proved the efficacy and safety of PipelineTM 's treatment to the aneurysm as the embolization device, but these data are all from the foreign population, there is still no published clinical evidence of large sample size clinical study of Chinese population. Pipeline has been widely used to treat large width IA. Therefore, it's meaningful to evaluate effectiveness and safety in Chinese population, and this may guide the clinical practice and meet the clinical needs better.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients accepting to participate the study
  • Patients treated with Pipeline

排除标准

  • Patients treated by parent vessel occlusion
  • Patients treated by other stent
  • Patients lacking 3-dimensional aneurysm images or the images not satisfied the simulation

结局指标

主要结局

Rate of complete aneurysm occlusion in 12 months

时间窗: assessed at 12 months (plus or minus 3 months) after procedure

Complete occlusion defined as no contrast in contact with the IA neck or with the wall of the IA sac

Occurrence of ipsilateral major stroke or neurovascular death in 12 months

时间窗: assessed at 12 months (plus or minus 3 months) after procedure

Including but not limited: Spontaneous rupture of the target aneurysm, Ipsilateral intracranial hemorrhage, Ischemic stroke, Symptomatic parent artery stenosis, Permanent cranial neuropathy

次要结局

  • Rate of Complete aneurysm occlusion in 24 months(assessed at 24 months (plus or minus 6 months) after procedure)
  • Device-related neurologic adverse event in 12 months(assessed at 12 months (plus or minus 3 months) after procedure)
  • Occurrence of ipsilateral major stroke or neurovascular death in 24 months(assessed at 24 months (plus or minus 6 months) after procedure)
  • Rate of Complete aneurysm occlusion in 6 months(assessed at 6 months (plus or minus 3 months) after procedure)
  • Occurrence of ipsilateral major stroke or neurovascular death in 1 month(assessed at 1 month (plus or minus 0.5 month) after procedure)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xinjian Yang, MD

Vice Chair of Department of Interventional Neuroradiology

Beijing Neurosurgical Institute

研究点 (1)

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