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临床试验/NCT07760649
NCT07760649尚未招募不适用

A Post-market Observational Study to Monitor Safety and Effectiveness in the Treatment of Patients With Ischemic Stroke Using Commercially Approved J&J MedTech Devices Optimized for Neurovascular Thrombectomy

Neuravi Limited3 个研究点 分布在 2 个国家目标入组 5,000 人开始时间: 2026年8月10日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
5,000
试验地点
3
主要终点
Revascularization (Modified Thrombolysis in Cerebrovascular Infarction [mTICI])

研究概览

简要总结

The purpose of this study is to collect medical information to monitor the ongoing safety of the J&J MedTech devices and to understand how well they work when routinely used to treat participants with acute ischemic stroke (a condition caused by a blocked blood vessel in the brain).

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

  • Participant is 18 years of age or older at the time of consent
  • Informed Consent has been provided by the participant or the participants' legally authorized representative (LAR)
  • Participants with angiographic confirmation of acute ischemic stroke
  • A clinical decision has been made to treat the participant with an eligible Johnson & Johnson MedTech neuro-thrombectomy device independently and prior to enrollment in the study

排除标准

  • Known pregnancy, as evidenced by positive pregnancy test for women of childbearing potential or breast feeding
  • Current involvement in an investigational (drug, device, etcetera) clinical study that may confound study endpoints. Sponsor approval is required prior to enrollment

研究组 & 干预措施

Participants With Acute Ischemic Stroke

Participants with angiographic confirmation of acute ischemic stroke who are scheduled to undergo/have undergone mechanical thrombectomy using one or more of the study devices will be enrolled. Participants will have the procedure according to the standard of care (SOC) process of the hospital and physician preference. No treatment will be provided by the sponsor as a part of this study.

结局指标

主要结局

Revascularization (Modified Thrombolysis in Cerebrovascular Infarction [mTICI])

时间窗: Up to 90 days post-procedure

Revascularization is defined as achieving a specific minimum mTICI score, such as 2b or greater. mTICI is a 6-point grading system for determining the response of thrombolytic therapy for ischaemic stroke with grades as follows: mTICI 0 = no perfusion; mTICI 1 = penetration but not perfusion; mTICI 2a = some perfusion with distal branch filling of less than (\<)50 percent (%) of territory visualized; mTICI 2b = substantial perfusion with distal branch filling of \>=50% of territory visualized; mTICI 2c = near-complete perfusion; mTICI 3 = complete perfusion.

次要结局

  • Percentage of Participants With Modified Rankin Scale (mRS) Score of <=2 or no Worsening at 90 Days(At 90 days post-procedure)
  • 90-Day All-Cause Mortality(At 90 Days Post-Procedure)

研究者

发起方
Neuravi Limited
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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