跳至主要内容
临床试验/NCT04437862
NCT04437862已完成不适用

A Prospective, Multi-Center, Single Arm Study to Evaluate the Q Revascularization System for Neurointervention in Acute Ischemic Stroke: The EvaQ Study

MIVI Neuroscience, Inc.16 个研究点 分布在 2 个国家目标入组 121 人开始时间: 2020年10月27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
121
试验地点
16
主要终点
Symptomatic intracranial haemorrhage rate

研究概览

简要总结

Assess the safety and efficacy of the Q Revascularization System to remove thrombi and emboli from the neurovasculature in patients experiencing an acute ischemic stroke

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 years or older.
  • Pre-stroke independent functional status in activities of daily living with mRS 0-
  • A disabling stroke defined as NIHSS ≥ 6
  • In USA thrombolytic therapy (IV tPA) received within 3 hours of onset/ last known well, in Europe treatment with IV tPA received within 4.5 hours from onset/ last known well OR ineligibility for thrombolytic therapy
  • Endovascular treatment intended to be initiated < 8 hours from onset of symptoms or last known well time
  • Confirmed symptomatic large vessel occlusion of the intracranial internal carotid artery, middle cerebral artery, M1, M2, basilar or intracerebral vertebral artery by baseline neuroimaging CTA/MRA and angiographic imaging with a mTICI Score 0-1
  • For strokes in the anterior circulation the following imaging criteria should also be met: MRI criterion of volume of diffusion restriction visually assessed ≤50 mL OR CT criterion of ASPECTS 6 to 10 on baseline CT or CTA-source images or, significantly lowered cerebral blood volume (CBV) ≤50 mL
  • For strokes in the basilar or vertebral artery, the following imaging criterion should also be met: pc-ASPECTS score 8 to 10 on baseline CT, CTA-source images, or MRI
  • Signed informed consent from subject, acceptable person responsible (e.g. LAR) and/or according to County specific regulatory requirements and local ethical committee or review board requirements

排除标准

  • CT or MRI evidence of intracranial hemorrhage on presentation
  • CT or MRI showing mass effect or intracranial tumor (meningioma > 2 cm in diameter).
  • Previous stroke within the past 3 months
  • Rapidly improving neurological status as determined by Investigator/Neurologist
  • Renal failure/insufficiency with >3.0 mg/dL creatinine prior to procedure
  • Severe, sustained hypertension resistant to treatment (SBP >185 mmHg or DBP >110 mmHg)
  • Use of warfarin anticoagulation with International Normalized Ratio (INR) > 3.0 at the time of the procedure or any known hemorrhagic or coagulation deficiency
  • For patients who have received a direct thrombin inhibitor within the last 48 hours; partial thromboplastin time (PTT) > 2.0 times the normal prior to procedure
  • Platelet count < 50,000 mm3
  • Cerebral vasculitis or evidence of active systemic infection
  • Suspicion of aortic dissection, presumed septic embolus, or suspicion of bacterial endocarditis
  • Clinical symptoms suggestive of bilateral stroke or occlusions in multiple vascular territories (e.g., bilateral anterior circulation, or anterior/posterior circulation)
  • Seizure due to stroke
  • Pregnancy
  • Severe contrast allergy or absolute contraindication to iodinated contrast
  • Presence of a carotid artery stenosis or occlusion requiring balloon angioplasty or stenting at time of the procedure
  • Difficult endovascular access or difficult aortic arch or severe neurovascular tortuosity that will result in an inability to deliver endovascular therapy
  • Evidence of dissection in the carotid or target artery for treatment
  • Clinical history, past imaging or clinical judgment suggests that the intracranial occlusion is chronic
  • Active participation in another study involving an investigational drug or device
  • A severe or fatal comorbid illness that will prevent improvement or follow-up or that will render the procedure unlikely to benefit the patient
  • Unwillingness to complete follow up visits

结局指标

主要结局

Symptomatic intracranial haemorrhage rate

时间窗: 36 hours post procedure

Symptomatic intracranial haemorrhage (ICH) as detected by CT/MRI and a clinical deterioration of NIHSS change ≥ 4

Successful revascularization rate

时间窗: Procedure end

Successful revascularization defined at modified Treatment in Cerebral Ischemia (mTICI) 2b-3 at the end of the procedure

次要结局

  • Successful revascularization rate on the first attempt with study device(Procedure)
  • ENT rate(Procedure)
  • Procedure Time(Procedure)
  • Mortality(90 days post procedure)
  • Successful revascularization rate with study device(Procedure)
  • Procedure Complications(Procedure through 90 days)
  • Good functional outcome(90 days post procedure)
  • ICH(36 hours post procedure)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (16)

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