NL-OMON56450尚未招募不适用
EnDovascular therapy plus best medical treatment (BMT) versus BMT alone for MedIum VeSsel Occlusion sTroke - a prAgmatic, international, multicentre, randomized triaL (DISTAL) - DISTA
niversity Hospital Basel0 个研究点目标入组 100 人开始时间: 待定最近更新:
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
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •1. Acute ischemic stroke
- •2. Treatment (arterial puncture) can be initiated
- •2.1. Within 6 hours of last seen well (LSW)
- •2.2. Within 6 to 24 hours of LSW AND
- •CT Criteria: Evidence of a hypoperfusion-hypodensity mismatch (Absence of
- •hypodensity on the non-contrast CT within >= 90% of the area of the hypoperfused
- •lesion on perfusion CT)
- •MRI Criteria: Evidence of a diffusion-hyperintensity mismatch (Absence of
- •hyperintensity on fluid-attenuated inversion recovery (FLAIR) imaging within >=
- •90% of the area of the diffusion weighted imaging (DWI) lesion)
- •3. Isolated medium vessel occlusion (i.e. an occlusion of the co-/non-dominant
- •M2, the M3/M4 segment of the MCA, the A1/A2/A3 segment of the ACA or the P1/P2
- •segment of the PCA) confirmed by CT or MRI Angiography
- •4. National Institute of Health Stroke Scale (NIHSS) Score of >= 4 points or
- •symptoms deemed clearly disabling by treating physician (i.e. aphasia,
- •hemianopia, etc.)
- •5. Age >=18 years
- •6. Deferred Written informed consent.
- •7. Agreement of treating physician to perform endovascular procedure
排除标准
- •1. Acute intracranial haemorrhage
- •2. Patient bedridden or presenting from a nursing home
- •3. In-Hospital Stroke
- •4. Known (serious) sensitivity to radiographic contrast agents, nickel,
- •titanium metals or their alloys
- •5. Foreseeable difficulties in follow-up due to geographic reasons (e.g.
- •patients living abroad)
- •6. Evidence of an ongoing pregnancy prior to randomization. A negative
- •pregnancy test before randomisation is required for all women with
- •child-bearing potential.
- •7. Known history of arterial tortuosity, pre-existing stent, other arterial
- •disease and/or known disease at the arterial access site that would prevent the
- •device from reaching the target vessel and/or preclude safe recovery after EVT
- •8. Known, severe comorbidities, which will likely prevent improvement or
- •follow-up (active cancer, alcohol/drug abuse or dementia)
- •9. Radiological confirmed evidence of mass effect or intracranial tumour
- •(except small meningioma)
- •10. Radiological confirmed evidence of cerebral vasculitis
- •11. Evidence of vessel recanalization prior to randomisation
- •12. Participation in another interventional trial
研究者
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