CTIS2022-502878-16-00进行中(未招募)1 期
Safety and Efficacy of intra-arterial Tenecteplase for non-complete reperfusion of intracranial occlusion
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 10
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 65+(—)
- 性别
- All
入选标准
- •Informed consent, Age =18 years, Clinical signs consistent with an acute ischemic stroke, Patient had an initial large vessel occlusion in the anterior circulation defined as intracranial ICA, M1, M2, M3, A1, A2, P1 or P2, Patient has undergone endovascular stroke treatment, Onset to randomization no later than < 705 minutes (11h 45min) after symptom-onset/last-seen well., Incomplete reperfusion defined as any of the following: a. For ICA/M1: TICI2b/2c (50-99%) reperfusion after endovascular treatment without mechanically amendable target-occlusion (as per definition by the interventionalist). b. For A1/A2, P1/P2, M2/M3: TICI2a/2b/2c (1-99%) reperfusion after endovascular treatment without mechanically amendable target-occlusion (as per definition by the interventionalist). c. Any emboli to the new territory without mechanically amendable target-occlusion (as per definition by the interventionalist)., Signs of early ischemic changes of non-contrast CT Alberta Stroke Program Early CT Score (ASPECTS) =5 (for DWI-ASPECTS = 4, for DWI-ASECTS: a region must have diffusion abnormality in 20% or more of its volume to be considered DWI-ASPECTS positive)
排除标准
- •Acute intracranial hemorrhage, Radiological confirmed evidence of mass effect or intracranial tumor (except small meningioma), Radiological confirmed evidence of cerebral vasculitis, Contraindication to MRI (e.g. pacemaker), Pregnancy or lactating women, Any severe bleeding within the past 6 months, which would prevent administration of intravenous thrombolysis in clinical routine, Major surgery in the past 2 months with severe risk of bleeding which would prevent administration of intravenous thrombolysis in clinical routine, Intake of Vitamin K antagonista with INR >1.7, Platelets < 50,000, Non-controlled hypertension (defined as SBP >185 mmHg or DBP >110 mmHg refractory to treatment), Calcified thrombi, Active dyspeptic ulcer, Acute endocarditis, Known arterial aneurysm, Known neoplasms with risk of bleeding, Severe liver fibrosis or portal hypertension, Acute pericarditis, Acute pancreatitis, Known allergy to TNK or Gentamicin or other additives/auxiliaries (Polysorbatum 20, L-Argininum, Acidum phosphoricum), Known Renal failure either as defined by a serum creatinine > 3.0 mg/dl (or 265.2 µmol/l) or glomerular Filtration Rate [GFR] < 30 or as subject who required hemodialysis/peritoneal dialysis
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