SYNTHESIS Expansion: design of a nonprofit, pragmatic, randomized, controlled trial on the best fast-track endovascular treatment vs. standard intravenous alteplase for acute ischemic stroke

被引:14
作者
Ciccone, Alfonso [1 ]
Valvassori, Luca [2 ]
Nichelatti, Michele [3 ]
机构
[1] Osped Niguarda Ca Granda, Dept Neurosci, Stroke Unit, I-20164 Milan, Italy
[2] Osped Niguarda Ca Granda, Dept Neurosci, Neurointervent Unit, I-20164 Milan, Italy
[3] Osped Niguarda Ca Granda, Serv Biostat, I-20164 Milan, Italy
关键词
catheter-based treatment; cerebral infarction; cerebrovascular accident; clinical trials; endovascular treatment; interventional radiology; intra-arterial alteplase; intravenous alteplase; randomized-controlled trial; stroke; TISSUE-PLASMINOGEN-ACTIVATOR; CEREBRAL-ARTERY STROKE; THROMBOLYTIC THERAPY; INTRAARTERIAL; OCCLUSION; PROUROKINASE; PROACT; SIGN;
D O I
10.1111/j.1747-4949.2011.00587.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rationale Reperfusion in ischemic stroke can be pursued by either systemic intravenous thrombolysis or endovascular treatment. However, systemic intravenous thrombolysis with alteplase within 4 center dot 5 h of symptom onset in selected patients is the only medication of proven efficacy. No randomized-controlled trials have so far compared the two modalities. To explore this, after a pilot phase, we started the SYNTHESIS Expansion trial. Aims To determine whether endovascular treatment (i.e., intra-arterial thrombolysis with alteplase - if necessary, associated to or substituted by mechanical clot disruption and/or retrieval) compared with systemic intravenous thrombolysis with alteplase, administered according to European labelling, increases the proportion of independent survivors at three-months. Design SYNTHESIS Expansion is an open-label, multicenter randomized-controlled trial, with blinded follow-up. Eligibility applies to; patients with symptomatic ischemic stroke, seen within 4 center dot 5 h of onset; being able to initiate intravenous alteplase immediately, and endovascular treatment as soon as possible (not later than six-hours of stroke onset). The study is pragmatically based on the 'uncertainty principle' between endovascular treatment and systemic intravenous thrombolysis for patients eligible for intravenous alteplase. There are no prespecified clinical or instrumental criteria to further select a patient, although investigators are left free to use them. Enrollment will be completed with 350 randomized patients. Primary analysis is on an intent-to-treat basis. Study outcomes Primary: modified Rankin scale score of 0 or 1 at three-months. Secondary: neurological deficit seven-days after thrombolysis and the safety of the procedure on the basis of events reported within seven-days following thrombolysis - symptomatic cerebral hemorrhage, fatal and nonfatal stroke, death from any cause, neurological deterioration.
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收藏
页码:259 / 265
页数:7
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