首页> 外文期刊>Lancet Neurology >Effects of aspirin plus extended-release dipyridamole versus clopidogrel andtelmisartan on disability and cognitive function after recurrent stroke in patients with ischaemic stroke in the Prevention Regimen for Effectively Avoiding Second Strokes (PRoFESS) trial: a double-blind, active and placebo-controlled study
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Effects of aspirin plus extended-release dipyridamole versus clopidogrel andtelmisartan on disability and cognitive function after recurrent stroke in patients with ischaemic stroke in the Prevention Regimen for Effectively Avoiding Second Strokes (PRoFESS) trial: a double-blind, active and placebo-controlled study

机译:在有效避免二次卒中预防方案(PRoFESS)试验中,阿司匹林加缓释双嘧达莫与氯吡格雷和替米沙坦对缺血性卒中患者复发性卒中后残疾和认知功能的影响:一项双盲,积极,安慰剂对照研究

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Summary:Background The treatment of ischaemic stroke with neuroprotective drugs has been unsuccessful, and whether these compounds can be used to reduce disability after recurrent stroke is unknown. The putative neuroprotective effects of antiplatelet compounds and the angiotensin II receptor antagonist telmisartan were investigated in the Prevention Regimen for Effectively Avoiding Second Strokes (PRoFESS) trial.Methods Patients who had had an ischaemic stroke were randomly assigned in a twojjy two factorial design to receive either 25 mg aspirin (ASA) and 200 mg extended-release dipyridamole (ER-DP) twice a day or 75 mg clopidogrel once a day, and either 80 mg telmisartan or placebo once per day. The predefined endpoints for this substudy were disability after a recurrent stroke, assessed with the modified Rankin scale (mRS) and Barthel index at 3 months, and cognitive function, assessed with the mini-mental state examination (MMSE) score at 4 weeks after randomisation and at the penultimate visit. Analysis was by intention to treat. The study was registered with ClinicalTrials.gov, number NTC00153062.
机译:摘要:背景使用神经保护药治疗缺血性中风一直未成功,这些化合物是否可用于减少复发性中风后的残疾尚不清楚。在有效避免第二次中风预防方案(PRoFESS)试验中,研究了抗血小板化合物和血管紧张素II受体拮抗剂替米沙坦的假定神经保护作用。每天两次25毫克阿司匹林(ASA)和200毫克缓释双嘧达莫(ER-DP)或每天一次75毫克氯吡格雷,每天一次80毫克替米沙坦或安慰剂。该子研究的预定义终点是卒中后的残疾,在3个月时用改良的Rankin量表(mRS)和Barthel指数评估,认知功能在随机化后4周时用小精神状态检查(MMSE)评分评估并进行倒数第二次访问。分析是按意向进行的。该研究已在ClinicalTrials.gov上注册,编号为NTC00153062。

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