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6篇 您的检索式:作者名="Fergus Doubal"
    题名 作者 年代 出处 被引量
1Enlarged Perivascular Spaces on MRI Are a Feature of Cerebral Small Vessel Disease显示文摘Fergus N. Doubal Alasdair M.J. MacLullich Karen J. Ferguson Martin S. Dennis Joanna M. Wardlaw 2010Stroke2010,,:1
2Counting Cavitating Lacunes Underestimates the Burden of Lacunar Infarction显示文摘Gillian M. Potter Fergus N. Doubal Caroline A. Jackson Francesca M. Chappell Cathie L. Sudlow Martin S. Dennis Joanna M. Wardlaw 2010Stroke2010,,2:1
3Blood-brain barrier permeability and long term clinical and imaging outcomes in cerebral small vessel disease显示文摘Joanna M Wardlaw Fergus N Doubal Maria Valdes-Hernandez 2013Stroke2013,44,2:1
4Blood-brain barrier permeability and long term clinical and imaging outcomes in cerebral small vessel disease显示文摘Joanna M Wardlaw Fergus N Doubal Maria Valdes-Hernandez 2013Stroke2013,44,2:1
5Enlarged Perivascular Spaces on MRI Are a Feature of Cerebral Small Vessel Disease显示文摘Fergus N. Doubal Alasdair M.J. MacLullich Karen J. Ferguson Martin S. Dennis Joanna M. Wardlaw 2010Stroke2010,,3:1
6Cilostazol and isosorbide mononitrate for the prevention of progression of cerebral small vessel disease:baseline data and statistical analysis plan for the Lacunar Intervention Trial-2(LACI-2)(ISRCTN14911850)显示文摘Background Cerebral small vessel disease(SVD)causes lacunar strokes(25%of all ischaemic strokes),physical frailty and cognitive impairment and vascular and mixed dementia.There is no specific treatment to prevent progression of SVD.Methods The LACunar Intervention Trial-2 is an investigator-initiated prospective randomised open-label blinded-endpoint phase II feasibility study assessing cilostazol and isosorbide mononitrate for preventing SVD progression.We aimed to recruit 400 patients with clinically evident lacunar ischaemic stroke and randomised to cilostazol,isosorbide mononitrate,both or neither,in addition to guideline secondary ischaemic stroke prevention,in a partial factorial design.The primary outcome is feasibility of recruitment and adherence to medication;key secondary outcomes include:drug tolerability;recurrent vascular events,cognition and function at 1 year after randomisation;and safety(bleeding,falls,death).Data are number(%)and median(IQR).Results The trial commenced on 5 February 2018 and ceased recruitment on 31 May 2021 with 363 patients randomised,with the following baseline characteristics:average age 64(56.0,72.0)years,female 112(30.9%),stroke onset to randomisation 79.0(27.0,244.0)days,hypertension 267(73.6%),median blood pressures 143.0(130.0,157.0)/83.0(75.0,90.0)mm Hg,current smokers 67(18.5%),educationally achieved end of school examinations(A-level)or higher 118(32.5%),modified Rankin scale 1.0(0.0,1.0),National Institutes Health stroke scale 1.0(1.4),Montreal Cognitive Assessment 26.0(23.0,28.0)and total SVD score on brain imaging 1.0(0.0,2.0).This publication summarises the baseline data and presents the statistical analysis plan.Summary The trial is currently in follow-up which will complete on 31 May 2022 with results expected in October 2022.Trial registration number ISRCTN14911850.Philip M Bath Iris Mhlanga Lisa J Woodhouse Fergus Doubal Katherine Oatey Alan A Montgomery Joanna M Wardlaw LACI-Trial Investigators 2023Stroke & Vascular Neurology2023,8,2:0
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