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dc.contributor.authorLarsen, Kristin Tveitan
dc.contributor.authorForfang, Elisabeth
dc.contributor.authorPennlert, Johanna
dc.contributor.authorGlader, Eva-Lotta
dc.contributor.authorKruuse, Christina
dc.contributor.authorWester, Per
dc.contributor.authorIhle-Hansen, Hege
dc.contributor.authorCarlsson, Maria
dc.contributor.authorBerge, Eivind
dc.contributor.authorAl-Shahi Salman, Rustam
dc.contributor.authorWyller, Torgeir Bruun
dc.contributor.authorRønning, Ole M.
dc.date.accessioned2021-04-15T13:57:42Z
dc.date.available2021-04-15T13:57:42Z
dc.date.issued2020-09-03
dc.description.abstractBackground and aims - Many patients with prior intracerebral haemorrhage have indications for antithrombotic treatment with antiplatelet or anticoagulant drugs for prevention of ischaemic events, but it is uncertain whether such treatment is beneficial after intracerebral haemorrhage. STudy of Antithrombotic Treatment after IntraCerebral Haemorrhage will assess (i) the effects of long-term antithrombotic treatment on the risk of recurrent intracerebral haemorrhage and occlusive vascular events after intracerebral haemorrhage and (ii) whether imaging findings, like cerebral microbleeds, modify these effects.<p> <p>Methods - STudy of Antithrombotic Treatment after IntraCerebral Haemorrhage is a multicentre, randomised controlled, open trial of starting versus avoiding antithrombotic treatment after non-traumatic intracerebral haemorrhage, in patients with an indication for antithrombotic treatment. Participants with vascular disease as an indication for antiplatelet treatment are randomly allocated to antiplatelet treatment or no antithrombotic treatment. Participants with atrial fibrillation as an indication for anticoagulant treatment are randomly allocated to anticoagulant treatment or no anticoagulant treatment. Cerebral CT or MRI is performed before randomisation. Duration of follow-up is at least two years. The primary outcome is recurrent intracerebral haemorrhage. Secondary outcomes include occlusive vascular events and death. Assessment of clinical outcomes is performed blinded to treatment allocation. Target recruitment is 500 participants.en_US
dc.identifier.citationLarsen, Forfang, Pennlert, Glader, Kruuse, Wester, Ihle-Hansen, Carlsson, Berge, Al-Shahi Salman, Wyller, Rønning. STudy of Antithrombotic Treatment after IntraCerebral Haemorrhage: Protocol for a randomised controlled trial. European Stroke Journal. 2020;5(4):414-422
dc.identifier.cristinIDFRIDAID 1887834
dc.identifier.doi10.1177/2396987320954671
dc.identifier.issn2396-9873
dc.identifier.issn2396-9881
dc.identifier.urihttps://hdl.handle.net/10037/20899
dc.language.isoengen_US
dc.publisherSAGE Publicationsen_US
dc.relation.journalEuropean Stroke Journal
dc.rights.holderCopyright 2020 The Author(s)en_US
dc.subjectVDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710en_US
dc.subjectVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710en_US
dc.titleSTudy of Antithrombotic Treatment after IntraCerebral Haemorrhage: Protocol for a randomised controlled trialen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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