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dc.contributor.authorFox, K.
dc.contributor.authorRothwell, P. M.
dc.contributor.authorFisher, M.
dc.contributor.authorFord, I.
dc.contributor.authorHennerici, M. G.
dc.contributor.authorMattle, H. P.
dc.contributor.authorBousser, M. G.
dc.contributor.authorAmarenco, P.
dc.contributor.authorChamorro, A.
dc.date.accessioned2021-03-05T11:50:53Z
dc.date.available2021-03-05T11:50:53Z
dc.date.issued2009
dc.identifier.citationBousser M. G. , Amarenco P., Chamorro A., Fisher M., Ford I., Fox K., Hennerici M. G. , Mattle H. P. , Rothwell P. M. , "Rationale and Design of a Randomized, Double-Blind, Parallel-Group Study of Terutroban 30 mg/day versus Aspirin 100 mg/day in Stroke Patients: The Prevention of Cerebrovascular and Cardiovascular Events of Ischemic Origin with Terutroban in Patients with a History of Ischemic Stroke or Transient Ischemic Attack (PERFORM) Study", CEREBROVASCULAR DISEASES, cilt.27, ss.509-518, 2009
dc.identifier.issn1015-9770
dc.identifier.othervv_1032021
dc.identifier.otherav_aa30b883-f8eb-4aed-bdab-54cd7acb63f9
dc.identifier.urihttp://hdl.handle.net/20.500.12627/113648
dc.identifier.urihttps://doi.org/10.1159/000212671
dc.description.abstractBackground: Ischemic stroke is the leading cause of mortality worldwide and a major contributor to neurological disability and dementia. Terutroban is a specific TP receptor antagonist with antithrombotic, antivasoconstrictive, and antiatherosclerotic properties, which may be of interest for the secondary prevention of ischemic stroke. This article describes the rationale and design of the Prevention of cerebrovascular and cardiovascular Events of ischemic origin with teRutroban in patients with a history oF ischemic strOke or tRansient ischeMic Attack (PERFORM) Study, which aims to demonstrate the superiority of the efficacy of terutroban versus aspirin in secondary prevention of cerebrovascular and cardiovascular events. Methods and Results: The PERFORM Study is a multicenter, randomized, double-blind, parallel-group study being carried out in 802 centers in 46 countries. The study population includes patients aged 6 55 years, having suffered an ischemic stroke (<= 3 months) or a transient ischemic attack (<= 8 days). Participants are randomly allocated to terutroban (30 mg/day) or aspirin (100 mg/ day). The primary efficacy endpoint is a composite of ischemic stroke (fatal or nonfatal), myocardial infarction (fatal or nonfatal), or other vascular death (excluding hemorrhagic death of any origin). Safety is being evaluated by assessing hemorrhagic events. Follow-up is expected to last for 2-4 years. Assuming a relative risk reduction of 13%, the expected number of primary events is 2,340. To obtain statistical power of 90%, this requires inclusion of at least 18,000 patients in this event-driven trial. The first patient was randomized in February 2006. Conclusions: The PERFORM Study will explore the benefits and safety of terutroban in secondary cardiovascular prevention after a cerebral ischemic event. Copyright (C) 2009 S. Karger AG, Basel
dc.language.isoeng
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectPERİFERAL VASKÜLER HASTALIĞI
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleRationale and Design of a Randomized, Double-Blind, Parallel-Group Study of Terutroban 30 mg/day versus Aspirin 100 mg/day in Stroke Patients: The Prevention of Cerebrovascular and Cardiovascular Events of Ischemic Origin with Terutroban in Patients with a History of Ischemic Stroke or Transient Ischemic Attack (PERFORM) Study
dc.typeMakale
dc.relation.journalCEREBROVASCULAR DISEASES
dc.contributor.departmentAssistance Publique Hopitaux Paris (APHP) , ,
dc.identifier.volume27
dc.identifier.issue5
dc.identifier.startpage509
dc.identifier.endpage518
dc.contributor.firstauthorID90082


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