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Status: Bibliographieeintrag

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Verfasst von:Bousser, Marie-Germaine [VerfasserIn]   i
 Amarenco, P. [VerfasserIn]   i
 Chamorro, A. [VerfasserIn]   i
 Fisher, M. [VerfasserIn]   i
 Ford, I. [VerfasserIn]   i
 Fox, K. [VerfasserIn]   i
 Hennerici, Michael G. [VerfasserIn]   i
 Mattle, H. P. [VerfasserIn]   i
 Rothwell, P. M. [VerfasserIn]   i
Titel:Rationale and design of a randomized, double-blind, parallel-group study of terutroban 30 mg/day versus aspirin 100 mg/day in stroke patients
Titelzusatz: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
Verf.angabe:M.G. Bousser, P. Amarenco, A. Chamorro, M. Fisher, I. Ford, K. Fox, M.G. Hennerici, H.P. Mattle, P.M. Rothwell, on behalf of the PERFORM Study Investigators
E-Jahr:2009
Jahr:April 16, 2009
Umfang:10 S.
Fussnoten:Gesehen am 20.04.2022
Titel Quelle:Enthalten in: Cerebrovascular diseases
Ort Quelle:Basel : Karger, 1991
Jahr Quelle:2009
Band/Heft Quelle:27(2009), 5, Seite 509-518
ISSN Quelle:1421-9786
Abstract:BACKGROUND: 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 > or =55 years, having suffered an ischemic stroke (< or =3 months) or a transient ischemic attack (< or =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.
DOI:doi:10.1159/000212671
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1159/000212671
 DOI: https://doi.org/10.1159/000212671
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Aged
 Aged, 80 and over
 Aspirin
 Cardiovascular Diseases
 Dose-Response Relationship, Drug
 Double-Blind Method
 Endpoint Determination
 Female
 Humans
 International Cooperation
 Ischemic Attack, Transient
 Male
 Middle Aged
 Naphthalenes
 Platelet Aggregation Inhibitors
 Propionates
 Receptors, Thromboxane
 Stroke
 Treatment Outcome
K10plus-PPN:1799858707
Verknüpfungen:→ Zeitschrift

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