WebTARDIS was an international prospective randomised open-label blinded-endpoint controlled trial. Patients with acute (<48 hours) non-cardioembolic IS or TIA were ... trial is registered with ClinicalTrials.gov, number NCT00103948. Results: 329 participants were randomly assigned to receive nimodipine and 325 to receive placebo. 476 WebTARDIS is the only large trial of intensive antiplatelets testing the combination of three agents. Intensive antiplatelet therapy with three drugs did not reduce the incidence and …
Triple versus guideline antiplatelet therapy to prevent
WebThe TARDIS trial was an international Prospective Randomised Open-label Blinded End point (PROBE) study that recruited from 106 sites in four countries (Denmark, Georgia, New Zealand and the UK). The protocol can … WebTardis, or “The Tardis,” is a sativa-dominant strain with far-out cerebral effects. Appropriating the title of Dr. Who’s famous phone booth, Tardis is a cross of Oregon … saica headquarters
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WebBackground . The TARDIS trial assessed the safety and efficacy of intensive versus guideline antiplatelet agents given for one month in patients with acute stroke or TIA. The aim of this substudy was to assess the effect of antiplatelet agents taken at baseline on platelet function reactivity and activation. Methods . Platelet function, assessed by … WebNov 4, 2016 · TARDIS is the first trial to assess the safety and efficacy of intensive antiplatelet therapy based on three agents in comparison with guideline treatment; with 3096 patients, TARDIS is a large international trial. The characteristics of the participants justify several comments. WebFeb 28, 2024 · TARDIS Investigators. Antiplatelet therapy with aspirin, clopidogrel, and dipyridamole versus clopidogrel alone or aspirin and dipyridamole in patients with acute cerebral ischaemia (TARDIS): a randomised, open-label, phase 3 superiority trial. Lancet 2024; 391: 850-9. doi: 10.1016/S0140-6736(17)32849-0 pmid: 29274727 saica pack livingston address