TARDISSafety and Efficacy of Intensive Versus Guideline Antiplatelet Therapy in High Risk Patients With Recent Ischaemic Stroke or Transient Ischaemic Attack: a Randomised Controlled Trial

Study start date: April 1, 2009

Inclusion Criteria: Adults at high risk of recurrent ischaemic stroke: Age ≥ 50 years Within 48 hours of ictus (24-48 hours if thrombolysed) TIA with limb weakness and/or dysphasia lasting between 10 minutes and < 24 hours with no residual symptoms and presenting with any of the following ABCD2 score > 4, or Crescendo TIA or Already on dual antiplatelet therapy Note: Neuroimaging is not necessary for transient ischaemic attack. Crescendo TIA is > 1 TIA in one week and the onset time of last TIA is taken as time of ictus. Ischaemic non cardioembolic stroke presenting with any of the following Ongoing limb weakness and/or dysphasia of more than one hour duration Resolved limb weakness of more than one hour duration with ongoing facial weakness Ongoing isolated hemianopia of more than 1 hour duration with positive neuroimaging evidence to support the index event (e.g. ischaemic stroke in occipital lobe) Resolved limb weakness and/or dysphasia between 24-48 hours after index event onset Note: Neuroimaging is essential for ischaemic stroke to exclude intracranial haemorrhage and/or non stroke diagnosis Informed consent from participant. If the participant is unable to give meaningful consent e.g. due to dysphasia, confusion, or reduced conscious level, proxy consent may be obtained from a relative, carer or legal representative. Exclusion Criteria: Age < 50 Isolated sensory symptoms or vertigo/dizziness or facial weakness Isolated hemianopia without positive neuroimaging evidence Intracranial haemorrhage Baseline neuroimaging showing parenchymal haemorrhagic transformation (PH I/II) of infarct, subarachnoid haemorrhage or other non ischaemic cause for symptoms Presumed cardioembolic stroke (e.g. history or current AF, myocardial infarction within 3 months) Participants with contraindications to, or intolerance of, aspirin, clopidogrel or dipyridamole. Participants with definite need for treatment with aspirin, clopidogrel or dipyridamole individually or in combination (e.g. aspirin and clopidogrel for recent MI/acute coronary syndrome) Participant has taken clopidogrel or dipyridamole after the index event but prior to randomisation (aspirin is allowed between ictus onset and randomisation) Definite need for full dose oral (e.g. warfarin, dabigatran) or medium to high dose parenteral (e.g. heparin) anti-coagulation. NB Low dose heparin for DVT prophylaxis is allowed Definite need for glycoprotein IIb-IIIa inhibitors Received thrombolysis within the last 24 hours No enteral access Pre-morbid dependency (mRS > 2). Severe high BP (BP > 185/110 mmHg). Haemoglobin less than 10g/dL Platelet count more than 600 x 109 /L or less than 100 x 109 /L White cell count more than 30 x 109 /L or less than 3.5 x 109 /L Major bleeding within 1 year (e.g. peptic ulcer, intracerebral haemorrhage). Planned surgery during 3 month follow-up (e.g. carotid endarterectomy) Concomitant STEMI or NSTEMI. Stroke secondary to a procedure (e.g. carotid or coronary intervention) Coma (GCS < 8) Non-stroke life expectancy < 6 months Dementia Participation in another drug or devices trial concurrently or within 30 days. (participants may take part in observational studies or non-drug or devices trials) Geographical or other factors that may interfere with follow-up e.g. no fixed address or telephone contact number, not registered with a GP, or overseas visitor. Females of childbearing potential, pregnancy or breastfeeding