7 clinical trials found.
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Comparison of Anti-coagulation and anti-Platelet Therapies for Intracranial Vascular Atherostenosis
The purpose of this research study is to see whether ticagrelor and aspirin or rivaroxaban and aspirin compared to clopidogrel and aspirin will have the ...Phase
TRIAL ROLE: Principal Investigator
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Neurological Emergencies Outcomes at NYU
The purpose of this research study is to (1) identify specific findings during the hospitalization and pre- injury that are associated with acquiring a hospital ...Phase N/A TRIAL ROLE: Sub Investigator
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STATINS USE IN INRACEREBRAL HEMORRHAGE PATIENTS (SATURN)
This research is being done to find out if it is better to continue or discontinue statin drugs in people who had a brain hemorrhage ...Phase
TRIAL ROLE: Sub Investigator
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Anticoagulation for Stroke Prevention and Recovery after ICH (ASPIRE)
Survivors of intracerebral hemorrhage (ICH) who have atrial fibrillation (AF) are at high risk for subsequent ischemic stroke. An “ischemic” stroke is an injury to ...Phase
TRIAL ROLE: Sub Investigator
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Sleep for Stroke Management And Recovery Trial (Sleep SMART)
The purpose of the study is to examine if continuous positive airway pressure (CPAP) treatment may improve outcomes after stroke. CPAP might improve your physical ...Phase
TRIAL ROLE: Sub Investigator
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A multicenter international randomized placebo controlled double-blind parallel group and event driven Phase 3 study of the oral FXIa inhibitor asundexian (BAY 2433334) for the prevention of ischemic stroke in male and female participants aged 18 years or older.
OCEANIC-STROKE (study 20604) is a multicenter, international, randomized, placebo controlled, double-blind, parallel group, event driven phase 3 study. The purpose of this study is to ...Phase
TRIAL ROLE: Sub Investigator
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Biomarker and Edema Attenuation in IntraCerebral Hemorrhage (BEACH)
The purpose of this research study is to learn more about the effects of the study drug called MW189 in people who have bleeding in ...Phase
TRIAL ROLE: Sub Investigator
