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  • CAPTIVA

    The primary goal of the trial is to determine if the experimental arms (rivaroxaban or ticagrelor or both) are superior to the clopidogrel arm for lowering the 1-year rate of ischemic stroke, intracerebral hemorrhage, or vascular death.

    Investigator
    Anna Y Khanna
    Ages
    30 Years - N/A
    Sexes
    All
  • CAPTIVA

    The primary goal of the trial is to determine if the experimental arms (rivaroxaban or ticagrelor or both) are superior to the clopidogrel arm for lowering the 1-year rate of ischemic stroke, intracerebral hemorrhage, or vascular death.

    Investigator
    Brian L Hoh
    Ages
    30 Years - N/A
    Sexes
    All
  • Sleep SMART

    The purpose of this study is to determine whether treatment of obstructive sleep apnea (OSA) with positive airway pressure starting shortly after acute ischemic stroke (1) reduces recurrent stroke, acute coronary syndrome, and all-cause mortality 6鈥�

    Investigator
    Anna Y Khanna
    Ages
    18 Years - N/A
    Sexes
    All
  • LIBREXIA-ACS

    The purpose of this study is to evaluate if milvexian is at least as effective as apixaban for reducing the risk of the composite stroke and non-central nervous system (CNS) systemic embolism.

    Investigator
    Carl J Pepine
    Ages
    18 Years - N/A
    Sexes
    All
  • Librexia AF

    The purpose of this study is to evaluate if milvexian is at least as effective as apixaban for reducing the risk of the composite stroke and non-central nervous system (CNS) systemic embolism.

    Investigator
    Mohammed Ruzieh
    Ages
    18 Years - N/A
    Sexes
    All
  • FASTEST Trial

    The objective of the rFVIIa for Acute Hemorrhagic Stroke Administered at Earliest Time (FASTEST) Trial is to establish the first treatment for acute spontaneous intracerebral hemorrhage (ICH) within a time window and subgroup of patients that is鈥�

    Investigator
    Anna Y Khanna
    Ages
    18 Years - 80 Years
    Sexes
    All
  • Gaucher Disease Registry

    The ICGG Gaucher Registry is an ongoing, international multi-center, strictly observational program that tracks the routine clinical outcomes for patients with Gaucher disease, irrespective of treatment status. No experimental intervention is鈥�

    Ages
    N/A - N/A
    Sexes
    All