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See also:

  • All acute coronary syndrome clinical trials
  • All clinical trials of antithrombotics
  • All clinical trials of aspirin
  •  

    VA-pilot study, 0

    unpublished (or not yet fully published) trial

    Treatments

    Studied treatment Aspirin 324 mg/d
    Control treatment

    Patients

    Method and design

    Randomized effectives 26 / 24 (studied vs. control)
    Follow-up duration 3m


    Results

    Endpoint Studied treat.
    n/N
    Control treat.
    n/N
    Graph RR [95% CI]

    Non fatal MI

    0 / 26
    1 / 24
    classic 0,18 [0,00;13,05]

    Vascular death

    1 / 26
    3 / 24
    classic 0,31 [0,03;2,76]

    Non vascular death

    0 / 26
    0 / 24
    classic 0,92 [0,00;229,49]

    Non fatal stroke

    0 / 26
    0 / 24
    classic 0,92 [0,00;229,49]

    Vascular events

    1 / 26
    4 / 24
    0,23 [0,03;1,92]

    Major bleeding

    0 / 26
    0 / 24
    classic 0,92 [0,00;229,49]
    0 2 1.0

    Relative risks
    Endpoint Events (%) Relative Risk 95% CI Endpoint definition
    in the trial
    Ref
    Studied treat. Control treat.
    Non fatal MI 0 / 26 (1,9%) 1 / 24 (4,2%) 0,46 [0,02;13,14]    
    Vascular death 1 / 26 (3,8%) 3 / 24 (12,5%) 0,31 [0,03;2,76]    
    Non vascular death 0 / 26 (1,9%) 0 / 24 (2,1%) 0,92 [0,02;44,72]    
    Non fatal stroke 0 / 26 (1,9%) 0 / 24 (2,1%) 0,92 [0,02;44,72]    
    Vascular events 1 / 26 (3,8%) 4 / 24 (16,7%) 0,23 [0,03;1,92]    
    Major bleeding 0 / 26 (1,9%) 0 / 24 (2,1%) 0,92 [0,02;44,72]    
    The primary endpoint (if exists) appears in blod characters
    Reference(s) used for data extraction:
  • 0:

  • Endpoint studied treat. control treat. mean diff

    Absolute risk reduction
    Endpoint Events rate Absolute risk
    reduction (ARR)
    Studied treat. Control treat.
    Vascular death 3,85% 12,50% -86,5‰
    Vascular events 3,85% 16,67% -128,2‰


    Reference(s)

    unpublished (or not yet fully published) trial

    Trials register # NA

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