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Related trials

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See also:

  • All venous thrombosis clinical trials
  •  

    Lopaciuk study, 3000

    Treatments

    Studied treatment subcutaneous sodic heparin 34 400 U daily (mean)
    Control treatment intravenous sodic heparin 37 000 U daily (mean)

    Patients

    Method and design

    Randomized effectives 48 / 46 (studied vs. control)


    Results

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

    Recurrent thromboembolic event

    2 / 48
    7 / 46
    0,27 [0,06;1,25]

    Major bleeding

    2 / 48
    1 / 46
    classic 1,92 [0,18;20,43]
    0 2 1.0

    Relative risks
    Endpoint Events (%) Relative Risk 95% CI Endpoint definition
    in the trial
    Studied treat. Control treat.
    Recurrent thromboembolic event 2 / 48 (4,2%) 7 / 46 (15,2%) 0,27 [0,06;1,25]  
    Major bleeding 2 / 48 (4,2%) 1 / 46 (2,2%) 1,92 [0,18;20,43]  
    The primary endpoint (if exists) appears in blod characters

    Endpoint studied treat. control treat. mean diff

    Absolute risk reduction
    Endpoint Events rate Absolute risk
    reduction (ARR)
    Studied treat. Control treat.
    Recurrent thromboembolic event 4,17% 15,22% -110,5‰
    Major bleeding 4,17% 2,17% 2,0%


    Reference(s)

    Trials register # NA

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