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Related trials

BASKET-PROVE (SES), 2010 - sirolimus eluting stent vs bare-metal stent

SPIRIT IV, 2010 - everolimus eluting stent vs paclitaxel eluting stent

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BASKET-PROVE (EES), 2010 - everolimus eluting stent vs bare-metal stent

ISAR TEST 3 (BP), 2009 - sirolimus biodegradable polymer vs sirolimus eluting stent

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Juwana, 2009 - sirolimus eluting stent vs paclitaxel eluting stent

DEBATER (SES vs BMS), 2009 - sirolimus eluting stent vs bare-metal stent

ISAR TEST 2 (vs ZES), 2009 - dual sirolimus, probucol eluting stent vs zotarolimus eluting stent

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ENDEAVOR IV, 2009 - zotarolimus eluting stent vs paclitaxel eluting stent

BARI 2D, 2009 - CABG or PCI vs medical treatment

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ISAR-TEST-4 (biodegradable polymer), 2009 - sirolimus biodegradable polymer vs sirolimus eluting stent

PASEO, 2009 - drug-eluting stents vs bare-metal stent

COMPARE, 2009 - everolimus eluting stent vs paclitaxel eluting stent

ISAR TEST 2 (vs SES), 2009 - dual sirolimus, probucol eluting stent vs sirolimus eluting stent

ISAR TEST 3 (PF), 2009 - polymer free sirolimus stent vs sirolimus eluting stent



See also:

  • All acute myocardial infarction clinical trials
  • All coronary artery disease clinical trials
  • All clinical trials of PCI
  • All clinical trials of paclitaxel eluting stent
    		•  

    HAAMU-STENT study, 2006

    unpublished (or not yet fully published) trial Facebook    pdf : paclitaxel eluting stent - myocardial revascularization for coronary artery disease

    Treatments

    Studied treatment Taxus Express
    Control treatment Bare-metal-stent
    Concomittant treatment After PCI, patients were treated with a 300- to 600-mg loading dose of clopidogrel, followed by clopidogrel 75 mg daily for one year

    Patients

    Patients AMI - STEMI patients undergoing PCI
    Baseline characteristics
    age 63 
    diabetes (%) 15% 
    Lesion diameter inclusion criteria NA 
    Female (%) 28% 

    Method and design

    Randomized effectives 70 / 75 (studied vs. control)
    Design Parallel groups
    Blinding open
    Follow-up duration 12 months
    Number of centre 1
    Geographic area Finland
    Primary endpoint none


    Results

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

    All cause death

    8 / 70
         4 / 75
         classic 2,14 [0,67;6,80]

    angiographic restenosis

    NA / 70
         NA / 75

    Stent thrombosis (any, end of follow up)

    1 / 70
         3 / 75
         classic 0,36 [0,04;3,35]     0 2 1.0

    Relative risks
    Endpoint Events (%) Relative Risk 95% CI Endpoint definition
    in the trial    		 Ref
    Studied treat. Control treat.
    All cause death 8 / 70 (11,4%) 4 / 75 (5,3%) 2,14 [0,67;6,80]    
    Stent thrombosis (any, end of follow up) 1 / 70 (1,4%) 3 / 75 (4,0%) 0,36 [0,04;3,35]    
    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.
    All cause death 11,43% 5,33% 6,1%
    Stent thrombosis (any, end of follow up) 1,43% 4,00% -25,7‰

    Meta-analysis of all similar trials:

    Drug eluting stent in coronary artery disease for all type of patients

    Drug eluting stent in coronary artery disease for acute myocardial infarction

    myocardial revascularization in acute myocardial infarction for all type of patients

    myocardial revascularization in coronary artery disease for all type of patient

    PCI in acute myocardial infarction for all type of patients



    Reference(s)

    Trials register # NA

    unpublished (or not yet fully published) trial

    • Tierala I, Syvaenne M, Kupari M. Randomised comparison of apaclitaxel-eluting and a bare metal stent in STEMI-PCI. TheHAAMU-STENT-study. Annual Scientifi c Meeting of theTranscatheter Cardiovascular Therapeutics; Washington, DC;Oct 2227, 2006. Abstract 178.
      Pubmed | Hubmed | Fulltext

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