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Multi-center, Randomized Trial Comparing Dual Antiplatelet Therapy With CILOstazol Plus Aspirin Versus Aspirin Alone Following PERipheral Endovascular Procedures (NCT02770274)

University Hospital of Patras
To compare the safety and effectiveness of dual anti-platelet therapy with cilostazol 100 mg twice daily and aspirin 100 mg daily versus monotherapy with aspirin 100 mg daily in patients undergoing peripheral angioplasty or stenting or both for the management of peripheral arterial disease.
  • Drug: Cilostazol
    Dual therapy with Cilostazol 100 mg twice daily
    • Drug: Aspirin
      Monotherapy with aspirin 100 mg once daily
      Ages eligible for Study
      18 Years to 85 Years
      Genders eligible for Study
      All
      Accepts Healthy Volunteers
      No
      Inclusion Criteria:
      • Scheduled infrainguinal (femoropopliteal or infrapopliteal or both) angioplasty and/or stenting.
      • Surgical or endovascular treatment of Inflow iliac artery significant stenosis if deemed necessary.
      • Symptomatic severe intermittent claudication (Rutherford-Becker 3) or critical limb ischemia (Rutherford-Becker 4-6).
      • Informed consent signed
      Exclusion Criteria:
      • Any contraindication to aspirin or cilostazol intake
      • No pedal arch outflow
      • Sole iliac artery treatment
      • Standard contraindications to angioplasty
      • Acute or sub-acute limb ischemia
      This is a multi-center, randomized, single-blinded, phase III, controlled trial investigating the safety and effectiveness of dual antiplatelet therapy with cilostazol 100 mg twice daily and aspirin 100 mg daily versus monotherapy with aspirin 100 mg daily in patients undergoing peripheral, infrainguinal angioplasty or stenting or both for the management of peripheral arterial disease (intermittent claudication or critical limb ischemia). The study will include in total 200 patients randomized on a 1:1 basis to receive either dual antiplatelet therapy for 6 months cilostazol 100 mg once daily and aspirin 100 mg daily versus monotherapy with aspirin 100 mg daily for 12 months. The study's primary endpoint will be the composite of major adverse cardiovascular events (cardiovascular death, myocardial infarction, stroke, major amputation, target limb open surgical or endovascular revascularization). Additional therapy with clopidogrel 75mg daily will be added in either group for one month in case of stent placement. Secondary endpoints will include quality of life assessment using dedicated questionnaires, drug- and procedure-related complication rates, target-limb revascularization rates, clinical improvement (ABI and Rutherford-Becker classification changes). Clinical follow up will be performed at 1, 6 and 12 months and will include physical examination, ABI measurements, Rutherford-Becker classification. Maximum follow up period will be 2 years after the index procedure.

      2 locations

      Greece (2)
      • Patras Universityu Hospital
        recruiting
        Patras, Achaia, Greece
      • Attikon university General Hospital
        recruiting
        Athens, Attiki, Greece, 15343
      Status:
      unknown
      Type:
      Interventional
      Phase:
      Start:
      30 November, 2016
      Updated:
      07 December, 2016
      Participants:
      200
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