Multi-center, Randomized Trial Comparing Dual Antiplatelet Therapy With CILOstazol Plus Aspirin Versus Aspirin Alone Following PERipheral Endovascular Procedures
试验速览
- 阶段
- 3 期
- 发起方
- 入组人数
- 200
- 试验地点
- 2
- 主要终点
- Composite endpoint of major adverse cardiovascular and limb events
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 85 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- •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
研究组 & 干预措施
Group Cilostazol
Patients receiving dual antiplatelet therapy with cilostazol 100mg twice daily and aspirin 100mg once daily for 12 months.
干预措施: Cilostazol (Drug)
Group Cilostazol
Patients receiving dual antiplatelet therapy with cilostazol 100mg twice daily and aspirin 100mg once daily for 12 months.
干预措施: Aspirin (Drug)
Group Aspirin
Patients receiving monotherapy with aspirin 100mg once daily for 12 months.
干预措施: Aspirin (Drug)
结局指标
主要结局
Composite endpoint of major adverse cardiovascular and limb events
时间窗: 1 year
次要结局
- Ankle-Brachial Index (ABI) changes(6 and 12 months)
- Clinical improvement(1-year)
- Quality of life assessment(1 year)
- Drug-related complications(1 year)
- Procedure-related complications(1 month)
- Blood cholesterol level monitoring(6 and 12 months)
- Blood glucose level monitoring(6-12 months)
研究者
Stavros Spiliopoulos
Assistant Professor of Radiology
Attikon Hospital
