EUCTR2008-001319-39-IT进行中（未招募）不适用
PROtection of coronary Microcirculation by Iloprost:Safety and Efficacy in Percutaneous Coronary Intervention - PROMISE PCI
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 个研究点开始时间: 2008年7月8日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Inclusion Criteria
- •1.Age > 18 y
- •2.Stable angina or inducible ischemia
- •3.Acute myocardial infarction without ST elevation (NSTEMI)
- •4.Planned angioplasty on one, two or three coronary lesions
- •5.Informed Consent
- •Subgroup with coronary flow study
- •Acute myocardial infarction without ST elevation (NSTEMI)
- •Planned angioplasty on only one stenosis or on double lesion on single vessel
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Exclusion Criteria
- •1.Atrial fibrillation (cases with coronary flow study)
- •2.ST elevation acute myocardial infarction (STEMI)
- •3.Contraindications to anti-platelet therapy or IIb/IIIa inhibitors
- •4.Hypertension (> 180/100 mmHg)
- •5.Planned angioplasty on more than three coronary stenoses
- •6.Two or more of the following procedural characteristics: stenoses in coronary bifurcations, multiple stenoses, stenoses in saphenous aorto-coronary grafts
- •7.Pregnancy or fertile age
- •Subgroup with coronary flow study
- •Atrial fibrillation
- •Proximal tortuosity of the vessel
研究者
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