NL-OMON29915已完成不适用
A Clinical Evaluation of the XIENCE TM V Everolimus Eluting Coronary Stent System in the Treatment of Patients with de novo Coronary Artery Lesions - SPIRIT V
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Abbott
- 入组人数
- 225
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Maximum of one, de novo, target lesion per native major epicardial vessel or side branch (no prior stent implant, no prior brachytherapy
- •Target vessel reference diameter must be between 2.5 mm and 4.0 mm by visual estimate
- •Target lesion <28 mm in length by visual estimation
- •Target lesion must be in a major artery or branch with a visually estimated stenosis of >50% and <100% and a TIMI flow>1
- •Spirit V Registry: According tot he instructions for Use (IFU)
排除标准
- •Patient has had a known diagnosis of acute myocardial infarction within 72 hours preceding the index procedure
- •Patient has current unstable arrhythmias
- •Patient has a known left ventricular ejection fraction <30%
- •Spirit V Registry: According to the instructions for Use (IFU)
研究者
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