NL-OMON52323已完成4 期
A Prospective, Randomized, Multi-center Study to Assess the SaFety of the Orsiro Mission Stent compared to the ResoLute Onyx Stent in Subjects at High Risk for Bleeding in combination With 1-month Dual Antiplatelet Therapy (DAPT). - BIOFLOW-DAPT study
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- BIOTRONIK AG
- 入组人数
- 1
研究概览
简要总结
Trial is onging in other countries
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- An acceptable candidate for treatment with a Drug Eluting Stent (DES)
- •- Considered at high bleeding risk
- •- >= 18 years old
排除标准
- •- previously experienced stent or scaffold thrombosis in any coronary vessel.
- •- Revascularization of any target vessel within 9 months prior to the index
- •procedure or previous PCI of any non-target vessel within 72 hours prior to or
- •during the index procedure.
- •- judged by physician as inappropriate for discontinuation from DAPT at 1 month
- •following index procedure, due to another condition requiring chronic DAPT.
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