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临床试验/JPRN-UMIN000034936
JPRN-UMIN000034936已完成未知

Onyx ONE Clear Study: A Single Arm Study with Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk Patients who are considered One-Month Clear - Onyx ONE Clear Study: A Single Arm Study with Resolute Onyx in ONE-Month DAPT for High-Bleeding Risk Patients who are considered One-Month Clear

Medtronic Japan Co., Ltd0 个研究点目标入组 800 人开始时间: 2018年11月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
800

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Pregnant and breastfeeding women 2) Subjects requiring a planned PCI procedure after one month of index procedure 3) Procedure planned to require non-study stents, stand-alone POBA, or stand-alone atherectomy 4) Active bleeding at the time of inclusion 5) Cardiogenic shock 6) Subject with planned surgery or procedure necessitating discontinuation of DAPT within one month following index procedure 7) Subject not expected to comply with long-term single antiplatelet therapy 8) A known hypersensitivity or contraindication to aspirin, heparin and bivalirudin, P2Y12 inhibitors, mTOR inhibiting drugs such as zotarolimus, cobalt, nickel, platinum, iridium, chromium, molybdenum, polymer coatings (e.g., BioLinx), stainless steel (or other metal ions found in 316L stainless steel), zinc, or a sensitivity to contrast media, which cannot be adequately pre-medicated. 9) PCI during the previous 6 months for a lesion other than the target lesion of the index procedure 10) Participation in another clinical study within 12 months after index procedure 11) Subjects with life expectancy of less than 2 years

研究者

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