JPRN-UMIN000012104已完成未知
Japan study of Distal Evaluation of Functional significance of Intra-arterial stenosis Narrowing Effect. - Japan study of Distal Evaluation of Functional significance of Intra-arterial stenosis Narrowing Effect.
PO Associations for Establishment of Evidence in Interventions0 个研究点目标入组 500 人开始时间: 2013年10月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 500
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
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. Patient with known contraindications to ATP and/or papaverine hydrochloride 2. Target vessel diameter<=2.0mm 3. Lesion with CTO (registration allowed if other branch has stenosis more than 50% in visual judgment) 4. Patient with temporary/permanent artificial pacemaker implantation, left bundle branch block, second-degree and third-degree atrioventricular block. 5. AMI patient 6. Patient who is disqualified for FFR and coronary revascularization by the investigator. 7. Lesion is disqualified for PCI by the investigator. 8. Patient who has critical valvular disease of heart. (moderate or severe AS/AR/MS/MR) 9. Patient with a prior CABG on target vessel. 10. Patient with severe renal dysfunction. (serum creatinine>=2.0mg/dl) 11. Patient on hemodialysis. 12. Body weight>=200kg 13. Patient who needs ventricular assist device to ensure hemodynamic stability (heart rate<50/min, SBP<90mmHg) 14. Patient who expects to live less than 2 years at the registration 15. Patient with contraindications to an antithrombotic therapy or an anticoagulant therapy. 16. Patient who is poor compliance with drug treatment. 17. Patient who is allergic to contrast agent. 18. LVEF>=30% 19. Patient who has the history of PCI with DES in recent 3 months before registration. 20. Patient who has the history of PCI with BMS or POBA in recent 1 year before registration. 21. Patient who has possibility of pregnancy, under breast-feeding and positive pregnancy test in 14days prior to the PCI. 22. Patients with inadequacy to join this clinical study. 23. Patient who has been enrolled any other clinical study.
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