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临床试验/ISRCTN72444640
ISRCTN72444640已完成未知

Evaluation of late clinical events after drug-eluting versus bare-metal stents in patients at risk: BAsel Stent Kosten Effektivitäts Trial - PROspective Validation Examination

niversity Hospital Basel (Switzerland)0 个研究点目标入组 2,400 人开始时间: 2007年2月1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
2,400

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

性别
All

入选标准

  • 1. All comers, 24 hours a day, seven days a week, irrespective of indication for Percutaneous Coronary Intervention (PCI)
  • 2. With the need for large (more than or equal to 3.0 mm stents only) native vessel stenting

排除标准

  • 1. In-stent-restenosis
  • 2. Bypass graft disease
  • 3. Main stem disease to be stented
  • 4. Cardiogenic shock
  • 5. Planned surgery within the next six months
  • 6. Oral anticoagulation needed (artificial heart valves, atrial fibrillation)
  • 7. No compliance expected
  • 8. Enrolled in another study
  • 9. No consent

研究者

发起方
niversity Hospital Basel (Switzerland)

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