跳至主要内容
临床试验/NL-OMON30431
NL-OMON30431已完成2 期

Protect: Clinical evaluation of pacing during the onset of revascularization. Clinical feasibility study - Protect

Guidant Europe n.v. a Boston0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
50

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

  • patients presenting with their first clinically documented MI in whom the clinical decision was made to treat with PCI
  • patients older than 17 years
  • patients in whom the time from symptom onset to hospital admission is minimal 1 hour - maximal 6 hours
  • patients willing and capable of providing informed consent

排除标准

  • patients receiving thrombolytics upon clinical presentation
  • patients having previous unstable angina or ACS
  • patients having a previous PCI and/or CABG
  • clinically and hemodynamically unstable requiring circulatory support
  • Patients with a history of VF
  • Patients with a heartrate above 120 bpm at the time of enrollment

研究者

发起方
Guidant Europe n.v. a Boston

相似试验