跳至主要内容
临床试验/NL-OMON47500
NL-OMON47500已完成4 期

Cost-effectiveness of CYP2C19 genotype guided treatment with antipaletelet drugs in patients with ST-segment-elevation myocardial infarction undergoing immediate percutaneous coronary intervention with stent implantation: optimization of treatment. - Pharmacogenetics in STEMI

Sint Antonius Ziekenhuis0 个研究点目标入组 2,475 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
2,475

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

  • 1) more than 21 years of age with symptoms of acute myocardial infarction of more than 30 minutes but less than 12 hours
  • 2) performed primary PCI with stenting for STEMI

排除标准

  • 1) unable to give informed consent or have a life expectancy of less than one year
  • 2) active malignancy with increase in bleeding risk, in the investigator*s opinion
  • 3) women who are known to be pregnant or who have given birth within the past 90 days or who are breastfeeding
  • 4) having received thrombolytic therapy within the previous 24 hours or oral anticoagulants during the previous 7 days
  • 5) severe renal function impairment needing dialysis
  • 6) confirmed or persistent severe hypertension (Systolic Blood Pressure (SBP) > 180 mmHg and/or Diastolic Blood Pressure (DBP) >110 mmHg) at randomization
  • 7) contraindication to anticoagulation or at increased bleeding risk, at the investigator*s opinion
  • 8) cardiogenic shock (SBP <= 80mmHg for >30 mins) or needing Intra-Aortic Balloon Pump (IABP)
  • 9) history of major surgery, severe trauma, fracture or organ biopsy within 90 days prior to randomisation
  • 10) clinically significant out of range values for platelet count or haemoglobin at screening, in the investigator*s opinion.

研究者

相似试验