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
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.
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