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临床试验/EUCTR2012-001495-11-CZ
EUCTR2012-001495-11-CZ进行中(未招募)1 期

The effect of intracoronary reinfusion of bone marrow-derived mononuclear cells (BMMNC) on all causemortality in acute myocardial infarction - BAMI

Queen Mary University London0 个研究点目标入组 375 人开始时间: 2014年3月17日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
375

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Signed and dated informed consent
  • 2. Men and women of any ethnic origin aged = 18 years
  • 3. Patients with acute STelevation (including new LBBB)
  • myocardial infarction as defined by the universal definition of AMI.
  • 4. Successful acute reperfusion therapy (residual stenosis visually <50% and TIMI flow =2) within 24 hours of symptom
  • onset or thrombolysis within 12 hours of symptom onset followed by successful percutaneous coronary intervention
  • (PCI) within 24 hours after thrombolysis
  • 5. Left ventricular ejection fraction = 45% with significant regional wall motion abnormality assessed by quantitative
  • echocardiography (central, independent core lab analysis) 3 to 6 days after reperfusion therapy
  • 6. Open coronary artery suitable for cell infusion supplying the target area of abnormal wall motion
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 1800
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 1200

排除标准

  • 1. Participation in another clinical trial within 30 days prior to randomisation
  • 2. Previously received stem/progenitor cell therapy
  • 3. Pregnant or nursing women
  • 4. Mental condition rendering the patient unable to understand the nature, scope and possible consequences of the
  • study or to follow the protocol
  • 5. Necessity to revascularise additional vessels, outside the target coronary artery at the time of BMMNC
  • (additional revascularisations after primary PCI and before BMMNC
  • cell infusion are allowed), unless clinically indicated and according to latest guidelines. this decision should be made at the time of the index procedure and explicitly stated at the time
  • 6. Cardiogenic shock requiring mechanical support
  • 7. Platelet count <100,000/µl, or hemoglobin <8.5 g/dl
  • 8. Impaired renal function, i.e. serum creatinine >2.5 mg/dl
  • 9. Persistent fever or diarrhea not responsive to treatment within 4 weeks prior screening
  • 10. Clinically significant bleeding within 3 months prior screening
  • 11. Uncontrolled hypertension (systolic >180 mmHg and diastolic >120 mmHg)
  • 12. Life expectancy of less than 2 years from any noncardiac
  • cause or neoplastic disease

研究者

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