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临床试验/EUCTR2007-002931-95-BE
EUCTR2007-002931-95-BE进行中(未招募)1 期

The Effects of Nitric Oxide for Inhalation on Myocardial Infarction Size. - NOMI

Z Leuven0 个研究点目标入组 230 人开始时间: 2007年11月8日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
230

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

  • The patient must meet the following criteria:
  • 1. Acute myocardial infarction (defined as an episode of chest pain or related symptom lasting greater than 2 hours but less than 12 hours and electrocardiographic evidence of ST elevation (measured as 0.08 seconds after the J point; sum >= 0.6 mV in leads I, II, III, AVL, AVF, V1-V6).
  • 2. No evidence of congestive heart failure (no S3 or evidence of pulmonary edema) and normal oxygen saturation on = 2L oxygen by NC.
  • 3. Age > 18 years.
  • 4. Signed EC approved informed consent.
  • 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 92
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 138

排除标准

  • The patient will be excluded from enrollment if any of the following are true:
  • 1. Prior myocardial infarction (as determined by patient history and/or ECG), cardiac surgery, or severe pericardial, congenital, cardiomyopathic or valvular heart disease.
  • 2. Requirement for urgent cardiac surgery.
  • 3. Previous CABG or PCI.
  • 4. Left bundle branch block.
  • 5. Unable to tolerate magnetic resonance imaging (including disallowed metallic implants or BMI > 35) or unable to tolerate gadolinium contrast media, including patients with calculated creatinine clearance less than 60 ml/min/1.73 m2 BSA.
  • 6. Active or recent hemorrhage requiring an invasive procedure for evaluation or transfusion within 6 weeks prior to presentation or hemorrhagic stroke within the 6 weeks prior to presentation.
  • 7. Known or suspected aortic dissection.
  • 8. Prior history of pulmonary disease requiring chronic oxygen therapy.
  • 9. Pregnancy, lactating and woman of childbearing potential.
  • 10. Use of investigational drugs or device within the 30 days prior to enrollment to the study. Investigational uses of approved therapies will be allowed.
  • 11. Medical problem likely to preclude completion of the study.

研究者

发起方
Z Leuven

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