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临床试验/EUCTR2010-021844-17-NL
EUCTR2010-021844-17-NL进行中(未招募)不适用

Perioperative esmolol infusion for haemodynamic stability during major vascular surgery. - Perioperative esmolol infusion

Erasmus Medical Centre0 个研究点开始时间: 2010年7月27日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • Patients are eligible for inclusion for the study at the Erasmus Medical Centre if they are:
  • 1. Scheduled for arterial vascular surgery, including abdominal aortic aneurysm repair, abdominal aortic stenosis surgery, lower limb arterial reconstruction or carotid artery stenosis repair
  • 2. Provide informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Potential subjects will be excluded with any of the following:
  • 1. Active bleeding
  • 2. Untreated left main disease
  • 3. Active cardiac condition such as unstable angina pectoris, active congestive heart failure, serious cardiac arrhythmias, symptomatic valvular disease, recent MI< 6 months.
  • 4. Preoperative positive troponin T
  • 5. Contraindication for esmolol use
  • 6. Previous allergy or intolerance to esmolol
  • 7. Cancer with an expected life expectancy < 6 months
  • 8. Excessive alcohol use
  • 9. Pregnancy or planning to become pregnant
  • 10. Failure to provide informed consent
  • 11.Failure to monitor heart rate with the continuous 12-lead electrocardiography because of surgery or baseline electrocardiographic abnormalities.

研究者

发起方
Erasmus Medical Centre

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