跳至主要内容
临床试验/EUCTR2005-004398-76-GB
EUCTR2005-004398-76-GB进行中(未招募)不适用

A comparison of Myocardial Protection Using Preconditioning with Sevoflurane Against High Thoracic Epidural Analgesia for CABG Surgery

Golden Jubilee National Hospital0 个研究点目标入组 150 人开始时间: 2006年2月20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)
入组人数
150

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 presenting for elective CABG operations, with >40 % left ventricular ejection fraction, aged 40-80.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients at risk of epidural haematomas (i.e. platelets <100, coagulopathies, on anticoagulant therapies, INR>1.4) or unsuited to HTEA (patient refusal, spinal deformities).
  • Patients on drugs shown to manipulate the preconditioning phenomenon will also be excluded. This includes those on diazoxide, nicorandil, oral sulfonylureas and theophyllines.
  • Patients with preoperative ECG morphologies likely to make interpretation difficult or impossible including: left bundle branch block, cardiac pacemaker dependence.
  • Haemodynamically compromised patients requiring inotropic or balloon pump support preoperatively.
  • Significant valvular disease.
  • Preoperative elevated levels of troponin I or CKMB.
  • Unstable angina or angina in 24 hours preop.

研究者

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