跳至主要内容
临床试验/PACTR201608001710307
PACTR201608001710307招募中未知

Safety and Efficacy of Ketamine-Dexmedetomidine versus Ketamind-Propofol Combinations for Sedation in Patients after Coronary Artery Bypass Graft Surgery

Tanta Univercity hospital anaesthesia department and Cardiothoracic surgery departement0 个研究点目标入组 60 人开始时间: 2016年7月10日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
60

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
40 Year(s) 至 60 Year(s)(—)
性别
All

入选标准

  • Patients 40-60 years old hemodynamically stable with normal or moderately impaired left ventricular function ejection fraction (EF) > 40%; who underwent elective coronary artery bypass graft surgery under high-dose opioid anesthesia on mechanical ventilation

排除标准

  • -Patient refusal.
  • -Pregnant patients.
  • -Patients with neurologic disease
  • -Patients with liver or renal insufficiency
  • -Hemodynamic instability both intraoperative, post bypass or postoperative
  • -Patients on high dose vasopressor or inotropes.
  • -Patients need muscle relaxant.
  • -Patients need postoperative mechanical ventilation more than 24 hours.

研究者

发起方
Tanta Univercity hospital anaesthesia department and Cardiothoracic surgery departement

相似试验