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临床试验/IRCT20201024049135N1
IRCT20201024049135N1招募中3 期

Comparison of two methods of calculating the dose of propofol for induction of general anesthesia according to either Ideal Body Weight(IBW) or Fat Free Mass(FFM), in morbid obese patient: parallel double - blinded clinical trial

Iran University of Medical Sciences0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
40

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
18 years 至 59 years(—)
性别
All

入选标准

  • Obesity BMI more than 35
  • Age 18-59 years
  • ASA ll and lll
  • Undergoing for bariatric surgery

排除标准

  • Difficult airway
  • The need for awake intubation
  • Severe systemic diseases
  • Impaired renal and hepatic function
  • History of allergies to the drugs studied
  • Behavioral disorders and the use of psychiatric drugs

研究者

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