跳至主要内容
临床试验/EUCTR2008-001037-98-IT
EUCTR2008-001037-98-IT进行中(未招募)不适用

The minimum effect-site concentration of propofol that is able to prevent the responses to stimuli used to evoke cranial reflexes - ND

POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI0 个研究点开始时间: 2008年6月12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

  • - age 18 years and older
  • - general anaesthesia for elective surgery
  • - ASA (American Society of Anaesthesiologists) I-II,
  • - BMI (Body Mass Index)< 30 Kg/m2,
  • - absence of airway difficulties (Mallampati III-IV) or analgesic therapy,
  • - lack of counter-indication to propofol usage
  • 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

  • - maxillo-facial surgery

研究者

发起方
POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI

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