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临床试验/EUCTR2009-012815-16-DE
EUCTR2009-012815-16-DE进行中(未招募)1 期

Dosis-Wirkungsstudie von Rocuronium unter Propofol-Anästhesie (Rocuronium Dose Finding Study after single shot or steady state propofol anesthesia) - ROSANNA

Technische Universität München0 个研究点目标入组 0 人开始时间: 2009年9月24日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)

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

  • 1. ASA i to III
  • 2. patients older than 18 years
  • 3. patients where general anesthesia is planned
  • 4. patients which signed confirmed consent for this study
  • 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

  • 1. disagreement of the patient
  • 2. known or assumed allergy against anesthetics, muscle relaxans or other medication used for general anesthesia
  • 3. pregnant females or breast feeding females
  • 4. known or assumed neurmuscular disease
  • 5. burn injury
  • 6. anatomic or functional malformation where dfficult intubation is expected
  • 7. anorexia, malnutrition or bulimia
  • 8. heart failure

研究者

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