跳至主要内容
临床试验/EUCTR2013-001965-17-HU
EUCTR2013-001965-17-HU进行中(未招募)不适用

Incidence of postoperative residual neuromuscular blockade following the administration of rocuronium: A randomized placebo controlled study.

Debreceni Egyetem Orvos- és Egészségtudományi Centrum Aneszteziológiai és Intenzív Terápiás Tanszék0 个研究点开始时间: 2013年8月6日最近更新:
适应症
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

  • signed written informed consent sheet
  • - age 18-65 years
  • - ASA I-III (American Society of Anesthesiologists physical score)
  • - BMI 18,5-25 (normal body weight)
  • - expected opration time at least 50 minutes
  • - operation requiring intratracheal intubation
  • - patient in supine position and one arm is accessible
  • 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 90
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - diseases affecting neuromuscular transmission (myasthenia, myopathy, stroke, severe hepatic or renal insufficiency)
  • - medications affecting neuromuscular transmission (aminoglycoside antibiotics, magnesium)
  • - difficult airway, difficult intubation expected
  • - gravidity
  • - lactation- acute surgery
  • - glaucoma
  • - patient participated in an other trial within one month

研究者

发起方
Debreceni Egyetem Orvos- és Egészségtudományi Centrum Aneszteziológiai és Intenzív Terápiás Tanszék

相似试验

Investigation on occurence of muscle weakness after... | 临床试验