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临床试验/NL-OMON48996
NL-OMON48996已完成4 期

MRI measurement of the effects of moderate versus deep neuromuscular blockade on the abdominal working space during laparoscopic surgery in a prospective cohort study. - RELAX-2 study

Radboud Universitair Medisch Centrum0 个研究点目标入组 10 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
10

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 至 99(—)

入选标准

  • - all adult patients (18 years or older) scheduled for laparoscopic donor nephrectomy
  • - obtained informed consent

排除标准

  • * Unable to provide informed consent
  • * known or suspect allergy to mivacurium, rocuronium or sugammadex
  • * neuromuscular disease
  • * indication for rapid sequence induction
  • * Being unable to undergo MRI due to any reason (e.g. non MRI-compatible implants, epilepsy)
  • * Deficiency of vitamin K-dependent clotting factors, coagulopathy or active use of coumarin derivates.
  • * Peri-operative use of fusidic acid or flucloxacilline
  • * Severe renal impairment (creatinine clearance <30ml/min)
  • * BMI> 30 kg/m2
  • * ASA-score > 2

研究者

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