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临床试验/EUCTR2011-000157-23-NL
EUCTR2011-000157-23-NL进行中(未招募)1 期

Street Fitness In surgical patieNts undergoing general anesthesia after reversal of neuromuscular rest blockade with sugammadeX (SFINX study) - SFINX study

MC St Radboud0 个研究点目标入组 90 人开始时间: 2011年1月27日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
90

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

  • - Males and females.
  • - Age 18-65 years.
  • - Able to perform the study assessments.
  • - ASA classification 1 or 2.
  • - Medical need for general anesthesia and neuromuscular blockade.
  • - NMB with the standard dose of rocuronium. If the surgery lasts longer than 75 minutes the patient will be excluded.
  • - Minor surgical and gynecological procedures that require tracheal intubation and mechanical ventilation.
  • - Signed informed consent.
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Contra-indications for rocuronium, sugammadex, neostigmine and/or atropine.
  • - Concomitant conditions or diseases that might interfere with the study assessments.
  • - Concomitant treatment with any experimental drug within 4 weeks before surgery.

研究者

发起方
MC St Radboud

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