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.
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