EUCTR2010-018303-28-FR进行中（未招募）不适用
Etude pilote des signes électro-encéphalographiques de réveil secondaire à l’injection de sugammadex : évaluation par l’enregistrement de l’Index Bispectral et du NeuroSENSE (étude prospective, randomisée, monocentrique et réalisée en double aveugle) - Suggamadex-Réveil
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- Hopital Foch
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
- •Patients scheduled for general anesthesia
- •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
- •- Age under 18 years
- •- Pregnancy, non menopausal woman
- •- Allergy to propofol, soybeans or peanuts
- •- Allergy to sufentanil, remifentanil, morphine, or to a component
- •- Hypersensibility to sufentanil, remifentanil or to a derivate of fentanyl
- •- Allergy to rocuronium or to bromure ion
- •- History of a central neurological disorder or of a lesion cerebral
- •- Patients receiving a psychotropic treatment
- •- Presence of a pace-maker
- •- Hypersensibility to sugammadex or to a component
- •- Preoperative or immediate postoperative treatment with toremifene, flucloxacilline, or fusidic acid
研究者
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