EUCTR2012-004163-50-ES进行中（未招募）不适用
Comparative, randomized, double-blind clinical trial on end-tidal concentration of sevoflurane associated to remifentanil required for insertion of the SupremeLaryngeal Mask vs. Pro-Seal Laryngeal Mask
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
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
- •ASA I and II patients,
- •aged 18-75 years,
- •they are to be conducted outpatient surgery using laryngeal mask: minor procedures vascular surgery, abdominal, plastic, urological and minor orthopedic surgery
- •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 50
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •?background of of difficult airway
- •? difficult airway parameters, combining Mallamapati III or IV, thyromental distance <6 cm and decreased mouth opening < than 3 cm.
- •? Risk factors of aspiration of gastric contents: hiatal hernia symptoms frequent (daily or weekly)
- •? History of recent respiratory infection.
- •? Pregnancy and breastfeeding.
- •? Patient refusal to participate in the study.
研究者
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