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临床试验/KCT0000334
KCT0000334招募中未知

Incidence of postoperative pharyngolaryngeal adverse events with LMA Supreme at high and low intracuff pressures

Konkuk University0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
o Limit 至 o Limit(—)
性别
All

入选标准

  • Patients undergoing laparoscopic surgical procedures were enrolled and written informed consent was obtained.

排除标准

  • Patients were excluded if the following criteria present: 1)known or predicted difficult airway, 2)vocal cord paralysis, 3)recent history of respiratory infection (within 1 month), 4)neurological deficits or psychiatric disorders, 5)history of drug abuse, 6)receiving current medications, 7)allergy to egg or soybean oil, 8)contraindications for use of LMA.

研究者

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