NCT00402870已完成不适用
Postoperative Analgesic Requirements for the ProSeal Laryngeal Mask Airway Versus the Tracheal Tube in Females Undergoing Gynecological Laparoscopic Surgery
Medical University Innsbruck2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2007年8月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 100
- 试验地点
- 2
- 主要终点
- Postoperative analgesia
研究概览
简要总结
The ProSeal laryngeal mask airway is a relatively new airway device with a modified cuff to increase the seal and a drain tube to provide a channel for regurgitated fluid, prevention of gastric insufflation and insertion of a gastric tube. In the following randomized prospective double-blind trial, we test the hypothesis that the postoperative analgesic requirements is higher for the ProSeal laryngeal mask airway than the tracheal tube.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Age 18-75
- •Elective laparoscopic surgery
排除标准
- •Known or predicted difficult airway
- •Oropharyngeal pathology
- •Mouth opening < 3.0 cm
- •A body mass index > 35 kg m-2
- •Increased risk of aspiration
- •Inability to communicate or understand the visual analogue scale
- •Analgesics within 24 hours of surgery
结局指标
主要结局
Postoperative analgesia
时间窗: 24 hrs
次要结局
未报告次要终点
研究者
研究点 (2)
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