ACTRN12611000930987已完成4 期
A single blinded, randomised controlled trial in women undergoing intermediate-duration gynaecological laparoscopy comparing the ProSeal (TM) laryngeal mask airway and the endotracheal tube.
Dr James Griffiths0 个研究点目标入组 120 人开始时间: 2011年8月30日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 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
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Adult female patients undergoing relaxant general anaesthesia for intermediate-duration gynaecological laparoscopy
排除标准
- •Anticipated surgical duration less than 30 minutes or greater than 120 minutes
- •Contraindications to the use of a LMA in laparoscopic surgery - obesity, symptoms of gastroesophageal reflux, known or anticipated difficult airway
- •Contraindications to any study drug (including morphine and parecoxib)
研究者
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