跳至主要内容
临床试验/CTRI/2012/11/003099
CTRI/2012/11/003099已完成3 期

The ED50 of sevoflurane for ProSealTM and classic laryngeal mask airway placement in unpremedicated adults

Post Graduate Institute of Medical Education and Research0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Female patients of ASA status 1â??2 and aged 18-60 years, undergoing intracavity implant of caesium for cervical carcinoma under general anaesthesia

排除标准

  • Body mass index greater than 35 kg/m2, cervical spine disease, a known difficult airway, mouth opening less than 2.5 cm, upper respiratory tract symptoms in the previous 10 days, or if the patient considered at risk of aspiration (nonfasted, gastrosophageal reflux disease).

研究者

发起方
Post Graduate Institute of Medical Education and Research

相似试验

Sevoflurane anesthetic requirement for ProSeal and... | 临床试验