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临床试验/CTRI/2026/01/101397
CTRI/2026/01/101397尚未招募2/3 期

A prospective randomised study comparing the clinical performance of Proseal LMA and Baska Mask in adult patients undergoing elective surgery under general anaesthesia with controlled ventilation.

Department of Anaesthesia1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年1月21日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
80
试验地点
1
主要终点
To compare the clinical performance of both the LMA

研究概览

简要总结

This study is a prospective randomised study comparing the clinical efficacy of the Proseal LMA and Baska mask in adult patients undergoing elective surgeries in general anaesthesia with controlled ventilation.

we will be assessing number of attempts taken for successful insertion, oropharyngeal seal pressure, ease of insertion of device, hemodynamic parameters, and complications if any.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • ASA Grade 1 and 2 undergoing elective surgery in supine position under general anaesthesia.

排除标准

  • ASA Grade3/4 pregant patient surgery duration more than 4 hours.

结局指标

主要结局

To compare the clinical performance of both the LMA

时间窗: postoperatively complications to be assessed for 24 hours if any

次要结局

  • number of attempts for successful insertion of device(patients to be assessed for 24 hours postoperatively)
  • orophayngeal seal pressure(patients to be assessed for 24 hours postoperatively)
  • complications if any(patients to be assessed for 24 hours postoperatively)

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Monika

LLRM Medical College

研究点 (1)

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