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临床试验/CTRI/2026/02/103812
CTRI/2026/02/103812招募中不适用

Efficacy of USG guided hyomental distance measurement vs classical weight based method for pLMA size selection in adult patients undergoing elective surgery : A randomized prospective study

Department Of Anaesthesia1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年2月23日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1

研究概览

简要总结

This Randomised Clinical trial aims to compare USG guided hyomental distance measurement with the conventional weight based method for selecting size of pLMA.Eligible patients will be randomised in two groups.The primary outcome will be successful device placement, and airway seal, while secondary outcomes will include ease of insertion, number of attempts and airway related complications. The study seeks to assess whether USG guided measurement offers an advantage over the traditional weight  based approach.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Double

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Age between 18 to 70 years old.
  • Either sex American Society of Anesthesiologists (ASA) physical status I – II Patients undergoing elective surgery under general anesthesia.

排除标准

  • Patiens with Refusal to participate.
  • Weight less than 30kg or more than 75kg, pregnant women..
  • High risk of regurgitation or aspiration (large hiatal hernia, history of gastroesophageal reflux disease (GERD), or uncontrolled diabetes mellitus).
  • Abnormal pharynx or anatomy Anticipated difficult airway Limited neck mobility Coagulation disorder.

研究者

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

Dr Vineet kumar

Pt BD Sharma PGIMS Rohtak

研究点 (1)

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