跳至主要内容
临床试验/CTRI/2023/09/057684
CTRI/2023/09/057684尚未招募不适用

A prospective randomized comparative study to assess the safety and efficacy of Ambu Aura Gain versus I-Gel in adult patients under General Anaesthesia

Department of Anaesthesia MMCRI Mysore1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年9月24日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Oropharyngeal leak pressure

研究概览

简要总结

This study is a prospective randomised comparative study to assess the safety and efficacy of Ambu Aura gain versus I-gel in adult patients under general anaesthesia in eleective surgeries in KR hospital, Mysore, India.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • All ASA grade I and II patients between 18-50 years of both sex.
  • Elective surgeries under general anaesthesia with controlled ventilation.
  • Body mass index 25-28 Kg/m
  • Duration of surgery <2hrs.

排除标准

  • Age <18 years and > 50 years.
  • All ASA grade III and above.
  • Mallampatti grade 3 and above.
  • Emergency surgeries.
  • Head and neck surgeries.
  • Patients with decreaesed mouth opening.
  • Patients with increased risk of aspiration.
  • Patients with BMI >28 Kg/m
  • Patients with abnormal or distorted anatomy of pharynx.

结局指标

主要结局

Oropharyngeal leak pressure

时间窗: 10 min | 2 min

Time taken for insertion.

时间窗: 10 min | 2 min

Ease of Insertion &amp; number of attempts.

时间窗: 10 min | 2 min

Ease of insertion of Ryles tube .

时间窗: 10 min | 2 min

Fibreoptic bronchoscopic grading.

时间窗: 10 min | 2 min

次要结局

  • Haemodynamic response, SpO2, EtCO2(Incidence of post operative complications)

研究者

发起方
Department of Anaesthesia MMCRI Mysore
申办方类型
Government medical college

研究点 (1)

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