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临床试验/CTRI/2025/09/094814
CTRI/2025/09/094814已完成Unknown

A Cross Sectional Study Comparing the Effects of Sevoflurane and Desflurane in adults patients undergoing General Anesthesia with Laryngeal Mask Airway

Department of Anesthesiology1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年9月15日最近更新:

试验速览

阶段
Unknown
状态
已完成
入组人数
60
试验地点
1
主要终点
To observe and compare group A and B regarding the total volume of the inhalational agent, namely Sevoflurane or Desflurane used, total dose of the analgesic drug requirement, intraoperative hemodynamic stability, oxygen saturation, postoperative recovery score, and postoperative side effects, if any, will be assessed and documented for comparison

研究概览

简要总结

This research aims to evaluate and compare the clinical performance of two inhalational anaesthetic agents—sevoflurane and desflurane, in adult patients scheduled for elective surgical procedures under general anaesthesia (GA) using a laryngeal mask airway (LMA). The study will assess key perioperative parameters, including the duration of surgery, intraoperative Oxygen saturation, Haemodynamic stability based on heart rate, blood pressure, mean arterial pressure and postoperative recovery characteristics based on recovery score and side effects such as nausea, vomiting and delirium.

The goal is to determine which agent offers superior outcomes in terms of anaesthetic efficiency, patient safety, and recovery quality.

研究设计

研究类型
Observational

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 physical status I and II Patients scheduled for elective surgery under GA with LMA Patient is willing to participate in the research.

排除标准

  • ASA physical status III and above Pregnant patients, paediatric patients Patient scheduled for emergency surgeries Patient with a history of smoking, chronic alcoholism, drug abuse, and psychiatric disorder Patient refusal.

结局指标

主要结局

To observe and compare group A and B regarding the total volume of the inhalational agent, namely Sevoflurane or Desflurane used, total dose of the analgesic drug requirement, intraoperative hemodynamic stability, oxygen saturation, postoperative recovery score, and postoperative side effects, if any, will be assessed and documented for comparison

时间窗: Before starting the procedure, the baseline parameters of vital signs, SpO2, Heart rate, blood pressure, ECG, and temperature will be assessed. After every 10 minutes till the end of the surgery duration of surgery post post-operative recovery score, and once the patient recovers from General anaesthesia, all these parameters will be assessed and compared between the two groups

次要结局

  • Nausea, Vomiting, Sore throat(Hourly for 4hrs then after 24hrs)

研究者

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

Ms A Jayaprabha

BIHER university

研究点 (1)

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