Comparative evaluation of i-gel insertion conditions using dexmedetomidine versus fentanyl - A randomised controlled study
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- To assess ease of I gel insertion using youngs criteria, lund and stoyener grading
研究概览
简要总结
The study is to compare the conditions under which an i-gel® (a type of supraglottic airway device) is inserted when patients are administered dexmedetomidine versus fentanyl. This randomized controlled trial aims to determine which sedative agent provides better insertion conditions.
Dexmedetomidine, known for its sedative and analgesic properties, is compared to fentanyl, a potent opioid analgesic. The primary focus is on the ease of i-gel® insertion, as well as any differences in patient outcomes, such as comfort and hemodynamic stability. The results of the study would help in choosing the most effective sedative agent to improve the success and safety of i-gel® insertion in clinical settings.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients posted for elective surgeries under general anaesthesia Age: 18 -60 years.
- •ASA physical status 1 or 2.
排除标准
- •Severe respiratory or cardiac disorders, hepatic or renal insufficiency, coagulopathy.
- •Allergy to any of the study drug (Test dose to be given).
- •Pregnancy or breast feeding.
结局指标
主要结局
To assess ease of I gel insertion using youngs criteria, lund and stoyener grading
时间窗: to assess ease of I gel insertion using youngs criteria, lund and stoyener grading
次要结局
- To assess overall condition of I gel insertion using modified scheme of lund & stovner(base line haemodynamic parameter such as heart rate,blood pressure, respiratory rate. before insertion & 1,3,5and 10 minutes after insertion)
研究者
Sindhura
sri devaraj urs medical college