CTRI/2023/06/053992尚未招募4 期
A randomised double blinded study to compare the effectiveness of intravenous Fentanyl, intravenous Dexmeditomidine & topical Lignocaine for tolerance to Laryngeal mask airway insertion with Propofol induction.
Indira Gandhi Institute of Medical Sciences ,Patna1 个研究点 分布在 1 个国家目标入组 147 人开始时间: 2023年6月20日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 147
- 试验地点
- 1
- 主要终点
- To acheive optimal condition for Laryngeal mask airway insertion.
研究概览
简要总结
The purpose of this study is to compare the effectiveness of three drugs, intravenous Fentanyl, intravenous Dexmeditomidine and topical Lignocaine before induction with Propofol in providing better comfort during Laryngeal mask airway insertion for securing airway and ventilation in patients undergoing elective surgery under General Anaesthesia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant, Investigator and Outcome Assessor 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
- •1.Age 18 to 60 years.
- •2.Both gender.
- •3.Patients with ASA physical status 1 and
- •4.Posted for elective surgery under General Anaesthesia.
排除标准
- •1.Patients with increased risk of aspiration.
- •2.Allergy to any of the study drugs.
- •3.Basal metabolic index >30 kg/m
- •4.Patient refusal.
- •5.Difficult airway and facial anomaly.
- •6.Patient with ASA physical status III & IV.
结局指标
主要结局
To acheive optimal condition for Laryngeal mask airway insertion.
时间窗: At the time of Laryngeal mask airway insertion.
Muzi & colleagues score less than or equal to 2 will be considered as optimal.
时间窗: At the time of Laryngeal mask airway insertion.
次要结局
- To look for any side effects of study drugs.(During LMA insertion till 24 hours postoperative .)
- Airway complications like sore throat & hoarseness of voice or any change in voice.(24 hrs postoperative)
研究者
研究点 (1)
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