Comparing the Efficacy Between Lignocaine Given Via MADgic Atomizer and Lignocaine Pump Spray Pre Endotracheal Intubation in Adult Undergoing General Anesthesia.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 125
- 试验地点
- 1
- 主要终点
- Severity Grading of Post Operative Sore Throat
研究概览
简要总结
Comparing the efficacy between Lignocaine given via MADgic Atomizer and Lignocaine Pump Spray pre endotracheal intubation in adult undergoing General Anesthesia.
详细描述
Comparing the efficacy of Lignocaine given via 2 device (Lignocaine Spray and MADGIC Atomizer) on hemodinamic parameters postintubations and severity grading of post operative sore throat, cough and hoarseness of voice.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
盲法说明
Participant and Outcome Assessor do not know type of intervention
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Adult with the age of 18 to 65 years old
- •Gender of both male and female
- •Planned for elective surgery scheduled at General Operation Theatre that require elective intubation for general anesthesia
- •American Society Anaesthesiologist (ASA) preoperative physical status assessment of 1 and 2
- •Airway assessment Malampati scoring 1and 2.
排除标准
- •Pregnancy
- •Known allergy or hypersensitivity to Lignocaine
- •Pre existing sore throat or hoarseness of voice identified during preoperative assessment.
- •The use of airway device other than endotracheal tube (ETT) such Laryngeal Mask airway/Supraglottic Device'
- •Oral and neck surgery
研究组 & 干预措施
MADgic Atomizer
Group M(MADgic) acting as Intervention Group:
Patients receiving Lignocaine 30mg (3 alliquotes) given via MADgic Laryngotracheal Atomization Device prior to endotracheal intubation.
干预措施: MADgic Atomizer (Device)
Lignocaine Spray
Group S (Spray) acting as Control Group:
Patients receiving Lignocaine 30 mg (3 puffs) given via 10mg Lignocain Pump Spray prior to endotracheal intubation.
干预措施: Lignocaine pump spray (Device)
结局指标
主要结局
Severity Grading of Post Operative Sore Throat
时间窗: 24 hours
Numbers of participants complaining incidence of sore throat postoperatively
次要结局
- Severity Grading of Post Operative Cough(24 hours)
- Severity grading of Hoarseness of voice(24 hours)
研究者
Rhendra Hardy Mohamad Zaini
Asssociate Proffessor
Universiti Sains Malaysia