CTRI/2025/06/089333尚未招募2 期
Comparative study between lignocaine nebulization with and without dexmedetomidine in patients undergoing awake fiberoptic intubation following airway block : a randomized controlled trial.
Department of Anaesthesiology1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年7月10日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- Intubation time after adding dexmedetomidine with lignocaine nebulization as additive to airway block during awake fiberoptic intubation
研究概览
简要总结
This study is a randomized , double-blinded trial comparing lignocaine nebulization with and without dexmedetomidine in patients undergoing awake fiberoptic intubation in IPGME&R ,Kolkata.The primary outcome measures intubation time .Secondary outcomes measures cough severity score, Intubating condition, Patient comfort score, Hemodynamic changes and complications if any.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)(—)
- 性别
- All
入选标准
- •Patients that have given written, informed consent to participate the study, American Society of Anaesthesiologist physical status 1 , patients undergoing surgery under general anaesthesia.
排除标准
- •Refusal to participate study, Allergy to local anaesthetics or any of the study drugs, pregnant and lactation, contraindication to regional nerve block like bleeding disorder and infection at the site of block, emergency operation.
结局指标
主要结局
Intubation time after adding dexmedetomidine with lignocaine nebulization as additive to airway block during awake fiberoptic intubation
时间窗: At the time from passing the fiberoptic endoscope tip through the nostril to the first reading obtained by the capnograph after endotracheal intubation
次要结局
- Cough severity score, Intubating condition, Patient comfort score, Hemodynamic changes and Complications if any(16 months)
研究者
Anwesha Mandal
IPGMER and SSKM Hospital
研究点 (1)
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