跳至主要内容
临床试验/CTRI/2025/12/098715
CTRI/2025/12/098715尚未招募不适用

Comparison of intubating conditions with combination of Fentanyl-Lidocaine-Propofol versus Fentanyl-Dexmedetomidine-Propofol in absence of neuromuscular blocking agent

Dr Sripriya1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2025年12月21日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
56
试验地点
1
主要终点
Comparing intubating conditions in combination of fentanyl-dexmedetomidine-propofol with fentanyl-lidocaine-propofol in absence of neuromuscular relaxant

研究概览

简要总结

This prospective randomized comparative study aims to evaluate whether the combination of Fentanyl–Dexmedetomidine–Propofol provides superior intubating conditions compared to Fentanyl–Lidocaine–Propofol during endotracheal intubation without neuromuscular blocking agents in ASA I–II adults aged 18–60 years undergoing elective surgery under general anesthesia. A total of 56 patients will be randomized into two groups, receiving either fentanyl with lidocaine or fentanyl with dexmedetomidine prior to induction with propofol, and intubating conditions will be assessed using the Viby–Mogensen scoring system along with monitoring hemodynamic responses for 5 minutes post-intubation. The study seeks to determine which drug combination better suppresses airway reflexes, provides smoother intubation, and maintains greater hemodynamic stability, while also observing any adverse events and the need for rescue muscle relaxants. The findings aim to guide safe and effective intubation practices when neuromuscular blockers are contraindicated or undesirable.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
16.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • ASA grade I and II Patients undergoing elective surgeries under general anaesthesia Patient willing to give written informed consent.

排除标准

  • Patients with history of reactive airway disease, oesophageal reflux , previous difficulty with intubation or a suspected difficult airway.
  • Patients with allergy to any of the study drugs.
  • Patients with pre-existing cardiovascular, renal and hepatic disorders.
  • Surgical procedures which lasts more than 4 hrs will be excluded from the study.

结局指标

主要结局

Comparing intubating conditions in combination of fentanyl-dexmedetomidine-propofol with fentanyl-lidocaine-propofol in absence of neuromuscular relaxant

时间窗: Comparing intubating conditions during intubation and every 1 min for 5 minutes post intubation

次要结局

未报告次要终点

研究者

发起方
Dr Sripriya
申办方类型
Other [Self ]
责任方
Principal Investigator
主要研究者

Sripriya

Grant government medical college and JJ hospital

研究点 (1)

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