跳至主要内容
临床试验/CTRI/2024/04/065626
CTRI/2024/04/065626尚未招募Phase 3 4

Comparative study of intravenous bolus doses of nalbuphine with fentanyl in attenuating hemodynamic response to laryngoscopy in patients undergoing nasal intubation for oral and maxillofacial surgery (OMFS) under general anesthesia

未提供1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年5月19日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
入组人数
200
试验地点
1
主要终点
Compare the efficacy between nalbuphine and fentanyl in attenuating hemodynamic response to laryngoscopy and nasal intubation.

研究概览

简要总结

General Anesthesia administration involves laryngoscopy and endotrachial intubation which are associated with the pressor response and can lead to tachycardia, hypertension and arrhythmias, which can be deleterious in both healthy and compromised patients and hence response needs to be suppressed.Nasal intubation is the commonest endotracheal intubation method practiced during general anaesthesia in oral and maxillofacial surgeries. This study is designed to compare the efficacy of nalbuphine and fentanyl in attenuation of haemodynamic response in patients undergoing nasal intubation under general anaesthesia.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Double Blind Double Dummy

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Undergoing nasal intubation in oral and maxillofacial surgery.
  • Patient belonging to American society of Anaesthesiologist physical 1 and 2.

排除标准

  • Age>60 or <18 Preoperative hypertension, coronary artery disease (CAD), cardiac conduction defects, congenial heart disease, hemodynamic instability and associated comorbidity.
  • Obesity ( body mass index >30 kg per square meter).
  • Mouth opening less than or equal to 2.5 fingers or inability to do laryngoscopy.
  • MPG grade
  • Patients with nasal fracture.

结局指标

主要结局

Compare the efficacy between nalbuphine and fentanyl in attenuating hemodynamic response to laryngoscopy and nasal intubation.

时间窗: Intraoperatively

次要结局

  • Compare Post operative sedation(Compare post operative pain.)

研究者

发起方
未提供

研究点 (1)

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