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临床试验/NCT07422558
NCT07422558
尚未招募
不适用

Comprasion of Intravenous Nalbuphine Versus Lidocaine in Reducing Propofol -Induced Injection Pain During General Surgery Procedure

Hayatabad Medical Complex0 个研究点目标入组 92 人开始时间: 2026年3月1日最近更新:

概览

阶段
不适用
状态
尚未招募
入组人数
92
主要终点
Frequency of propofol- induced injection pain

概览

简要总结

Propofol is a commonly used intravenous anesthetic agent, but its administration is frequently associated with injection pain, causing patient discomfort and agitation. Various pharmacological agents have been used to reduce this pain, including nalbuphine and lidocaine; however, results from previous studies remain conflicting. This randomized clinical trial aims to compare the effectiveness of intravenous nalbuphine versus intravenous lidocaine in reducing the frequency of propofol-induced injection pain in patients undergoing elective general surgery procedures.

详细描述

Propofol-induced injection pain is a common and undesirable adverse effect that can lead to patient distress during induction of anesthesia. Nalbuphine, a kappa-opioid receptor agonist and partial mu-opioid receptor antagonist, and lidocaine, a sodium channel blocker, have both been used to reduce this pain, but evidence regarding their comparative effectiveness remains inconsistent.

This randomized clinical trial will be conducted in the Department of Anesthesiology, PGMI / Hayatabad Medical Complex, Peshawar. A total of 92 adult patients with ASA physical status I-II, scheduled for elective general surgery under general anesthesia, will be enrolled and randomized into two equal groups. Group A will receive intravenous nalbuphine at a dose of 0.1 mg/kg, while Group B will receive intravenous lidocaine at a dose of 4.5 mg/kg (maximum 300 mg), administered 60 seconds prior to induction with propofol. Injection pain will be assessed by the inducing anesthesiologist using a four-point pai

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-60 years
  • Either male or female
  • ASA physical status I or II
  • Scheduled for elective general surgery under general anesthesia using propofol

排除标准

  • Known hypersensitivity to propofol, nalbuphine, or lidocaine
  • Emergency surgery
  • Use of analgesics prior to surgery
  • Pregnant women
  • Lactating women

研究组 & 干预措施

Nalbupine group

Experimental

Patient recieving intravenous nalbuphine prior to propofol induction

干预措施: Nalbuphine (Drug)

Lidocaine group

Active Comparator

Patient recieving intravenous lidocaine prior to propofol induction

干预措施: Lidocaine (Drug)

结局指标

主要结局

Frequency of propofol- induced injection pain

时间窗: During induction of anesthesia (within 1-2 minutes of propofol administration

Presence of injection pain assessed using a four-point pain scale during propofol injection until loss of eyelash reflex. Pain score ≥1 will be considered as presence of injection pain.

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Amina Sultan

Assistant professor

Hayatabad Medical Complex

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