Comprasion of Intravenous Nalbuphine Versus Lidocaine in Reducing Propofol -Induced Injection Pain During General Surgery Procedure
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
- 是
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
Patient recieving intravenous nalbuphine prior to propofol induction
干预措施: Nalbuphine (Drug)
Lidocaine group
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
Amina Sultan
Assistant professor
Hayatabad Medical Complex