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Not Yet RecruitingNCT07422558

Intravenous Nalbuphine Versus Lidocaine for Prevention of Propofol Injection Pain

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

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
92 (estimated)
Sponsor
Hayatabad Medical Complex · Other Government
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

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.

Detailed description

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

Conditions

Interventions

TypeNameDescription
DRUGNalbuphineIntravenous nalbuphine 0.1mg/kg administred 60second prior to induction with propofol
DRUGLidocaineIntravenous lidocaine 4.5mg/kg (maximum 300mg) administred 60sec prior to induction with propofol

Timeline

Start date
2026-03-01
Primary completion
2026-08-01
Completion
2026-08-01
First posted
2026-02-20
Last updated
2026-02-20

Source: ClinicalTrials.gov record NCT07422558. Inclusion in this directory is not an endorsement.