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Comparative Efficacy of Propofol Lidocaine Mixture alone with Fentanyl Pretreatment and Ondansetron Pretreatment for Propofol Lidocaine Mixture to Reduce Propofol induced Pain On Injection: A Double-Blinded Randomized Controlled Trial

Phase 4
Recruiting
Conditions
Patients undergoing general anesthesia.
Lidocaine, Fentanyl, Propofol, Ondansetron, Injection pain
Registration Number
TCTR20230222006
Lead Sponsor
eurological Institute of Thailand
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
111
Inclusion Criteria

1. Age 18 - 65 years
2. Undergoing general anesthesia
3. Elective surgery
4. ASA physical status I or II

Exclusion Criteria

1. History of chronic pain
2. The patient has a history of allergy to propofol, eggs, lidocaine, fentanyl, or ondansetron.
3. Patients with liver disease
4. Patient has communication problems
5. The patient received anxiolytics or painkillers on the morning of the surgery.
6. Body mass index
greater than or equal to 30 kilograms per square meter
7. Rapid sequence intubation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Verbal Numerical Rating Scale and Behavior pain scale are recorded immediately after the propofol injection immediately after the propofol injection Verbal Numerical Rating Scale and Behavior pain scale
Secondary Outcome Measures
NameTimeMethod
incidence of adverse events; hypotension, bradycardia, and sedation. at 3 minutes after normal saline, fentanyl, ondansetron injection and 1 minute after propofol lidocaine mixture injection Patient reported outcome using a question. Clinical signs and hemodynamic changes were observed.
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