The effect of lidocaine infusion on pain reduction and the amount of opioid consumption after surgery

Phase 3

• Conditions: aparotomy surgery.

• Registration Number: IRCT20240619062178N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 24 June 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Patients undergoing laparotomy surgery with no sensitivity to local anesthetics
No chronic use of narcotics and painkillers
No use of steroids
Age between 18 and 85 years
Absence of pregnancy
Patients according to American Society of Anesthesiologists (ASA) class one and two
Body mass index less than 40 kg/m2
Heart rate above 50 beats per minute
The recovery time is less than 45 minutes
The interval between the P wave and the R wave in the ECG is no more than 0.2 seconds

Exclusion Criteria

Patients who experience a severe drop in blood pressure, severe bradycardia (heart rate less than 40 beats per minute), moderate arterial pressure drop (mean blood pressure less than 60 mm Hg), arrhythmia, or urticaria during surgery following intravenous administration of lidocaine.
Patients whose surgery lasts more than 4 hours.

Study & Design

• Study Type: interventional
• Study Design: Not specified