Clinical Trials Directory

Trials / Completed

CompletedNCT01062906

Intravenous Lidocaine for Laparoscopic Cholecystectomy

The Effect of Intravenous Lidocaine on Short-term Outcomes After Laparoscopic Cholecystectomy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Intravenous lidocaine has been shown to have analgesic, antinflammatory, antihyperalgesic, antithrombotics and neuroprotective properties. In a previous study conducted in patients undergoing laparoscopic cholecystectomy under general anesthesia with desflurane and fentanyl, intraoperative i.v. infusion of lidocaine spared opioids consumption in the recovery room by 30%. The purpose of this study was to determine if an i.v. infusion of lidocaine without intraoperative opioids would reduce the amount of fentanyl to the same extent and opioids-related side effects.

Conditions

Interventions

TypeNameDescription
DRUGLidocaine1.5 mg/Kg as bolus and a continuous infusion of 2mg/Kg/hr until the end of surgery (closure of the skin)
DRUGFentanylFentanyl 3 mcg/Kg as bolus at the induction and a continuous infusion of normal saline (NaCl 0.9%) until the end of surgery (skin closure)

Timeline

Start date
2010-03-01
Primary completion
2010-03-01
Completion
2010-03-01
First posted
2010-02-04
Last updated
2011-01-13

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01062906. Inclusion in this directory is not an endorsement.