Skip to content

Intravenous Lidocaine for Laparoscopic Cholecystectomy

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01062906
Enrollment
80
Registered
2010-02-04
Start date
2010-03-31
Completion date
2010-03-31
Last updated
2011-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Consumption, Postoperative Pain

Keywords

intravenous lidocaine, postoperative pain, laparoscopic surgery, opioids, opioids side-effects

Brief 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.

Interventions

DRUGLidocaine

1.5 mg/Kg as bolus and a continuous infusion of 2mg/Kg/hr until the end of surgery (closure of the skin)

DRUGFentanyl

Fentanyl 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)

Sponsors

McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* patients undergoing laparoscopic cholecystectomy

Exclusion criteria

* age \<18 yr or \> 85 yr, * ASA physical status 3 and greater, history of hepatic failure (Child & Pug A-C), * renal failure (creatinine outside the normal range) or cardiac failure (NYHA I-IV), * Adams-Stoke syndrome, * severe degrees of sinoatrial, atrioventricular or intraventricular block, * organ transplant, * diabetes mellitus type 1 and 2, * morbid obesity (BMI \> 40), * chronic use of opioids and beta-blockers, * known seizures, * severe mental impairment, * allergy to local anesthetics and to all the medications used in the study, or * inability to understand pain assessment.

Design outcomes

Primary

MeasureTime frame
Fentanyl consumption (measured as fentanyl equivalents -mcg)postoperative day 0 (day of surgery before beeing discharged home) and 24 hr after the end of surgery

Secondary

MeasureTime frame
Pain, Static and DynamicOn postoperative day 0 (day of surgey before beeing discharged home) and 24 hrs after the end of surgery
Opioids side-effectsOn postoperative day 0 (before beeing discharged home) and at 24 hrs after the end of surgery

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026