Overview
The aim is to analyze the effect of intravenous lidocaine administration on postoperative opioid use in patients undergoing upper abdominal cancer surgery. Specifically, those patients undergoing gastric cancer surgery and liver cancer surgery using a laparoscopic approach
Description
In a recent Cochrane Library review, despite the apparent positive results reported by intravenous administration of lidocaine as a perioperative analgesic adjuvant, the quality of the evidence is low, since the studies carried out to date present small samples, great variability in the designs and different surgical techniques studied.
More studies will be needed to help improve the grade and quality of evidence in the management of acute postoperative pain and its role in opioid sparing, an especially beneficial effect in tumor pathology For this reason, the investigators have designed a randomized, double-blind, phase IV clinical trial with two treatment arms, parallel groups, in which 96 patients who underwent liver and gastric cancer surgery through laparoscopic approach participated.
This study will include 2 different population groups: patients undergoing liver cancer surgery and patients undergoing gastric cancer surgery
Eligibility
Inclusion Criteria:
- Men and women over 18 years of age scheduled for gastric or liver cancer surgery through a laparoscopic approach at the University of Girona Dr Josep Trueta.
- Accept and sign the informed consent
Exclusion Criteria:
- decline participating in the study at any stage of its development.
- History of allergic or adverse reactions to Amide-type anesthetics.
- Pregnancy or lactation period
- Diagnosis of Child-Pugh stage B or C liver failure.
- Acute renal failure (GFR <60 ml / min).
- Concomitant treatment with opioids for chronic pain.
- Any condition that, in the clinical judgment of the researchers, may interfere with the object of the research.