Clinical Trials Directory

Trials / Completed

CompletedNCT03677817

Perioperative Lidocaine Administration in Thoracoscopic Surgery for Improved Postoperative Pain Control

Prospective, Randomized, Double Blind, Superiority Trial, Evaluating the Effect of Perioperative Lidocaine on Postoperative Opioid Consumption, Pain Ratings, Duration of Hospital Stay, Time to First Defecation, 30-day Mortality and Development of Chronic Pain in Patients Undergoing Video-assisted Thoracoscopic Procedures

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
113 (actual)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Placebo-controlled study to analyze the effect of perioperative intravenous lidocaine administration on total morphine consumption (TMC) and on pain intensity in thoracoscopic surgery .

Detailed description

Thoracoscopy (thoracic surgery) is a video-assisted minimally invasive operation in thoracic surgery, which is associated with pain after surgery. Trial drug Lidocaine is approved as pain medication. This placebo-controlled study analyzes the effect of perioperative intravenous lidocaine administration on total morphine consumption (TMC) and on pain intensity in thoracoscopic surgery . Half of the patients will receive NaCl 0.9% (a saline solution without active ingredient) instead of Lidocaine.

Conditions

Interventions

TypeNameDescription
DRUGLidocaineregimen of lidocaine administration of 1,5 mg/kg, IV bolus, followed by continuous infusion at 3,0 mg/kg/h
DRUGNaCl 0,9%IV bolus of NaCl 0,9%, followed by continuous infusion of NaCl 0,9%

Timeline

Start date
2019-04-03
Primary completion
2022-08-28
Completion
2022-08-28
First posted
2018-09-19
Last updated
2022-09-07

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT03677817. Inclusion in this directory is not an endorsement.