Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06138041

Intravenous Lidocaine Infusion Reduce Postoperative Pulmonary Complications in Patients Undergoing Minimally Invasive Esophagectomy

Effect of Intravenous Lidocaine Infusion on Postoperative Pulmonary Complications in Patients Undergoing Minimally Invasive Esophagectomy: a Double-center, Double-blind, Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
770 (estimated)
Sponsor
Sichuan Cancer Hospital and Research Institute · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The goal of this double-center, double-blind, randomized controlled clinical trial is to compare the effect of intravenous lidocaine infusion on postoperative pulmonary complications in patients undergoing minimally invasive esophagectomy. The main question it aims to answer are whether intravenous lidocaine reduce postoperative pulmonary complications in patients undergoing minimally invasive esophagectomy. Participants will be given intravenous lidocaine infusion in lidocaine group or placebo in control group.

Conditions

Interventions

TypeNameDescription
DRUGintravenous lidocaine infusionLidocaine bolus of 2mg/kg after induction , and then continuous infusion with 2 mg/kg/h until the participate transfer out of postoperative anesthesia care unit.
DRUGSalineSame volume of normal saline in bolus and continuous infusion as lidocaine group.

Timeline

Start date
2025-02-01
Primary completion
2025-06-30
Completion
2025-08-30
First posted
2023-11-18
Last updated
2024-10-22

Source: ClinicalTrials.gov record NCT06138041. Inclusion in this directory is not an endorsement.