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
| Type | Name | Description |
|---|---|---|
| DRUG | intravenous lidocaine infusion | Lidocaine 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. |
| DRUG | Saline | Same 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.