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RECRUITING
NCT06923787
PHASE2

Effect of Perioperative Intravenous Infusion of Lidocaine on the Postoperative Course and the Immune Response in Patients Undergoing Surgery for Colon Cancer - the PILDI Study

Sponsor: Institute of Oncology Ljubljana

View on ClinicalTrials.gov

Summary

There are very few data in the literature on changes in inflammatory markers when lidocaine is administered perioperatively in patients with colorectal cancer. In patients undergoing surgery for colon cancer, the aim is to conduct a double-blind placebo-controlled study to determine differences in levels of pro-inflammatory markers, postoperative pain and opioid analgesic consumption in the first two days after surgery, and the time to first postoperative bowel movement. Groups of patients receiving perioperative lidocaine infusion, high dose dexamethasone or placebo will be compared.

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-02-03

Completion Date

2028-07-01

Last Updated

2026-02-05

Healthy Volunteers

No

Conditions

Interventions

DRUG

Lidocaine

intravenous infusion of lidocaine

DRUG

Placebo

saline solution intravenous infusion

Locations (2)

Institute of Oncology Ljubljana

Ljubljana, Slovenia

Institute of Oncology Ljubljana

Ljubljana, Slovenia