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NCT06272461Recruiting

Comparison of Intravenous Lidocaine vs Ketamine in Colorectal Surgery

The Effect of Intravenous Lidocaine or Ketamine on Interleukin-6 Levels in Patients Undergoing Colorectal Surgery for Cancer: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 18 Nov 2025

Brief summary (registry, in English)

Patients undergoing open colorectal surgery were randomly divided into two groups: Intravenous Lidocaine (IV-Lido) vs Intravenous Ketamine (IV-Keta). For the IV-Lido group, patients received a loading dose of Lidocaine than a continuous infusion over twenty-four hours. For the IV-Keta goup, patients received a loading dose of Ketamine than a continuous injection of Ketamine over twenty-four hours. Plasma concentrations of Interleukin-6(IL-6) were measured preoperatively before anesthetic induction and at twenty-four hour post operatively.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
19 Jan 2024
Start date
1 Oct 2023
Primary completion date
10 Feb 2026
Lead sponsor
University Tunis El Manar
NCT number
NCT06272461

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 1 Oct 2023 to the primary completion date, 10 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Duration of surgery longer than 5 hours.

Other

  • Severe intraoperative complications.

Who the study is looking for

  • Patients aged 18 or older.
  • American society of anesthesiologists' (ASA) physical status of I-III.
  • Elective open colorectal surgery.
    • NON INCLUSION CRITERIA:
  • Patients with contraindications to lidocaine or ketamine.
  • Corticosteroid therapy within the last 6 months.
  • History of immunosuppressive therapy.
  • History of surgery in the last 3 months.
  • Personal medical history of inflammatory bowel disease.
  • Personal medical history of cardiac arrythmias or conduction disorders.
  • Alcohol or drug abuse.
  • Chronic use of opioids or benzodiazepines.

Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tunisia
Coordinator of this site? Confirm its status
NabeulTunisiaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.