Clinical trial Recruiting at 1 site Interventional Ages 18 to 90

Comparing Lidocaine and Ketamine for Pain Management in Colorectal Surgery

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

Run by University Tunis El Manar · NCT06272461 · Data updated 2026-11-12

This study is testing whether intravenous Lidocaine or Ketamine works better for managing pain and reducing inflammation in patients having open colorectal surgery.

More Colorectal (Colon or Rectal) Cancer trials

Quick facts

Study typeInterventional
Ages18 Years to 90 Years
SexAll
Enrollment50 (estimated)
SponsorUniversity Tunis El Manar
Academic / other
Locations1 site (Nabeul)
StatusRecruiting
StartedOctober 1, 2023
Main results expectedFebruary 10, 2026
Study endsMarch 30, 2026
Registry record updatedNovember 18, 2025
Trial IDNCT06272461 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 or older who are scheduled for elective open colorectal surgery and have an ASA physical status of I-III.

Probably not a fit

Patients with contraindications to lidocaine or ketamine, or those with a history of certain medical conditions or recent surgeries, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the effectiveness of intravenous Lidocaine versus intravenous Ketamine in managing pain for patients undergoing open colorectal surgery. Participants are randomly assigned to receive either a loading dose followed by a continuous infusion of Lidocaine or Ketamine over a 24-hour period. The study measures plasma concentrations of Interleukin-6 (IL-6) before and after surgery to assess the inflammatory response associated with each treatment. The goal is to determine which medication is more effective in reducing postoperative inflammation and pain.

Why it matters

Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing colorectal surgery.

How similar studies have gone: Other studies have shown promising results with similar approaches using intravenous anesthetics for pain management, suggesting potential for success in this trial.

Who can join: the full rules

Show full inclusion / exclusion criteria
INCLUSION CRITERIA:

* 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.

EXCLUSION CRITERIA:

* Severe intraoperative complications.
* Duration of surgery longer than 5 hours.

Where it's running

  • Tunisia
    Nabeul, Tunisia
    Recruiting

Study contacts

  • Principal investigator: BEN ALI MECHAAL, Professor — university manar Tunis, Tunisia
  • Study coordinator: BEN ALI MECHAAL, Professor
  • Email: mechaal_benali@yahoo.fr
  • Phone: 72100533

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.