Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Preoperative Ketogenic Diet to Reduce Fat in the Liver Before Surgery

Official title: Implementation of a Preoperative Ketogenic Diet for Reduction of Hepatic Steatosis Prior to Hepatectomy: a Randomized Control Trial

Run by Western University, Canada · NCT05884723 · Data updated 2026-11-12

This study tests whether a short, very low-carbohydrate ketogenic diet before liver surgery can reduce liver fat and improve surgical outcomes for patients with liver metastases from colorectal cancer and NAFLD.

More NAFLD trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment124 (estimated)
SponsorWestern University, Canada
Academic / other
Locations1 site (London, Ontario)
StatusRecruiting
StartedMay 1, 2024
Main results expectedDecember 2027
Study endsDecember 2032
Registry record updatedMay 19, 2026
Trial IDNCT05884723 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older with NAFLD or hepatic steatosis undergoing liver resection for colorectal liver metastases and able to use a nutrition-tracking app.

Probably not a fit

Patients without hepatic steatosis, those not undergoing planned liver resection, or those unable to follow a very low-carbohydrate diet may not benefit.

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

What this trial studies

This randomized trial compares a 4-week preoperative ketogenic diet to standard dietary consultation in patients with fatty liver undergoing liver resection for colorectal liver metastases. All participants track their intake with a nutrition app, and outcomes include intraoperative blood loss and operating room time, as well as postoperative complications. The aim is to see if lowering liver fat before surgery improves perioperative and disease outcomes. No drug interventions are used; the intervention is a structured diet supervised by dietitians. The study is conducted at London Health Sciences Centre/Western University with lead sponsor Anton Skaro.

Why it matters

Potential benefit: If successful, a preoperative ketogenic diet could reduce surgical risks and improve recovery for patients with fatty liver undergoing liver surgery.

How similar studies have gone: Previous studies suggest liver fat can be reduced with diets, but randomized trials of a preoperative ketogenic diet for liver surgery are limited, making this approach relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients 18 years of age or older undergoing any type of liver resection (e.g. wedge, formal hepatectomy), either open or laparoscopic, for colorectal liver metastases (CRLM)
* Patients with evidence of hepatic steatosis on pre-operative imaging (CT or MR) or biopsy.
* Ability to use an app based nutritional program to track macronutrient uptake throughout the dietary intervention.

Exclusion Criteria:

* Patients undergoing liver resection for any other indication
* Patients on sodium glucose co-transporter 2 (SGLT-2) inhibitors (these are contraindicated with a ketogenic diet).
* Patients without evidence of hepatic steatosis.
* Patients with evidence of liver fibrosis or cirrhosis on preoperative bloodwork or imaging.
* Patients with alcohol-related hepatic steatosis.
* Patients with a known bleeding disorder.

Where it's running

  • London Health Sciences Centre/Western University
    London, Ontario, Canada
    Recruiting

Study contacts

  • Principal investigator: Anton Skaro, MD PhD — London Health Sciences Centre/Lawson Health Research Institute
  • Study coordinator: Anton Skaro, MD PhD
  • Email: Anton.Skaro@lhsc.on.ca
  • Phone: 519-685-8500

Similar studies

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

  • Can hepatic artery infusion chemotherapy enable liver surgery for colorectal cancer that has spread to the liver?

    This study tests whether hepatic artery infusion chemotherapy plus standard chemotherapy can make some inoperable colorectal liver metastases operable in patients.

    Recruiting Phase 2 Sunnybrook Health Sciences Centre · Toronto, Ontario · NCT07764497

  • Non-invasive blood and imaging tests for metabolic liver disease

    This project tests whether blood tests and imaging scans can diagnose and stage metabolic-associated steatohepatitis (MASH) and liver fibrosis in adults with metabolic risk factors.

    Recruiting at 4 sites Foundation for the National Institutes of Health · Miami, Florida and 3 other locations · NCT07122700

  • Low‑methoxy pectin for inflammation, gut microbiome, and metabolic health in MASLD

    This tests whether taking daily low‑methoxy pectin for six weeks can reduce inflammation and improve gut bacteria and metabolic markers in adults with MASLD.

    Recruiting at 3 sites University of Nottingham · Nottingham, United Kingdom and 2 other locations · NCT07093346

  • CRISPR-edited donor liver transplant to reduce rejection

    This trial will try transplanting deceased-donor livers that have had key HLA genes removed with CRISPR to see if they cause less rejection in adults needing a liver transplant.

    Recruiting Phase 1/2 American Organ Transplant and Cancer Research Institute LLC · Beijing, Changping · NCT07053488

  • Prospective NAFLD/NASH patient cohort and biobank

    This project will collect medical data and blood/tissue samples from adults with NAFLD/NASH to create a long-term resource to help researchers understand disease course and causes.

    Recruiting Fondazione Epatocentro Ticino · Lugano, Canton Ticino · NCT07051863

  • Digital prevention for liver disease management

    This study is testing a new way to help people with liver disease by using a mobile app for patients and a dashboard for doctors to see if it improves their care and health outcomes.

    Recruiting Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Rome, Lazio · NCT06879236

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.