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NCT06715436Recruiting

Multiple Sclerosis and the Effects of Ketogenic Diet Therapy

The Effects of Ketogenic Diet Therapy Versus the Mediterranean Diet on Quality of Life in a Group of Patients With Multiple Sclerosis - the KETOMED-MS Study

Source: ClinicalTrials.gov · Last updated 20 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Multiple sclerosis (MS) is an inflammatory and immune-mediated neurological disease with multifactorial etiology. The specific etiopathogenetic mechanisms of MS are still unknown but it is clear that it results from a combination of genetic and environmental factors. Several studies have reported the possible role of diet as a risk factor for MS and its progression. To date, many dietary patterns and their association with MS have been studied, but data is still limited and inconclusive. Mediterranean Diet (MedDiet) has been associated with a lower risk of developing MS, compared to a Western-style diet. In one of investigators' studies, higher MedDiet adherence was associated with a 6-fold greater likelihood of having lower disease severity than those with low adherence. A significant restriction of carbohydrates (up to ketogenesis) can have beneficial effects on various parameters (inflammatory markers, oxidative stress, altered glucose metabolism) which are altered in subjects with MS. Ketogenic diet therapies (KDTs) have been recommended mainly for children with drug-resistant epilepsy, but in recent years they have been applied to Multiple Sclerosis. Preclinical studies in animal models evaluating the efficacy of KDTs in experimental autoimmune encephalomyelitis (EAE) found a beneficial effect of diet in slowing of disease progression, improvement of motor disability, reduction of inflammatory cytokines and reactive oxygen species. In a randomized study, improvements in health-related quality of life (HRQL) scores and a slight decrease in EDSS scores were found. An open-label, single-arm study of 20 patients with RRMS also reported that, after 6 months of MAD, no subjects had new or enlarging FLAIR/T2 lesions, with a significant improvement in the EDSS score, the Modified Fatigue Impact Scale subscales and arm. A 3-arm parallel-arm randomized controlled pilot study was planned to determine the effectiveness of a modified Atkins diet (MAD) compared to a Mediterranean diet (MedDiet) on quality of life in a population with MS.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
111 (estimated)
First submitted
28 Nov 2024
Start date
15 Mar 2024
Primary completion date
15 Mar 2025
Lead sponsor
IRCCS National Neurological Institute "C. Mondino" Foundation
NCT number
NCT06715436

What you commit to

  • Study type: Interventional
  • Planned participants: 111
  • From 15 Mar 2024 to the primary completion date, 15 Mar 2025
  • 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

  • Relapse or cortisone treatment within 30 days before study entry
  • Weight loss greater than 5 kg within 2 months prior to study entry
  • Oral anticoagulant therapy
  • Known alcohol and drug abuse
    • Telephonic interviews will be performed monthly to evaluate adherence to the dietary treatment and/or whether any changes in supplements use, physical activity, nutrition habits.

Other illness

  • Clinically relevant metabolic, progressive or malignant diseases
  • Significant cognitive-cooperative impairment
  • Insulin-dependent diabetes mellitus (type I)
  • Diagnosis or suspicion of an eating disorder

Other

  • Patients actively engaged in a weight loss program or other specific diet (e.g. vegetarian, vegan); patients not willing to follow the assigned dietary pattern or patients with high adherence to MedDiet (MediLite score \> 14)
  • Pregnancy or breastfeeding
  • Intake of \> 1 g/day of omega-3 fatty acid supplements
  • Underweight (BMI\<18.5 kg/m2) or severe obesity
  • Kidney stones

Who the study is looking for

  • Diagnosis of relapsing-remitting MS (RRMS) or progressive MS (PMS)
  • Age between 18 and 60 years
  • BMI between 18.5 kg/m2 and 39.9 kg/m2
  • If on disease-modifying drugs, stable for 6 months, or no use of drugs in the previous 6 months
  • Ability to give verbal and written consent

Age in the registry: 18 years to 60 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
U.O.Sclerosi Multipla
Coordinator of this site? Confirm its status
PaviaItalyRecruiting

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