CompletedPhase 2MS (type not specified)NCT03740295

What it found

Result in a paper, not read yet

A paper reports the results; we have not read it yet. See Papers below.

What was tested

Treatment tested

  • Wax, emulsifying

Placebo or sham

  • Placebo

What it measured

Main measures

  • Lipid peroxidation Malondialdehyde (MDA)

    0-4 months

  • Tumor necrosis factor alfa (TNF-alpha)

    0-4 months

    Immune responseHow the body handles the medicine
  • Interleukin 6 (IL-6)

    0-4 months

    Immune responseHow the body handles the medicine

Other measures (27)

  • Quantitative electroencephalogram (QEEG)

    0-4 months

    Physical function
  • Betahydroxybutyrate

    0-4 months

  • C-reactive protein

    0-4 months

  • Haptoglobin

    0-4 months

  • Field oxide (FOX)

    0-4 months

  • Total antioxidants (TEAC)

    0-4 months

  • Copper reduction capacity (CUPRAC)

    0-4 months

  • Iron reduction capacity (FRAP)

    0-4 months

  • Paraoxonase 1 (PON1)

    0-4 months

  • Anxiety

    0-4 months

    Mood and sleep

Who could take part

MS (type not specified) · 19 to 65

Inclusion Criteria: * Multiple Sclerosis patients older than 19 years ans under 65 who sign informed consent of the study Exclusion Criteria: * Patients with coconut oil intolerance or other chronic metabolic pathologies

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

Based on the fact that the fundamental pathogenic mechanism of the Multiple Sclerosis (MS) disease is neuroinflammation, related in turn to cellular oxidation and mitochondrial alterations, this project aims to assess the impact of a nutritional intervention on the evolution of MS patients in their different slopes. To this end, the administration of medium-chain triglycerides, whose metabolism produces the increase of ketone bodies in the blood, will be carried out; and another of the antioxidant polyphenol epigallocatechin gallate. This procedure will be applied over 6 months, based on a isocaloric Mediterranean diet, with a population for the study of 80 patients with different variants of the disease. The assessment of the intervention will be carried out every two months, at motor-functional, anthropometric, cognitive and emotional, inflammatory, and oxidation levels.

Papers

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Related trials

History

    1. Started

      Oct 2018

    2. Main results due

      Jan 2019

    3. Finished

      Feb 2019

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