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Completed

NCT Number: NCT03797937

Microbiome Benchmarking to Identify Perturbations in Multiple Sclerosis II

The goal of this longitudinal study is to (1) explore the association between the gut microbiota and inflammatory disease activity in early onset multiple sclerosis, (2) investigate whether/how gut microbial composition vary when patients experience a relapse, and (3) to assess whether the gut microbiota shows increased similarities between affected pairs of first-degree relatives within the same family when compared with discordant pairs of first-degree relatives.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universitair Ziekenhuis Brussel, Jette, Brussels Capital, Belgium

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About this study

Using metagenomics, as well as clinical, immunological, and radiological observations, the investigators will investigate if active relapsing-remitting multiple sclerosis patients have a more pro-inflammatory gut microbiota signature than multiple sclerosis patients with less active disease and matched healthy controls.

More specifically, the investigators will investigate whether temporal variability of the gut microbiota is related to inflammatory disease activity in multiple sclerosis, whether changes in the gut microbiota are predictive of future inflammatory disease activity in multiple sclerosis, and whether gut microbiota characteristics are predictive of the disease course after 2 years.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

patients:

  • Diagnosis of MS (as defined by the 2010 McDonald criteria).
  • Occurrence of symptoms no longer than 5 years before baseline.
  • Aged 18-65.
  • Willingness to participate in the study and to sign the informed consent.

Exclusion criteria

patients:

  • Treatment with high doses of systemic steroids 2 months before baseline.
  • Use of antibiotics 3 months before baseline.
  • Chronic gastrointestinal disease (e.g. inflammatory bowel disease, colon cancer).
  • Other immune-mediated or autoimmune diseases (e.g. rheumatoid arthritis, diabetes type 1 and 2, psoriasis).

Additional inclusion criteria for MS patients undergoing a relapse:

  • Ability to provide a faecal sample within 4 weeks from onset of the first symptoms suggestive of a relapse, before cortisone treatment. A relapse is defined by a new clinical sign or clinical worsening of a previous sign/symptom persisting for >=24 hours in the absence of fever.

Additional exclusion criteria for MS patients undergoing a relapse:

  • Treatment with cortisone before collection of baseline faecal sample.
  • Evidence of a relapse less than 2 months before baseline.
  • Switching disease modifying treatment less than 2 months before baseline.

Inclusion criteria

healthy controls:

  • Willingness to participate to the study and to sign the informed consent.
  • Aged >=18.

Exclusion criteria

healthy controls:

  • Neurodegenerative disorders.
  • Chronic gastrointestinal disease (e.g. inflammatory bowel disease, colon cancer) or autoimmune diseases (e.g. rheumatoid arthritis, diabetes type 1, psoriasis).
  • Use of antibiotics 3 months before baseline.
  • Treatment with high doses of systemic steroids 2 months before baseline.

Treatment and study plan

magnetic resonance imaging (MRI)

Other

MRI scanner

Primary outcomes

  1. Clinical evidence for active disease

    Time frame: 3 years

    Time to first relapse (after baseline) will be reported for all patients.

Secondary outcomes

  1. Radiological evidence for active disease

    Time frame: 3 years

    Occurrence of new contrast-enhancing T1 hyper intense lesions, or changes in white matter lesion volume (i.e. new or enlarging T2 hyper intense lesions)

Sponsors and collaborators

Lead sponsor

National MS Center Melsbroek

Other

Registry information

Important dates

Study start
2018
Primary completion
2021
Study completion
2022
First posted
Jan 9, 2019
Registry last updated
May 11, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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