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Clinical Trial Summary

Design: Randomized, double-blind, placebo-controlled study with 4 weeks of treatment with either fiber supplements or placebo. Primary outcome: variation in SCFA between baseline and week 4. Secondary outcomes : variations in gut microbiota, disease activity (DAS28, RAID), immune cells (regulatory T and B cells, Th17) and heart-rate variability. Population: 29 patients with rheumatoid arthritis treated with only csDMARDs and a moderate disease activity will be recruited in each arm and 29 controls with mechanic disease (osteoarthritis, tendinitis). Collection: Blood, feces, disease activity and heart rate variability will be collected at baseline and week 4.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04421313
Study type Interventional
Source University Hospital, Montpellier
Contact Claire DAIEN, MD-PhD
Phone 467332319
Email c-daien@chu-montpellier.fr
Status Recruiting
Phase N/A
Start date September 2, 2020
Completion date October 2024

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