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Clinical Trial Summary

The purpose of this study is to demonstrate the superiority of propionic acid over placebo as add on treatment in multiple sclerosis (MS).


Clinical Trial Description

This is a single-center, double-blinded, randomized trial. One hundred multiple sclerosis (MS) patients will be randomly assigned in a 2:1 ratio to receive either 100 mg of propionic acid or a placebo over a period of 90 days. Outcome measures will encompass NfL and GFAP levels, fatigue scores, quality of life assessments, and physical examinations. Additionally, subgroup analysis will involve the evaluation of MRI and MEG data. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06402487
Study type Interventional
Source Salzburger Landeskliniken
Contact
Status Enrolling by invitation
Phase Phase 2/Phase 3
Start date May 1, 2024
Completion date October 15, 2024

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