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Clinical Trial Summary

The study aims to assess the validity of real-world activity monitoring by the Syde® wearable device in subjects with multiple slclerosis. The Syde® collected data will be compared to on-site conventional clinical endpoints for MS pathology (EDSS, FSS and T25FWT). Subjects with multiple sclerosis will be assessed every 6 months for 2 years.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06346704
Study type Observational
Source SYSNAV
Contact
Status Active, not recruiting
Phase
Start date April 25, 2024
Completion date November 30, 2026

See also
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