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Clinical Trial Summary

The primary objective of this study is to determine the normative range of brain volume and brain volume change in healthy control (HC) participants whose age, race, and gender distribution is approximately matched to the age, race, and gender distribution of patients with Multiple Sclerosis (MS) enrolled in Study 888MS001. The secondary objective is to use the results of the primary endpoint to ensure consistency of brain volume measurements across MS PATHS centers.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02996084
Study type Observational
Source Biogen
Contact
Status Active, not recruiting
Phase
Start date December 12, 2017
Completion date December 15, 2022

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