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Physical Disability in Patients Treated With Betaferon

Multiple Sclerosis Clinical Trial

Official title:
Physical Disability Observational Study in Patients Treated With Betaferon in Daily Practice

Clinical Trial Summary

To gather Observation data about physical disability progression, safety and adherence during the use of Betaferon in daily practice. Patients with any type of Multiple Sclerosis (MS) (MRRS) (PSMS), under treatment with Betaferon.Open Multicentric Observational study.24 months.Evaluation of physical disability in patients treated with Betaferon, using Kurtzke's expanded disability scale (EDSS) in biannual periods

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00873340
Study type Observational
Source Bayer
Contact
Status Completed
Phase N/A
Start date October 2007
Completion date January 2011
View Details
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