The aim of the study is to assess improvement in visual evoked potential, cognition, fatigue, micturation and walking impairment under 3 months of Fampyra treatment
Study Type
OBSERVATIONAL
Enrollment
50
The will be given as per normal patient treatment plan
Vestre Viken Helseforetak
Drammen, Norway
RECRUITINGchange from baseline in visual evoked potential after 2 weeks and 3 months
Time frame: 5 months
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