Overview

Efficiency of 4-aminopyridin (Fampyra) on Gait, Vision, Cognition, Fatigue and Micturation in Patients With Multiple Sclerosis

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
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
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Vestre Viken Hospital Trust
Criteria
Inclusion Criteria:

All patients who according to the compound's Norwegian prescription guidelines are deemed
eligible for the study, i.e. MS patients with impaired walking as determined by an EDSS
4-7. They do not need a past history of optic neuritis, cognitive failure, fatigue or
difficulties micturating.

Exclusion Criteria:

MS patients with contraindications to the compound according to the prescription
guidelines.

Patients who have been exposed to Fampyra in the past Patients with an MS attack within
last 3 months