NL-OMON55562
Completed
N/A
A prospective, multi-centre study investigating the incidence and prognosis of relapses, pseudo-relapses and other causes of (sub)acute neurological symptoms in patients with relapsing-remitting multiple sclerosis. - RELAMS study
Sint Elisabeth Ziekenhuis0 sites125 target enrollmentTBD
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Sint Elisabeth Ziekenhuis
- Enrollment
- 125
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
Trial is onging in other countries
Investigators
Eligibility Criteria
Inclusion Criteria
- •\* The subject must give written informed consent
- •\* The subject is between the age of \*18 and \*55 years
- •\* The subject suffers from RRMS or CIS
- •\* The subject has an EDSS of 5\.5 or less prior to baseline (e.g. ambulatory
- •without aid for about 100 meters)
- •\* The subject has experienced (sub)acute neurological symptoms within 14 days
- •before visit
- •\* The subject must be prepared to and considered able to follow the protocol
- •during the whole trial period and to attend the planned visits
Exclusion Criteria
- •\* The subject has received treatment with glucocorticoids within one month
- •prior to the inclusion in the study
- •\* The subject has experienced a relapse within one month prior to inclusion in
- •\* The subject has already been included in this study during a previous episode
- •of symptoms
Outcomes
Primary Outcomes
Not specified
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