Actively Recruiting
Swiss Multiple Sclerosis Cohort-Study
Led by University Hospital, Basel, Switzerland · Updated on 2025-04-14
1200
Participants Needed
8
Research Sites
1543 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Basel, Switzerland
Lead Sponsor
C
Cantonal Hospital of Aarau, Switzerland
Collaborating Sponsor
AI-Summary
What this Trial Is About
The Swiss MS Cohort Study (SMSC) is a multicentre cohort study that involves 8 Swiss Multiple Sclerosis centres. The key aims of the SMSC are 1. To maintain a long-term cohort for an undefined duration of patients with Multiple Sclerosis (MS), neuromyelitis optica spectrum disorder (NMOSD) and Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) in Switzerland. This requires effective measures to limit drop-outs and the continuous recruitment of MS patients and 2. To conduct a systematic follow-up with standardized, high quality collection of clinical and magnetic resonance imaging (MRI) data, as well as body fluids. The significant heterogeneity within the diagnostic entity and phenotype of MS is incompletely understood. A central and necessary prerequisite of further advance is a sufficient amount of high quality clinical and paraclinical (imaging, body fluids) patient data. Nested projects will address specific research topics, and facilitate collaboration of the most qualified investigators within the group of SMSC investigators. The nested projects will focus on the: 1. Development and validation of diagnostic and prognostic markers of spontaneous disease evolution and therapeutic response. 2. Exploration of the safety and impact on long-term disability of existing and next generation MS treatments 3. Individualized therapy: A number of highly active but potentially also harmful therapies have lately been established for the treatment of MS. To date, due to the lack of individual prognostic markers patients may not receive aggressive therapy due to safety concerns, or patients with benign disease may receive expensive and potentially harmful treatments without the need for it. 4. Evaluation of intervention effects by conducting embedded pragmatic trials using the SMSC as data-infrastructure.
CONDITIONS
Official Title
Swiss Multiple Sclerosis Cohort-Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with radiologically isolated syndrome (RIS), clinically isolated syndrome (CIS), relapsing-remitting Multiple Sclerosis (RRMS), secondary-progressive MS (SPMS), primary-progressive MS (PPMS), neuromyelitis optica spectrum disorder (NMOSD), or Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) according to established criteria
- Intends to attend hospital visits every 6 months (+/- 45 days) or 12 months (+/- 45 days) with optional cranial MRI every 12 months for at least 5 years
- Intends to provide blood samples for biobanking every 6 or 12 months during hospital visits or within +/- 8 days
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 8 locations
1
Cantonal Hospital Aarau
Aarau, Canton of Aargau, Switzerland, 5001
Actively Recruiting
2
University Hospital Basel
Basel, Canton of Basel-City, Switzerland, 4031
Actively Recruiting
3
University Hospital Berne
Bern, Canton of Bern, Switzerland, 3010
Actively Recruiting
4
University Hospital Geneva
Geneva, Canton of Geneva, Switzerland, 1211
Actively Recruiting
5
Cantonal Hospital St. Gallen
Sankt Gallen, Canton of St. Gallen, Switzerland, 9007
Actively Recruiting
6
University Hospital Lausanne
Lausanne, Canton of Vaud, Switzerland, 1011
Actively Recruiting
7
Regional Hospital Lugano
Lugano, Canton Ticino, Switzerland, 6900
Actively Recruiting
8
Univeristy Hospital Zürich
Zurich, Switzerland
Actively Recruiting
Research Team
J
Jens Kuhle, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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