ClinConnect ClinConnect Logo
Search / Trial NCT02433028

Swiss Multiple Sclerosis Cohort-Study

Launched by UNIVERSITY HOSPITAL, BASEL, SWITZERLAND · Apr 28, 2015

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Ms Key Phases Of Disease Evolution Ms New Treatment Options

ClinConnect Summary

The Swiss Multiple Sclerosis Cohort Study (SMSC) is a research project aimed at better understanding multiple sclerosis (MS) and related conditions, like neuromyelitis optica spectrum disorder (NMOSD) and Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). The study is taking place across eight centers in Switzerland and seeks to follow a group of patients for a long time—possibly many years. Researchers will collect important information about participants' health, including regular check-ups and MRI scans, to learn more about how these diseases progress and how treatments work. They hope to find better ways to predict how a patient's disease will evolve and the effectiveness and safety of different therapies.

To participate, individuals need to have a confirmed diagnosis of one of the specified conditions and be willing to visit the hospital every six or twelve months for check-ups and blood tests. The study welcomes all genders and has no specific age limit. By joining, participants will help researchers gather valuable data that could improve treatment options for MS and related disorders, ultimately benefiting many patients in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Fulfilling the diagnosis of 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
  • Intending to attend hospital visits every 6 months (+/- 45 days) or 12 months (+/- 45 days) (facultative cranial MRI every 12 months) over a longer period (at least 5 years)
  • Intending to give blood for biobanking every 6 or 12 months during hospital visit or as close as possible to the visit (+/- 8 days)
  • Inclusion criteria are crafted to identify a population of patients with MS, NMOSD or MOGAD particularly suitable for analysing disease evolution and associated factors, treatment dynamics, and the long-term safety and efficacy profile of disease-modifying drugs.
  • There are no specific Exclusion Criteria.

About University Hospital, Basel, Switzerland

The University Hospital Basel, Switzerland, is a leading academic medical center renowned for its commitment to cutting-edge research and innovative patient care. As a prominent clinical trial sponsor, the hospital leverages its extensive expertise and state-of-the-art facilities to advance medical knowledge and therapeutic options across various disciplines. With a collaborative approach that integrates clinical practice and scientific inquiry, the University Hospital Basel fosters an environment conducive to rigorous clinical trials, ensuring the highest standards of safety and efficacy. Its strategic focus on patient-centered research aims to translate scientific discoveries into tangible health solutions, benefiting both local and global communities.

Locations

Basel, Bs, Switzerland

Lausanne, Vd, Switzerland

Geneva, Ge, Switzerland

Aarau, Ag, Switzerland

Berne, Be, Switzerland

St. Gallen, Sg, Switzerland

Lugano, Ti, Switzerland

Zürich, , Switzerland

Patients applied

0 patients applied

Trial Officials

Jens Kuhle, MD

Principal Investigator

University Hospital, Basel, Switzerland

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials