Swiss Multiple Sclerosis Registry

NCT02980640 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2025-05-15

No results posted yet for this study

Summary

The Swiss Multiple Sclerosis Registry is a national, patient-centered registry with the aim to document the epidemiology of multiple sclerosis (MS), as well as the quality of life of persons living with MS in Switzerland.

Conditions

Sponsors & Collaborators

  • University of Zurich

    collaborator OTHER
  • Schweizerische Multiple Sklerose Gesellschaft

    collaborator OTHER
  • Swiss Multiple Sclerosis Registry

    lead OTHER

Principal Investigators

  • Milo Puhan, MD PhD · University of Zurich

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2041-06-30
Completion
2041-06-30

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02980640 on ClinicalTrials.gov