Skip to content

The German Multiple Sclerosis Registry of the German MS Society

The German Multiple Sclerosis Registry of the German MS Society - MS-Register

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00011257
Enrollment
50000
Registered
2016-11-11
Start date
2003-06-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

G35 G37.8 G04.9 G04.8

Interventions

Group 1: The MS-Register is an oberservational study. Routine examinations are done as specified by the attending physician depending on the individual disease course of the patient. Documentation con

Sponsors

MS Forschungs- und Projektentwicklungs-gGmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - MS as defined by McDonald Criteria or clinical isolated syndrom - written informed consent - primary residence in Germany

Exclusion criteria

Exclusion criteria: - non determinable MS disease course (except CIS) - missing ability to consent

Design outcomes

Primary

MeasureTime frame
collected Data: - the socio-economic status of the patients - distribution of disease forms - symptoms and their treatments - the kind of care that is received by the PwMS - if and the kind of treatment the PwMS receive - how long it takes to diagnose - disability-status - adverse events - pregnancies

Secondary

MeasureTime frame
in add-on modules data on DMD-usage is collected

Countries

Germany

Contacts

Public ContactMS-Register Team

MS Forschungs- und Projektentwicklungs-gGmbH

kontakt@msregister.de+49 511 444 599 55

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026