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Myopathy Registry Berlin

Myopathy Registry Berlin - MyoReg

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033202
Enrollment
2000
Registered
2024-01-25
Start date
2022-03-11
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

myopathies

Interventions

Group 1: All standardized, systematically collected interdisciplinary clinical and paraclinical data of patients with myopathies who present at the outpatient clinic for muscle diseases of the Charité

Sponsors

Universitätsmedizin Charité
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Female and male individuals over 18 years of age diagnosed with myopathy. The diagnosis can be made clinically, histopathologically and/or human genetically. Signed informed consent.

Exclusion criteria

Exclusion criteria: Age <18 years Lack of informed consent

Design outcomes

Primary

MeasureTime frame
The aim of the current project is to record patients with myopathies using a standardized data set in a registry in which systematically collected interdisciplinary clinical and paraclinical data is brought together. This will create the prerequisites for a national or international data set for the use of AI-based analysis tools.

Secondary

MeasureTime frame
see above

Countries

Germany

Contacts

Public ContactKatrin Hahn

Universitäsmedizin Charité

katrin.hahn@charite.de0049 30 450660049 oder

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026