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Diagnostic relevance of myosonography in hereditary myopathies

Diagnostic relevance of myosonography in hereditary myopathies - Myosonography in hereditary myopathies

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033629
Enrollment
80
Registered
2024-02-19
Start date
2023-08-03
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

G71.0 G71.1

Interventions

Group 1: With the patients consent, a single sonographic examination is performed on defined muscles of all four extremities muscles of all four extremities, as well as the trunk, respiratory, swallow

Sponsors

Universitätsmedizin Göttingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patient with a clinically and instrumentally confirmed myopathy as listed above - = 18 years of age - Ability to give consent

Exclusion criteria

Exclusion criteria: - Patient with unclear neuromuscular disease without definite classification of the disease - <18 years of age - Patient not able of giving consent

Design outcomes

Primary

MeasureTime frame
Characterisation of the different myopathies with regard to the Distribution pattern of abnormalities in muscle ultrasound (pattern)

Secondary

MeasureTime frame
Measure of the abnormalities in the muscle sonography in correlation to the - Strength levels - Limitations in everyday life - Pain symptoms

Countries

Germany

Contacts

Public ContactJana Zschüntzsch

Universitätsmedizin Göttingen

j.zschuentzsch@med.uni-goettingen.de+49 551 39 14139

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026