Multispectral optoacoustic tomography (MSOT) for translational molecular imaging in neuromuscular disease
Recruiting
- Conditions
- Pompe Disease Myositis Hereditary myopathies Spinal muscular atrophy
- Registration Number
- DRKS00033110
- Lead Sponsor
- niversitätsmedizin Göttingen, Klinik für Neurologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 85
Inclusion Criteria
Certain diagnosis of a neuromuscular disease evaluated in this study.
Able to give consent to the study
Exclusion Criteria
Uncertain neuromuscular disease, diagnosis of neuromuscular disease not evaluated in this study.
Inability to give consent
Pregnancy
Tattoos in the examinated skin area
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of differences in muscle structure profiles between different neuromuscular diseases (SMA, hereditary myopathies, myositis, Pompe Disease) in MSOT and possibility of differentiating between disease entitites.
- Secondary Outcome Measures
Name Time Method Comparison of quantitative glycogen, lipide, collagen and haemoglobin portions between different neuromuscular diseases compared to healthy controls. Evaluation of correlation between structural markers and disease severity.