Prospective Multicenter Registry Study of Multiple System Atrophy in China
Clinical Features and Natural History of Multiple System Atrophy: A Prospective Multicenter Registry Study in China
Peking University First Hospital
214 participants
Jun 1, 2025
OBSERVATIONAL
Conditions
Summary
Multiple system atrophy is a rare, rapidly progressive neurodegenerative disease characterized by variable combinations of parkinsonism, cerebellar ataxia, and autonomic dysfunction. Existing natural history studies from North America, Europe, and Japan suggest that clinical phenotypes and disease progression may differ across populations. However, comprehensive multicenter prospective data from Chinese patients with multiple system atrophy remain limited. This prospective multicenter registry study aims to describe the clinical characteristics, longitudinal progression, and outcomes of Chinese patients with multiple system atrophy, to identify factors associated with disease progression and prognosis, and to establish a longitudinal cohort for future biomarker validation and clinical trial design.
Eligibility
Inclusion Criteria5
- Patients with clinically established or clinically probable multiple system atrophy according to the 2022 Movement Disorder Society diagnostic criteria; or
- Patients with clinically established or clinically probable Parkinson disease according to the Movement Disorder Society diagnostic criteria; or
- Healthy controls or controls without hereditary or neurodegenerative diseases who voluntarily agree to participate.
- Age between 40 and 75 years.
- Ability to provide informed consent or availability of a legally authorized representative when applicable.
Exclusion Criteria6
- Parkinsonism that cannot be classified as Parkinson disease or multiple system atrophy at the time of evaluation.
- Clinical suspicion or diagnosis of other atypical parkinsonian syndromes, including progressive supranuclear palsy, dementia with Lewy bodies, or corticobasal syndrome.
- Secondary parkinsonism due to intracranial space-occupying lesions, normal pressure hydrocephalus, drug-induced parkinsonism, or other identifiable causes.
- Comorbid diseases that may substantially affect autonomic function, such as diabetic peripheral neuropathy or amyloidosis.
- Refusal to participate in the study or refusal to undergo routine clinical evaluations for parkinsonian syndromes.
- Psychiatric or behavioral abnormalities that preclude reliable clinical data collection or scale-based assessment.
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07644013