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Dynamic monitoring of disease progression in Multiple System Atrophy patients by serum NFL

Prospective, observational, cohort study on dynamic monitoring of disease progression in MSA patients by serum NFL

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037597
Enrollment
Unknown
Registered
2020-08-29
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

Multiple System Atrophy

Interventions

Sponsors

Shanghai First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. symptomatic group: (1) Aged 50 to 65 years old; (2) meet the diagnostic criteria of multiple system atrophy established by the International Association of dyskinesia (MDS) in 2008; (3) The fourth part of UMSARS: general disability level 21; (5) Sign informed consent; 2. prodromal patients group: (1) Aged 50 to 60 years old; (2) Patients with rapid eye movement sleep disorder or postural hypotension meeting the diagnostic criteria of PSG; (3) There were no obvious symptoms and signs of extrapyramidal system and cerebellar system that could be observed clinically; or: there were no obvious symptoms and signs of extrapyramidal system or cerebellar system, and doctors could check the signs of extrapyramidal system (updrsiii score 26 points; (5) Sign informed consent. 3. healthy control group: (1) Aged 50 to 65 years old; (2) None of the above-mentioned symptomatic patients and prodromal patients were included in the inclusion criteria; There was no disease listed in the following exclusion criteria; (3) MMSE > 26; (4) Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with Parkinson's disease, Vascular Parkinson's syndrome, stroke, multiple sclerosis, neuromyelitis optica, motor neuron disease, vascular dementia, hydrocephalus, Alzheimer's disease, severe mental disease, encephalitis sequelae, autoimmune encephalitis, adrenoleukodystrophy, subacute combined degeneration, radiation encephalopathy and malignant tumor; 2. Patients with severe peripheral neuropathy, spinal cord injury, brain trauma, history of brain surgery, diabetes mellitus, nephrotic syndrome, uremia, severe spinal degenerative disease, and rapidly progressive leukoaraiosis; 3. Syphilis and HIV infected patients; 4. Patients who are considered unsuitable for this study by other researchers.

Design outcomes

Primary

MeasureTime frame
Neurofilament light;

Countries

China

Contacts

Public ContactZhang Xiaojin

Shanghai First People's Hospital

kokolalazxj@163.com+86 13918296517

Outcome results

None listed

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