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Multi-Center Study of Natural History in Atypical Parkinsonian Syndromes (MAPS-NH)

Multi-Center Study of Natural History in Atypical Parkinsonian Syndromes (MAPS-NH)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07805967
Enrollment
500
Registered
2026-09-08
Start date
2025-11-12
Completion date
2030-08-31
Last updated
2026-09-08

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

Conditions

Corticobasal Degeneration (CBD), Dementia With Lewy Bodies (DLB), Multiple System Atrophy, Progressive Supranuclear Palsy (PSP)

Brief summary

This goal of this observational study is to clarify the variations in the natural course of atypical parkinsonian syndromes (APS, including MSA, DLB, PSP, and CBD), such as the progression rate of motor and non-motor symptoms and characteristic imaging evolution patterns. Establish a comprehensive assessment framework for APS, and develop clinical and biological databases to identify biomarkers with early predictive value.

Interventions

OTHERWe did not apply any interventions; only observational research was conducted.

We did not apply any interventions; only observational research was conducted.

Sponsors

Second Affiliated Hospital of Soochow University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. MSA : Meets the "probable MSA" criteria in the 2022 Chinese expert consensus on MSA diagnosis (MSA-P or MSA-C subtype); disease duration ≤3 years (from onset of first motor symptoms) . 2. DLB : Meets "probable DLB" criteria per the 2017 McKeith diagnostic criteria; MMSE ≥18 (to exclude severe dementia confounding assessment) . 3. PSP : Meets "probable PSP-Richardson syndrome" criteria per the 2017 PSP diagnostic standards; vertical gaze palsy or postural instability with duration ≤2 years . 4. CBD : Meets "probable CBD" criteria per the 2019 Chinese expert consensus on corticobasal degeneration diagnosis and treatment; asymmetric cortical symptoms (apraxia/dystonia/alien limb).

Exclusion criteria

1. Parkinson's disease , spinocerebellar ataxia (SCA) and other secondary autonomic failure . 2. Vascular parkinsonism , Parkinsonism caused by stroke , tumor , or immune-mediated encephalitis .

Design outcomes

Primary

MeasureTime frameDescription
Natural disease progression of various atypical parkinsonian syndromesup to 36 monthsTo observe the differences in the natural disease progression of various atypical parkinsonian syndromes (APS, including MSA, DLB, PSP, and CBD), such as the progression rates of motor and non-motor symptoms and the patterns of imaging evolution. The preliminary study design involves a follow-up period of 3 years, with assessments of clinical phenotypes and/or biomarker changes every 6 months.

Countries

China

Contacts

CONTACTJinru Zhang, PhD. MD.
zhangjinruruby@126.com+8615850210657
CONTACTChunfeng Liu, PhD. MD
liuchunfeng@suda.edu.cn+86 13606210609
STUDY_CHAIRChunfeng Liu

Second Affiliated Hospital of Soochow University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 9, 2026