ClinicalTrials.gg
RecruitingNCT07805967Updated Sep 8, 2026

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

An observational study in Multiple System Atrophy, Dementia With Lewy Bodies (DLB) and Progressive Supranuclear Palsy (PSP), sponsored by Second Affiliated Hospital of Soochow University. Recruiting at 20 sites in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-08.

Sponsored by Second Affiliated Hospital of Soochow University · Observational

From the registry’s dates

  • Started Nov 2025; still recruiting 11 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Multiple System Atrophy
  • Dementia With Lewy Bodies (DLB)
  • Progressive Supranuclear Palsy (PSP)
  • Corticobasal Degeneration (CBD)
03

In context

Multiple System Atrophy

207 studies on the registry are indexed under Multiple System Atrophy; 73 are open to participants now.

This study's planned enrollment of 500 is above the median of 196 across 67 observational studies indexed under Multiple System Atrophy.

Browse Multiple System Atrophy studies →

Lead sponsor

Second Affiliated Hospital of Soochow University is the lead sponsor of 60 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients diagnosed with multiple system atrophy (MSA) , dementia with Lewy bodies (DLB) , progressive supranuclear palsy (PSP) , or corticobasal degeneration (CBD) according to Chinese/international consensus diagnostic criteria . Follow-up period : 3 years , with clinical phenotypes and/or biomarkers assessed every 6 months .

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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; ≥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

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 .
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

MMSE and MoCA

Short tests of memory and thinking, each scored out of 30. Lower scores suggest more difficulty; criteria give a range, either to include people with memory problems or to leave them out.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Target follow-up
3 Years
Patient registry
Yes

Groups and cohorts

  • Atypical parkinsonian syndromes

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

Interventions

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

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

06

What researchers measure

Primary outcomes

  1. Natural disease progression of various atypical parkinsonian syndromes

    To 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.

    Time frame: up to 36 months

07

Study locations

6 of 20 sites recruiting
  • Changshu Hospital Affiliated to Nanjing University of Chinese Medicine
    Changshu, Jiangsu 215500, China
    Recruiting
  • The second People's Hospital of Huai'an
    Huai'an, Jiangsu 223001, China
    Not yet recruiting
  • The First People's Hospial of Kunshan
    Kunshan, Jiangsu 215300, China
    Not yet recruiting
    • Qing, Tang · Contact+8618862390859
  • Jiangsu Province Official Hospital
    Nanjing, Jiangsu 210000, China
    Not yet recruiting
  • The Second Affiliated Hospital of Nantong University
    Nantong, Jiangsu 226000, China
    Not yet recruiting
    • Jia Li · Contact+8613813605009
  • Jiangsu Province (Suqian) Hospital
    Suqian, Jiangsu 223800, China
    Recruiting
    • Dan Li · Contact+8613776468080
  • The Forth Affiliated Hospital of Soochow University
    Suzhou, Jiangsu 215000, China
    Recruiting
  • The Second Affiliated Hospital of Soochow University
    Suzhou, Jiangsu 215000, China
    Recruiting
  • The Second Affiliated Hospital of Xuzhou Medical University
    Xuzhou, Jiangsu 221000, China
    Not yet recruiting
  • Yancheng Third People's Hospital
    Yancheng, Jiangsu 224000, China
    Recruiting
    • Haihua Sun · Contact+8615295370576
  • Affiliated Hospital of Yangzhou University
    Yangzhou, Jiangsu 225000, China
    Not yet recruiting
  • Zhangjiagang TCM Hospital Affiliated to Nanjing University of Chinese Medicine/Zhangjiagang Traditional Chinese Medicine Hospital
    Zhangjiagang, Jiangsu 215600, China
    Not yet recruiting
  • The Forth People's Hospital of Zhenjiang
    Zhenjiang, Jiangsu 212000, China
    Recruiting
    • Jinjun Qian · Contact+8615358595730
  • Yantai Yuhuangding Hospital
    Yantai, Shandong 264000, China
    Not yet recruiting
  • Mianyang 404 Hospital
    Mianyang, Sichuan 621000, China
    Not yet recruiting
  • Jiaxing Second Hospital
    Jiaxing, Zhejiang 314000, China
    Not yet recruiting
    • Yanping Wang · Contact+8613486331646
  • Deyang People's Hospital
    Deyang, China
    Not yet recruiting
    • Ping Zhang · Contact+8615883850268
  • Changxing people' s hospital
    Huzhou, China
    Not yet recruiting
    • Donghui Li · Contact+8615067223301
  • Affiliated Hospital of Nantong University
    Nantong, China
    Not yet recruiting
    • Xiaosu Gu · Contact13962998759
  • The Affiliated Hospital of Xuzhou Medical University
    Xuzhou, China
    Not yet recruiting
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Nov 2025 (actual). Primary completion is estimated for Aug 2030, 57 months after the start.

Of 39 observational studies under Multiple System Atrophy, half reached primary completion within 94 months of starting (the median), counting those still running; a quarter within 37. This study's planned 57 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 20, 2025
First posted
Sep 8, 2026
StartActual
Nov 12, 2025
Primary completionEst.
Aug 31, 2030
CompletionEst.
Aug 31, 2030
Last update
Sep 8, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07805967
Lead sponsor
Second Affiliated Hospital of Soochow University
Responsible party
Sponsor
First posted
Sep 8, 2026
Start date
Nov 12, 2025
Primary completion
Aug 31, 2030 (estimated)
Completion
Aug 31, 2030 (estimated)
Last update
Sep 8, 2026

Study contacts

Jinru Zhang, PhD. MD.
Contact
zhangjinruruby@126.com
+8615850210657
Chunfeng Liu, PhD. MD
Contact
liuchunfeng@suda.edu.cn
+86 13606210609 ext. +8613606210609
Chunfeng Liu
study chair · Second Affiliated Hospital of Soochow University
View the source record on ClinicalTrials.gov ↗

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