Neurodegenerative Diseases Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorVincent Mok

About this trial

With the increase in life expectancy of our population due to advancement of medical diagnosis and treatments, the incidence of age dependent neurodegenerative diseases increased, including Alzheimer's disease (AD), parkinsonian syndromes (PS), small vessel disease (SVD) and motor neuron disease (MND). In spite of the progress of knowing the pathogenesis of various neurodegenerative diseases at molecular and genetic level, they are still very incompletely understood and often cause diagnostic and therapeutic challenges to physicians. Due to the overlapping presentation and similar brain pathology, especially in the early stage of the diseases, it is difficult to differentiate idiopathic Parkinson's disease (iPD) from atypical parkinsonian syndromes, such as multiple system atrophy (MSA) and progressive supranuclear palsy (PSP). Similarly, distinguishing AD from other dementia syndromes including frontotemporal dementia (FTD), dementia with Lewy Bodies (DLB), corticobasal degeneration (CBD) and vascular dementia can be difficult. It is necessary to develop accurate and comprehensive diagnostic tests to properly prognosticate the diseases, start treatments in early stage of the diseases and maximize the accuracy of drug trials for more effective preventive and therapeutic measures for these neurodegenerative diseases.

Therefore, the registry aims to generate a large database of cognitive, behavioral, lifestyle and psychological information of the subjects who suffered from neurodegenerative diseases, as well as to examine the genetic basis of neurodegenerative diseases to help decode the pathogenic mechanisms of the diseases. The registry may provide important information to understand symptom development of the neurodegenerative diseases, in which may help physicians to diagnose the diseases more accurately and provide better treatment plans.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age should be between 18-80 years old.

Disqualifiers

Patients with ongoing central nervous system infection and/or acute stroke or active brain tumor.

Trial population

Subjects will be recruited in neurology outpatient clinic in Prince of Wales Hospital, Hong Kong, who meet the inclusion and exclusion criteria listed above.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,400 Participants
are grouped into 9 trial groups

9

Trial groups

See each trial group below.

Group A: Early idiopathic Parkinson's Disease
Group B: Non-early idiopathic Parkinson's Disease
Group C: Multiple System Atrophy
Group D: Progressive Supranuclear Palsy
Group E: Alzheimer's Disease
Group F: Motor Neuron Disease
Group G: Small Vessel Disease
Group H: Frontotemporal Dementia
Group I: Healthy Control

Trial outcomes

Primary outcomes

1

the score change in Unified Parkinson's Disease Rating Scale (UPDRS)

The Unified Parkinson's Disease Rating Scale (UPDRS) would be administered to assess disease severity for iPD, PSP and SVD patients with parkinsonism features

Time frame
baseline visit, 2 years after baseline visit, 4 years after baseline visit
2

the score change in Unified MSA Rating Scale (UMSARS)

The Unified MSA Rating Scale (UMSARS) would be administered to assess disease severity for patients with MSA

Time frame
baseline visit, 2 years after baseline visit, 4 years after baseline visit
3

the score change in Montreal Cognitive Assessment Hong Kong version (HK-MoCA)

Montreal Cognitive Assessment Hong Kong version (HK-MoCA) is used to assess participants' cognitive functions for all groups

Time frame
baseline visit, 2 years after baseline visit, 4 years after baseline visit

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Vincent Mok

Lead sponsor

Chinese University of Hong Kong

Sponsor institution