Parkinson's Repository of Biosamples and Network Datasets (Tracking Parkinson's)

NCT ID: NCT02881099

Last Updated: 2024-11-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

2614 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-11-13

Study Completion Date

2022-12-31

Brief Summary

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Prospective observational study of Parkinson's disease with repeat clinical assessment and biobanking of blood samples.

Detailed Description

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To identify genetic and biomarker factors which affect the expression of Parkinson's Disease.

Primary objective: To define the severity and rates of progression of clinical features of Parkinson's Disease.

Secondary objective: To relate clinical phenomenology of Parkinson's disease to genetic and biomarker changes.

Conditions

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Parkinson's Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Recent diagnosis (P3)

Primary cohort; participants recruited if diagnosed within the last three years

No interventions assigned to this group

Early diagnosis (P50)

Participants recruited if diagnosed before the age of 50 years old

No interventions assigned to this group

Relatives (R)

Siblings of existing participants

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Diagnosis of Parkinson's disease, based on UK Brain Bank criteria and made within the preceding 3 years ('recent onset cases') or diagnosed at under 50 years ('under 50 years cases')
2. Age ≥18 to \<90years
3. Subject is able and willing to provided informed consent.


1. Age ≥18 to \< 90years
2. Resident in the United Kingdom and able to access one of the PRoBaND study centres.
3. Subject is able and willing to provided informed consent.

Exclusion Criteria

1. Patient has severe comorbid illness that would prevent full study participation
2. Patient has features indicating another type of degenerative parkinsonism, e.g. progressive supranuclear palsy
3. Drug-induced parkinsonism (Drug-unmasked PD is allowed)
4. Symmetrical lower body parkinsonism attributable to significant cortical and/or subcortical cerebrovascular disease (patients with 'incidental' small vessel disease on brain imaging are allowed).
5. Negative or normal functional imaging of the presynaptic dopamine system


1. Subject has severe comorbid illness that would prevent study participation
2. Subject already has a diagnosis of Parkinson's disease
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Parkinson's UK

OTHER

Sponsor Role collaborator

University of Bristol

OTHER

Sponsor Role collaborator

Cardiff University

OTHER

Sponsor Role collaborator

University of Glasgow

OTHER

Sponsor Role collaborator

South Glasgow University Hospitals NHS Trust

OTHER

Sponsor Role lead

Responsible Party

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Dr Donald Grosset

Senior Research Fellow

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Donald Grosset, BSc, MD

Role: STUDY_DIRECTOR

University of Glasgow

References

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Malek N, Weil RS, Bresner C, Lawton MA, Grosset KA, Tan M, Bajaj N, Barker RA, Burn DJ, Foltynie T, Hardy J, Wood NW, Ben-Shlomo Y, Williams NW, Grosset DG, Morris HR; PRoBaND clinical consortium. Features of GBA-associated Parkinson's disease at presentation in the UK Tracking Parkinson's study. J Neurol Neurosurg Psychiatry. 2018 Jul;89(7):702-709. doi: 10.1136/jnnp-2017-317348. Epub 2018 Jan 29.

Reference Type DERIVED
PMID: 29378790 (View on PubMed)

Swallow DM, Lawton MA, Grosset KA, Malek N, Klein J, Baig F, Ruffmann C, Bajaj NP, Barker RA, Ben-Shlomo Y, Burn DJ, Foltynie T, Morris HR, Williams N, Wood NW, Hu MT, Grosset DG. Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts. J Neurol Neurosurg Psychiatry. 2016 Nov;87(11):1183-1190. doi: 10.1136/jnnp-2016-313642. Epub 2016 Sep 26.

Reference Type DERIVED
PMID: 27671901 (View on PubMed)

Other Identifiers

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GN11NE062

Identifier Type: -

Identifier Source: org_study_id