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Longitudinal ultra-high field imaging in Parkinson’s Disease: Tracking the disease course.

Longitudinal ultra-high field imaging in Parkinson’s Disease: Tracking the disease course.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON23958
Enrollment
190
Registered
2019-03-05
Start date
2019-06-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Parkinson's Disease

Interventions

None listed

Sponsors

In this project we work together with patients and their representatives, MHeNs School for Mental Health and Neuroscience, Maastricht University Medical Centre (MUMC+), BioBank Maastricht UMC+ and Scannexus.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants are eligible for participation in this study if they meet the following criteria: 1) All patients have to be diagnosed with PD by a neurologist, within the last 3 years before inclusion. 2) A score of = 24 on the Montreal Cognitive Assessment (MoCA) at baseline. 3) Able to read and understand Dutch. 4) 18 years of age or older. 5) Providing written informed consent.

Exclusion criteria

Exclusion criteria: 1) Subjects with contra-indications for a MRI scan, such as claustrophobia or subjects carrying incompatible metallic devices such as pacemakers and certain mechanical valves. 2) Advanced cognitive impairment (MoCA <24) or dementia according to the DSM V criteria at baseline. 3) Subjects with other neurodegenerative diseases.

Design outcomes

Primary

MeasureTime frame
-To determine early and subtle MRI changes in PD patients which distinguish them from the healthy population and to create a diagnostic tool for neurologists based on these differences.

Secondary

MeasureTime frame
- To detect whether different clinical phenotypes of PD patients also show different imaging characteristics. - To correlate MRI characteristics to clinical phenotype, genetic characteristics and progression of symptoms and thereby providing a prognostic tool for individual PD patients.

Contacts

Public ContactAmée Wolters

Maastricht University Medical Centre+

amee.wolters@mumc.nl+31620474976

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)