UZ Leuven
Leuven, 3000, Belgium
Location status: Recruiting
NCT Number: NCT06875765
AIM: To investigate whether SV2A loss spreads from brainstem to cerebral cortex with progression of Parkinson's disease (PD) and to determine whether longitudinal cortical SV2A loss correlates with cognitive decline in PD.
STUDY DESIGN: The investigators will re-invite participants (both patients with PD and healthy controls) of a previous longitudinal study (NCT04243304, S61477) to undergo evaluation approximately 7 years after the initial baseline study visit (i.e. on average 10 years since the first motor symptoms). All participants will undergo clinical assessment of motor and non-motor symptoms (including cognitive testing), as well as 11C-UCB-J PET-CT (targeting synaptic density marker SV2A), 18F-FE-PE2I PET-CT (targeting DAT) and brain MRI.
Interested in participating?
Request Info30 year and older
All sexes
Interventional
Not applicable
Leuven, 3000, Belgium
Location status: Recruiting
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Positron Emission Tomography (PET) of synaptic vesicle protein 2A (SV2A) using the radioligand 11C-UCB-J.
Positron Emission Tomography (PET) of dopamine transporter (DAT) using the radioligand 18F-FE-PE2I.
Magnetic resonance imaging of brain volume.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Cross-sectional differences (%) in SV2A signal at Year 7 between Parkinson disease patients and controls.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Cross-sectional correlation between clinical scores and SV2A in Parkinson disease patients at Year 7.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Differences (%) in the rate of SV2A change between baseline and Year 7 between Parkinson disease patients and controls.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Correlation between progression of the clinical scores and longitudinal SV2A changes in Parkinson disease patients.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Cross-sectional differences (%) in DAT levels at Year 7 between Parkinson disease patients and controls.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Cross-sectional correlation between clinical scores and DAT levels in Parkinson disease patients at Year 7.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Differences (%) in the rate of DAT level change between baseline and Year 7 between Parkinson disease patients and controls.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Correlation between progression of the clinical scores and longitudinal DAT level changes in Parkinson disease patients.
Time frame: Data analysis will be done when all subjects have undergone Year 7 evaluation.
Correlation between SV2A changes and DAT level changes in Parkinson disease patients.
Interested in participating?
Request InfoUniversitaire Ziekenhuizen KU Leuven
Other
Longitudinal Measurement of Synaptic Loss and Cognitive Decline in the Long-term Course of Parkinson's Disease
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06466525
Basal Ganglia Diseases, Brain Diseases
Melbourne, Victoria, Australia
View Trial DetailsNCT07838636
Basal Ganglia Diseases, Brain Diseases
Warsaw, Poland
View Trial DetailsNCT07005180
Basal Ganglia Diseases, Brain Diseases
Farmington Hills, Michigan, United States
View Trial DetailsNCT07056361
Basal Ganglia Diseases, Brain Diseases
Pittsburgh, Pennsylvania, United States
View Trial Details