RT-QuiC
Diagnostic TestRT-QuIC measures the ability of aSyn to misfold other aSyn proteins and is an amplification technique.
NCT Number: NCT05740683
Test of early warning signs and RT-QuIC in patients with idiopathic olfactory dysfunction
Interested in participating?
Request Info55 year–75 year
All sexes
Observational
Danish Dementia Research Centre, Copenhagen, Denmark
Background. The number of persons living with dementia is increasing in Denmark and worldwide because the population is generally growing older. Dementia with Lewy bodies (DLB) is the second most prevalent etiology among the neurodegenerative diseases that give rise to dementia.
DLB is characterized by many prodromal symptoms years before dementia is evident. Currently, little is known about the course of symptoms in the prodromal phase, and furthermore, the diagnosis of DLB can be clinically challenging, especially in the early stages. DLB is like Parkinson's disease (PD), characterized by the accumulation of alpha-synuclein, which misfolds and aggregates within neurons in so-called Lewy Bodies; this assumably drives the neurodegeneration. A novel technique for the measurement of misfolded alpha-synuclein is Real-Time Quaking-Induced Conversion (RT-QuIC), which may be able to support the diagnostic process as well as aid in identifying patients with prodromal DLB. This would enable earlier symptomatic relief and care and potentially promote the search for disease-modifying therapies, which is currently absent.
Objectives. The overarching objective of this project is to identify early clinical warning signs and biomarkers in prodromal DLB.
Method. Study 1: Exploratory cross-sectional case-control study of patients with olfactory dysfunction versus individuals without olfactory dysfunction assessing pathological alpha-synuclein by RT-QuIC and prodromal symptoms of DLB and Parkinson's Disease.
Study 2: Longitudinal follow-up in Danish registries on diagnosing PD and dementia.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
with patients iOD:
Exclusion criteria
with patients iOD:
Inclusion criteria
controls:
Exclusion criteria
controls:
RT-QuIC measures the ability of aSyn to misfold other aSyn proteins and is an amplification technique.
Time frame: 24 months
Time frame: 8 years
A diagnosis of PD or dementia in national databases.
Time frame: 24 months
Sniffin Sticks identification test (SIT16)
Time frame: 24 months
Sniffin Sticks 48 (score 0-48)
Time frame: 24 months
Movement Disorder's Unified Parkinson's Rating Scale (MDS-UPDRS-III) (score 0-132)
Time frame: 24 months
Movement Disorder's Unified Parkinson's Rating Scale (MDS-UPDRS-I) (score 0-52)
Time frame: 24 months
Movement Disorder's Unified Parkinson's Rating Scale (MDS-UPDRS-II) (score 0-52)
Time frame: 24 months
MoCA, SDMT, Recall test and fluency (Animals/1 min)
Time frame: 24 months
MDS Prodromal PD probability
Time frame: Ever
REM Sleep Behavior Disorder Screening Questionnaire (RBDSQ) (score 0-13) and REM Sleep Behavior Disorder Single-Question Screen (RBD1Q)
Time frame: Now
The Farnsworth-Munsell 100 Hue Color Vision test (score 0-1000)
Time frame: 10 years
Co-morbidities and medication
Contact information is provided by the study sponsor or research team.
Kristian S Frederiksen
CONTACT
Oskar McWilliam
CONTACT
Danish Dementia Research Centre
Network
Acronym: AROMA
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.
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