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NCT Number: NCT05740683

Alpha-synuclein Rt-quic and Neurologic Symptoms in Persons With idiOpathic anosMiA

Test of early warning signs and RT-QuIC in patients with idiopathic olfactory dysfunction

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Key information

Age range

55 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Danish Dementia Research Centre, Copenhagen, Denmark

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About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

with patients iOD:

  • Age 55 -75 years of age
  • Slowly progressing and non-fluctuating iOD
  • Able to give informed consent and to cooperate as evaluated by the PI

Exclusion criteria

with patients iOD:

  • Diagnosed with a neurodegenerative disease or major neurological/psychiatric condition.
  • Anosmia/hyposmia caused by sino-nasal disease (including chronic rhinitis and allergy), after trauma, infection, congenial, olfactory dysfunction due to surgery, or toxins/drugs affecting the olfactory function.
  • Olfactory dysfunction with response to systemic or local corticosteroids if tried
  • Severe nasal cavity abnormalities or infections.
  • Overt signs of dementia or PD
  • Current alcohol or drug abuse
  • Terminal illness
  • Diagnosed with neurodegenerative disease or major neurological/psychiatric condition.

Inclusion criteria

controls:

  • Age 55 -75 years of age
  • Able to give informed consent
  • Able to cooperate as evaluated by the PI

Exclusion criteria

controls:

  • Olfactory dysfunction on clinical test
  • Overt signs of dementia or PD
  • Severe nasal cavity abnormalities or infections.
  • Current alcohol or drug abuse
  • Diagnosed with neurodegenerative disease or major neurological/psychiatric condition.

Treatment and study plan

RT-QuiC

Diagnostic Test

RT-QuIC measures the ability of aSyn to misfold other aSyn proteins and is an amplification technique.

Primary outcomes

  1. Real-time quaking-induced conversion (RT-QuIC) positive for alpha-synuclein (aSyn)

    Time frame: 24 months

  2. Diagnosis of Parkinson's disease (PD) or dementia

    Time frame: 8 years

    A diagnosis of PD or dementia in national databases.

Secondary outcomes

  1. Smell test

    Time frame: 24 months

    Sniffin Sticks identification test (SIT16)

  2. Smell test

    Time frame: 24 months

    Sniffin Sticks 48 (score 0-48)

  3. Motor function

    Time frame: 24 months

    Movement Disorder's Unified Parkinson's Rating Scale (MDS-UPDRS-III) (score 0-132)

  4. Dysautonomia and non-motor symptoms

    Time frame: 24 months

    Movement Disorder's Unified Parkinson's Rating Scale (MDS-UPDRS-I) (score 0-52)

  5. Subjective motor symptoms

    Time frame: 24 months

    Movement Disorder's Unified Parkinson's Rating Scale (MDS-UPDRS-II) (score 0-52)

  6. Cognition

    Time frame: 24 months

    MoCA, SDMT, Recall test and fluency (Animals/1 min)

  7. Prodromal PD

    Time frame: 24 months

    MDS Prodromal PD probability

  8. REM-sleep

    Time frame: Ever

    REM Sleep Behavior Disorder Screening Questionnaire (RBDSQ) (score 0-13) and REM Sleep Behavior Disorder Single-Question Screen (RBD1Q)

  9. Color vision

    Time frame: Now

    The Farnsworth-Munsell 100 Hue Color Vision test (score 0-1000)

  10. Co-morbidities and medication

    Time frame: 10 years

    Co-morbidities and medication

Study contacts

Contact information is provided by the study sponsor or research team.

Kristian S Frederiksen

CONTACT

[email protected]

Oskar McWilliam

CONTACT

[email protected]

+4535458759

Sponsors and collaborators

Lead sponsor

Danish Dementia Research Centre

Network

Collaborators

  • Danish Reference Center for Prion Diseases, Rigshospitalet
  • Department of Otorhinolaryngology, Head and Neck Surgery & Audiology, Rigshospitalet

Registry information

Acronym: AROMA

Important dates

Study start
2023
Primary completion
2032
Study completion
2032
First posted
Feb 23, 2023
Registry last updated
Oct 2, 2024

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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