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NCT05740683Recruiting

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

Source: ClinicalTrials.gov · Last updated 2 Oct 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
13 Feb 2023
Start date
Feb 2023
Primary completion date
Dec 2032
Lead sponsor
Danish Dementia Research Centre
NCT number
NCT05740683

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From Feb 2023 to the primary completion date, Dec 2032
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Olfactory dysfunction with response to systemic or local corticosteroids if tried
  • Current alcohol or drug abuse
  • Current alcohol or drug abuse

Other illness

  • 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.
  • Severe nasal cavity abnormalities or infections.
  • Overt signs of dementia or PD
  • Terminal illness
  • Diagnosed with neurodegenerative disease or major neurological/psychiatric condition.
  • Overt signs of dementia or PD
  • Severe nasal cavity abnormalities or infections.
  • Diagnosed with neurodegenerative disease or major neurological/psychiatric condition.

Other

  • Olfactory dysfunction on clinical test

Who the study is looking for

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

Age in the registry: 55 years to 75 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Oskar McWilliam
Coordinator of this site? Confirm its status
CopenhagenDenmarkRecruiting
Danish Dementia Research Centre
Coordinator of this site? Confirm its status
CopenhagenDenmarkRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.