Fact CheckerSign in

NCT04954183Completed

Development of an EEG Diagnostic for Alzheimer's Disease

Development of an EEG Diagnostic for Alzheimer's Disease: A Feasibility Study

Source: ClinicalTrials.gov · Last updated 25 Sept 2025

Brief summary (registry, in English)

The purpose of this research is to collect and compare electroencephalogram data from all stages of Alzheimer's disease from preclinical through severe dementia.

Status (registry)
Completed
Study type
Observational
Enrollment
29 (actual)
First submitted
29 Jun 2021
Start date
1 Oct 2021
Primary completion date
24 Jul 2025
Lead sponsor
Mayo Clinic
NCT number
NCT04954183

What you commit to

  • Study type: Observational
  • Participants enrolled: 29
  • From 1 Oct 2021 to the primary completion date, 24 Jul 2025
  • 1 site 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

  • Previous stroke.
  • Psychoactive drug use will be exclusionary in the prospectively obtained clinical patients.

Other illness

  • Any other potentially confounding neurologic illness (typically anything that causes structural brain damage).
  • Psychoactive medication use will not be an absolute exclusionary criterion in patients with moderate to severe dementia but patients who are relatively drug-free will be prioritized to the extent they are available within the study period.

Other

  • Severe head injury.
  • Craniotomy.

Who the study is looking for

  • 5 individuals with moderate to severe dementia, 5 with mild stage dementia, 5 with amnestic MCI, 5 presymptomatic APOE e4 carriers, and 5 age, sex, and education matched APOE e4 noncarriers. Additionally we will include a group of 5 patients with mild to moderate stage dementia with Lewy bodies (DLB), the second most common degenerative dementia, to explore differences from clinically typical Alzheimer's disease patients given the known clinical differences in EEG dysrhythmic severity between them (total of 30).
  • Unimpaired APOE e4/4 homozygotes age 65-75 and APOE e3/4 heterozygotes age 75-85 for the preclinical AD subset and age, sex, and education matched APOE e4 noncarriers for the unaffected controls.
  • Biomarker confirmation for preclinical diagnosis will be utilized to the extent possible (a subset of 130 members of our cohort have undergone amyloid-PET resulting in approximately 45 who are amyloid positive).

Age in the registry: 50 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Mayo Clinic in Arizona
Coordinator of this site? Confirm its status
ScottsdaleUnited StatesUnknown status

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