Actively Recruiting

Age: 55Years +
All Genders
Healthy Volunteers
NCT03761381

OCT Angiography and NRAI in Dementia

Led by Oregon Health and Science University · Updated on 2025-09-12

20

Participants Needed

1

Research Sites

480 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary goals of this study are to use optical coherence tomography (OCT) angiography (blood vessel mapping) to: 1. Detect retinal blood vessel and blood flow changes in participants with dementia. 2. Detect amyloid protein deposits in the retinas of participants with dementia.

CONDITIONS

Official Title

OCT Angiography and NRAI in Dementia

Who Can Participate

Age: 55Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Physician-confirmed diagnosis of probable Alzheimer's disease (for dementia subjects)
  • Mild dementia defined by Mini-Mental State Exam score of 20 or greater, or Montreal Cognitive Assessment score of 15 or greater, or Clinical Dementia Rating Scale score of 1 (for dementia subjects)
  • Age older than 55 years
  • Ability to comply with study procedures
  • Corrected visual acuity of at least 20/400 in either eye (for dementia subjects)
  • Has a legally authorized representative to sign consent and accompany participant (for dementia subjects)
  • Able to maintain stable fixation for OCT imaging (for dementia-free controls)
  • Corrected visual acuity of at least 20/40 in either eye (for dementia-free controls)
  • Dementia-free defined by Mini-Mental Status Exam score of 24 or greater, or Montreal Cognitive Assessment score of 18 or greater, or Clinical Dementia Rating less than 1.0 (for dementia-free controls)
Not Eligible

You will not qualify if you...

  • Non-Alzheimer's primary neurological diseases affecting the central nervous system (e.g., multiple sclerosis, Parkinson's disease)
  • Ocular diseases or pathology within last year that interfere with dementia assessment (e.g., glaucoma, diabetic or hypertensive retinal disease, amblyopia)
  • Media opacity such as cataract, corneal scar, or vitreous opacity interfering with retinal imaging
  • Previous intraocular surgery except uncomplicated cataract extraction with lens implantation
  • Inability to maintain stable fixation for OCT imaging or provide informed consent
  • Refractive error greater than +3 or less than -7 diopters, or astigmatism greater than 2 diopters
  • Diabetes longer than 10 years or hemoglobin A1C above 10 within 180 days before OCT scan
  • Uncontrolled hypertension with systolic BP above 170 or diastolic BP above 100
  • Arrhythmia with irregular pulse or heart rate outside 50-110 beats per minute
  • Pregnancy or breastfeeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Oregon Health & Science University

Portland, Oregon, United States, 97239

Actively Recruiting

Loading map...

Research Team

D

Denzil Romfh, OD

CONTACT

H

Humberto Martinez, COT

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

OCT Angiography and NRAI in Dementia | DecenTrialz