Actively Recruiting

All Genders
NCT06400368

Effect of LEQEMBI on Cerebral and Retinal Amyloid in Mild Cognitive Impairment Due to Alzheimer's Disease

Led by NeuroVision Imaging · Updated on 2024-05-07

200

Participants Needed

1

Research Sites

101 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a proof of concept observational study is to determine if there is correlation between Aβ plaques and vascular findings in the Retina versus brain ARIA.

CONDITIONS

Official Title

Effect of LEQEMBI on Cerebral and Retinal Amyloid in Mild Cognitive Impairment Due to Alzheimer's Disease

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be 50 years old or older
  • Must be eligible for and intend to receive LEQEMBI as standard care treatment
  • Must be willing to comply with the study protocol including pupil dilation to at least 3.5 mm for eye imaging
  • Patient or legally authorized representative must understand the study purpose and risks and provide informed consent
Not Eligible

You will not qualify if you...

  • History of acute angle-closure glaucoma or allergic reaction to pupil dilation medication
  • Presence of dense cataracts or other significant eye media opacity affecting retinal imaging
  • Eye surgery within the past 2 months or current use of eye drops related to recent eye surgery
  • Unable or unwilling to comply with study protocol requirements

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sutter Health

Sacramento, California, United States, 95816

Actively Recruiting

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Research Team

M

Mieko Chambers, MS

CONTACT

J

Josef Tamory

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

0

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