Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Using advanced eye imaging to study memory impairment

Official title: OCT-Angiography and Adaptive Optics in Patients With Memory Impairment

Run by Fondation Ophtalmologique Adolphe de Rothschild · NCT04389437 · Data updated 2026-11-12

This study is trying to see if new eye imaging techniques can help find changes in the retina that might be linked to memory problems like Alzheimer's and other types of dementia.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment450 (estimated)
SponsorFondation Ophtalmologique Adolphe de Rothschild
Research network
Locations1 site (Paris)
StatusRecruiting
StartedJune 26, 2020
Main results expectedJune 2027
Study endsJune 2027
Registry record updatedOctober 30, 2026
Trial IDNCT04389437 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals presenting with memory complaints or those accompanying such patients.

Probably not a fit

Patients with significant retinal pathology or severe cognitive impairment may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the relationship between retinal abnormalities and neurocognitive disorders (NCD) such as Alzheimer's disease and other forms of dementia. It employs two innovative ophthalmological imaging techniques, Optical Coherence Tomography Angiography (OCT-A) and Adaptive Optics (AO), to non-invasively analyze the morphology of small retinal vessels and the overall architecture of the retina. By comparing these parameters, the study aims to identify specific retinal anomalies associated with various NCDs, potentially serving as in vivo markers of the underlying pathophysiological processes. This pilot study is the first of its kind to explore these techniques in the context of memory impairment.

Why it matters

Potential benefit: If successful, this study could lead to new diagnostic markers for early detection of neurocognitive disorders.

How similar studies have gone: While this approach is novel and has not been tested in this specific context, similar studies have shown promise in linking retinal health to neurodegenerative conditions.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient presenting in memory consultation for memory complaint or person accompanying a patient in memory consultation for memory complaint

Exclusion Criteria:

* pregnant or lactating women
* history of known non-degenerative neurological pathology (tumor, stroke territorial, in particular multiple sclerosis)
* history of retinal pathology
* ametropia greater in absolute value than 3 diopters on the sphere, or/and 1.5 diopters on the cylinder.
* history of taking ethambutol for more than 2 months
* history of takingsynthetic antimalarial for more than 2 years
* Mini Mental State Score (MMS) and / or Montreal Cognitive Assessment (MoCA) \<10 for patients and 26 for accompanying persons
* MRI contraindication (for patients only)

Where it's running

  • Hôpital Fondation A. de Rothschild
    Paris, France
    Recruiting

Study contacts

  • Principal investigator: Antoine MOULIGNIER, MD — Fondation A. de Rothschild
  • Study coordinator: Amélie YACHITZ, MD
  • Email: ayavchitz@for.paris
  • Phone: (0)148036454

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.