EichorEICHOR
Study identifier: NCT05698316 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

A Collaborative Resource of Heidelberg Multimodal Imaging of Intermediate and Early Atrophic AMD Cases to Study Prediction of Disease Progression

Condition: Age Related Macular Degeneration · Intermediate AMD · Atrophy  ·  Sponsor: Association for Innovation and Biomedical Research on Light and Image

PhaseN/A
Planned participants1000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This is a multicentre retrospective and prospective cohort study with the goal to develop a well-characterised multimodal image database of eyes with intermediate AMD with and without early atrophy. The main objectives are: 1. Develop a collaborative well-characterised database on intermediate AMD with or without early atrophy. 2. Grading of these images to explore imaging markers of progression. 3. Develop predictive models as a secondary analysis of our dataset. This study will recruit around 1.000 eyes in 6 months. All consenting patients who have had at least 3 clinic visits with multimodal imaging done at least at 6 months interval between 2 visits and meet the inclusion and exclusion criteria will be included in the study for retrospective data collection. Those with one visit remaining to complete 2 years, images will be acquired prospectively. In addition to the images, routine demographic data (age and sex) and available visual acuity (VA) (BCVA if possible, VA with Pinhole or VA with patient's glasses) will be collected. Multimodal imaging includes mandated macular OCT with or without enhanced depth imaging and infrared imaging. Fundus autofluorescence (AF) and multicolor imaging are optional. All imaging must be done on Heidelberg Spectralis system.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (25)

Department of Ophthalmology, University Hospital, NantesNantes, France
Department of Ophthalmology University of BonnBonn, Germany
Department of Ophthalmology University of FreiburgFreiburg im Breisgau, Germany
Department of Ophthalmology Justus/Liebig/University/GiessenGiesen, Germany
Department of Ophthalmology St. Franziskus/Hospital MünsterMünster, Germany
Department of Ophthalmology University of Muenster Medical CenterMünster, Germany
Eye Clinic Sulzbach, Knappschaft Hospital SaarSulzbach, Germany
Royal Victoria Eye and Ear Research FoundationDublin, Ireland
Medical Retina Service, Operative Unit Ophthalmology / MultiMedica Spa (IRCCSMM)Milan, Italy
Eye Unit, University Hospital Maggiore della CaritàNovara, Italy
Department of Ophthalmology University of UdineUdine, Italy
Department of Ophthalmology Radboud University Medical Centre NijmegenNijmegen, Netherlands

+ 13 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.

Look up another condition
Look up another city
Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →