Fact CheckerSign in

NCT05698316Completed

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

A Collaborative Resource of Heidelberg Multimodal Imaging of Intermediate and Early Atrophic AMD Cases to Study Prediction of Disease Progression: (INTERCEPT-AMD)

Source: ClinicalTrials.gov · Last updated 8 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
1000 (actual)
First submitted
12 Jan 2023
Start date
4 May 2023
Primary completion date
22 Feb 2024
Lead sponsor
Association for Innovation and Biomedical Research on Light and Image
NCT number
NCT05698316

What you commit to

  • Study type: Observational
  • Participants enrolled: 1000
  • From 4 May 2023 to the primary completion date, 22 Feb 2024
  • 25 sites in 9 countries
  • 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.

Other illness

  • Co-existent ocular disease: Any other ocular condition that, in the investigator's opinion, might affect or alter visual acuity during the study.

Other

  • Both eyes have exudative AMD or geographic atrophy at baseline.
  • Any patient who has opted out of their information being used for research nationally or locally at any Member Site.

Who the study is looking for

  • Each dataset per patient should have one eye as the study eye with:
  • Intermediate AMD with no atrophy and no subretinal drusenoid deposits
  • Intermediate AMD with no atrophy with subretinal drusenoid deposits
  • Intermediate AMD with early atrophy (iRORA) with no Subretinal drusenoid deposits
  • Intermediate AMD with early atrophy (iRORA) with Subretinal drusenoid deposits
  • Intermediate AMD with evidence of cRORA
    • Non-study eye images will not be exported but information about the status of the macula should be added using the following options:
  • Established Geographic Atrophy (cRORA)
  • Exudative AMD (presence of MNV)
  • Early AMD
  • Healthy macula

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (25)

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

SiteCityCountrySite status
University Hospital Basel, University Eye Clinic, Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandUnknown status
Swiss Visio Retina Research Center, Swiss Visio Montchoisi
Coordinator of this site? Confirm its status
LausanneSwitzerlandUnknown status
Department of Ophthalmology University of Bonn
Coordinator of this site? Confirm its status
BonnGermanyUnknown status
Department of Ophthalmology, University of Freiburg
Coordinator of this site? Confirm its status
Freiburg im BreisgauGermanyUnknown status
Department of Ophthalmology Justus/Liebig/University/Giessen
Coordinator of this site? Confirm its status
GiesenGermanyUnknown status
Department of Ophthalmology University of Muenster Medical Center
Coordinator of this site? Confirm its status
MünsterGermanyUnknown status
Department of Ophthalmology St. Franziskus/Hospital Münster
Coordinator of this site? Confirm its status
MünsterGermanyUnknown status
Eye Clinic Sulzbach, Knappschaft Hospital Saar
Coordinator of this site? Confirm its status
SulzbachGermanyUnknown status
Institut Català de Retina (ICR), Clinical Trial Unit
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Valles Ophthalmology Research, S.L.
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Institut de la Màcula Centro Médico Teknon
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Clínica Oftalmológica AIKEN / Fundación Aiken de la Comunitat Valenciana
Coordinator of this site? Confirm its status
ValenciaSpainUnknown status
Department of Ophthalmology, University Hospital, Nantes
Coordinator of this site? Confirm its status
NantesFranceUnknown status
Clinical Trial Unit, Dep. Ophth., Gloucestershire Hospitals NHS Foundation Trust
Coordinator of this site? Confirm its status
CheltenhamUnited KingdomUnknown status
Clinical Eye Research Centre - St. Paul's Eye Unit, Royal Liverpool University Hospital
Coordinator of this site? Confirm its status
LiverpoolUnited KingdomUnknown status
NIHR Moorfields Clinical Research Facility, Moorfields Eye Hospital, NHS Foundation Trust
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status
Royal Victoria Eye and Ear Research Foundation
Coordinator of this site? Confirm its status
DublinIrelandUnknown status
Medical Retina Service, Operative Unit Ophthalmology / MultiMedica Spa (IRCCSMM)
Coordinator of this site? Confirm its status
MilanItalyUnknown status
Eye Unit, University Hospital Maggiore della Carità
Coordinator of this site? Confirm its status
NovaraItalyUnknown status
Department of Ophthalmology University of Udine
Coordinator of this site? Confirm its status
UdineItalyUnknown status
Department of Ophthalmology Radboud University Medical Centre Nijmegen
Coordinator of this site? Confirm its status
NijmegenNetherlandsUnknown status
AIBILI-CEC (AIBILI- Clinical Trials Centre)
Coordinator of this site? Confirm its status
CoimbraPortugalUnknown status
Espaço Médico de Coimbra
Coordinator of this site? Confirm its status
CoimbraPortugalUnknown status
Instituto de Oftalmologia Dr. Gama Pinto
Coordinator of this site? Confirm its status
LisbonPortugalUnknown status
Department of Ophthalmology Porto Medical School / Hospital S. João
Coordinator of this site? Confirm its status
PortoPortugalUnknown status

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