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
- Diseases
- Macular degeneration
- 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
Sites (25)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital Basel, University Eye Clinic, Basel Coordinator of this site? Confirm its status | Basel | Switzerland | Unknown status |
| Swiss Visio Retina Research Center, Swiss Visio Montchoisi Coordinator of this site? Confirm its status | Lausanne | Switzerland | Unknown status |
| Department of Ophthalmology University of Bonn Coordinator of this site? Confirm its status | Bonn | Germany | Unknown status |
| Department of Ophthalmology, University of Freiburg Coordinator of this site? Confirm its status | Freiburg im Breisgau | Germany | Unknown status |
| Department of Ophthalmology Justus/Liebig/University/Giessen Coordinator of this site? Confirm its status | Giesen | Germany | Unknown status |
| Department of Ophthalmology University of Muenster Medical Center Coordinator of this site? Confirm its status | Münster | Germany | Unknown status |
| Department of Ophthalmology St. Franziskus/Hospital Münster Coordinator of this site? Confirm its status | Münster | Germany | Unknown status |
| Eye Clinic Sulzbach, Knappschaft Hospital Saar Coordinator of this site? Confirm its status | Sulzbach | Germany | Unknown status |
| Institut Català de Retina (ICR), Clinical Trial Unit Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Valles Ophthalmology Research, S.L. Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Institut de la Màcula Centro Médico Teknon Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Clínica Oftalmológica AIKEN / Fundación Aiken de la Comunitat Valenciana Coordinator of this site? Confirm its status | Valencia | Spain | Unknown status |
| Department of Ophthalmology, University Hospital, Nantes Coordinator of this site? Confirm its status | Nantes | France | Unknown status |
| Clinical Trial Unit, Dep. Ophth., Gloucestershire Hospitals NHS Foundation Trust Coordinator of this site? Confirm its status | Cheltenham | United Kingdom | Unknown status |
| Clinical Eye Research Centre - St. Paul's Eye Unit, Royal Liverpool University Hospital Coordinator of this site? Confirm its status | Liverpool | United Kingdom | Unknown status |
| NIHR Moorfields Clinical Research Facility, Moorfields Eye Hospital, NHS Foundation Trust Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| Royal Victoria Eye and Ear Research Foundation Coordinator of this site? Confirm its status | Dublin | Ireland | Unknown status |
| Medical Retina Service, Operative Unit Ophthalmology / MultiMedica Spa (IRCCSMM) Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| Eye Unit, University Hospital Maggiore della Carità Coordinator of this site? Confirm its status | Novara | Italy | Unknown status |
| Department of Ophthalmology University of Udine Coordinator of this site? Confirm its status | Udine | Italy | Unknown status |
| Department of Ophthalmology Radboud University Medical Centre Nijmegen Coordinator of this site? Confirm its status | Nijmegen | Netherlands | Unknown status |
| AIBILI-CEC (AIBILI- Clinical Trials Centre) Coordinator of this site? Confirm its status | Coimbra | Portugal | Unknown status |
| Espaço Médico de Coimbra Coordinator of this site? Confirm its status | Coimbra | Portugal | Unknown status |
| Instituto de Oftalmologia Dr. Gama Pinto Coordinator of this site? Confirm its status | Lisbon | Portugal | Unknown status |
| Department of Ophthalmology Porto Medical School / Hospital S. João Coordinator of this site? Confirm its status | Porto | Portugal | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.