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NCT05698316: INTERCEPT-AMD

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

Active, enrolled Last updated 30 September 2025
What this trial tests

trial testing Collection of both retrospective and prospective data collection in 3 visits. in Age Related Macular Degeneration in 1,000 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
4 May 2023
Primary endpoint
22 February 2024
31 December 2025

Quick facts

Lead sponsorAssociation for Innovation and Biomedical Research on Light and Image
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment1,000
Start date4 May 2023
Primary completion22 February 2024
Estimated completion31 December 2025
Sites25 locations across France, Italy, Netherlands, Ireland, United Kingdom, Germany, Switzerland, Portugal

Drugs / interventions tested

Conditions studied

Sponsor

Association for Innovation and Biomedical Research on Light and Image

Who can join

Eligibility, any sex, with Age Related Macular Degeneration or Intermediate AMD. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Human retinal secretome: A cross-link between mesenchymal and retinal cells.
    Donato L, Scimone C, Alibrandi S, Scalinci SZ, et al · · 2023 · cited 6× · PMID 37545752 · DOI 10.4252/wjsc.v15.i7.665

Verify or expand the search:

Other recruiting trials for Age Related Macular Degeneration

Currently open trials in the same condition.

Other Association for Innovation and Biomedical Research on Light and Image trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05698316.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing