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NCT05452993Completed

Screening for Diabetic Retinopathy in Pharmacies With Artificial Intelligence Enhanced Retinophotography

Acceptability and Efficiency of Screening for Diabetic Retinopathy in Pharmacies With Artificial Intelligence Enhanced Retinophotography : a French Pilot Study

Source: ClinicalTrials.gov · Last updated 25 Jul 2025

Brief summary (registry, in English)

Diabetic retinopathy is frequent, potentially severe with visual threat, health costly and represents a major public health problem. However, screening compliance for retinopathy remains too low in France, approximately 40% patients with diabetes laking diabetic retinopathy screening for at least 2 years. DIABeyeIA is a prospective pilot study evaluating the effectiveness and acceptability of diabetic retinopathy screening in 11 pharmacies in Normandy (north of France) using a non-mydriatic portable retinophotograph enhanced by artificial intelligence software. The main goal of this work is to evaluate a potential increase rate of diabetic retinopathy screening, compared to the actual rate (64% in France). Secondary goals are faisability, satisfaction and economical considerations for implementation of such a new screening program.

Status (registry)
Completed
Study type
Interventional
Enrollment
64 (actual)
First submitted
3 Jan 2022
Start date
16 Dec 2022
Primary completion date
5 Dec 2023
Lead sponsor
University Hospital, Caen
NCT number
NCT05452993

What you commit to

  • Study type: Interventional
  • Participants enrolled: 64
  • From 16 Dec 2022 to the primary completion date, 5 Dec 2023
  • 1 site in 1 country
  • 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

  • Patient unable to read, write or give consent
  • Patient refusing to share results with their general practitioner or ophthalmologist

Who the study is looking for

  • Adult patients with diabetes
  • Ongoing diabetes treatment (oral hypoglycaemic agents, injectable GLP-1 receptor agonists and insulin)
  • Regular customer of the pharmacy (at least 3 previous visits)
  • Informed consent to participate to the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Caen University Hospital
Coordinator of this site? Confirm its status
CaenFranceUnknown status

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