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NCT07828821Not yet recruiting

Screening for Diabetic RETINopathy Using a Non-mydriatic Retinograph Funduscope in Occupational MEDicine

Source: ClinicalTrials.gov · Last updated 18 Sept 2026

Brief summary (registry, in English)

Diabetic retinopathy is a complication of diabetes that can affect vision. Early detection and appropriate management can help prevent or delay vision loss. However, some people with diabetes do not receive the recommended regular eye examinations. The RETINOMED study is a pilot study designed to evaluate the feasibility of offering diabetic retinopathy screening to workers with diabetes through an Occupational Health service. Participants will attend a single study visit at the Occupational Health Department of Clermont-Ferrand University Hospital. During this visit, retinal photographs will be taken using a non-mydriatic retinal camera, which does not require pupil dilation. Participants will also complete a questionnaire about their sociodemographic and occupational characteristics, lifestyle, and diabetes. The study will assess the acceptability of this screening program among eligible workers. It will also estimate the prevalence of diabetic retinopathy among screened workers and explore participant characteristics that may be associated with diabetic retinopathy.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
400 (estimated)
First submitted
8 Sept 2026
Start date
Oct 2026
Primary completion date
Jun 2029
Lead sponsor
University Hospital, Clermont-Ferrand
NCT number
NCT07828821

What you commit to

  • Study type: Interventional
  • Planned participants: 400
  • From Oct 2026 to the primary completion date, Jun 2029
  • 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

  • Protected persons (minors, guardianship, curatorship, deprived of freedoms, safeguard of justice)
  • Pregnant or breastfeeding women; these women may be offered participation after pregnancy and/or breastfeeding
  • Non-voluntary person

Who the study is looking for

  • Worker
  • Adult (≥18 years old)
  • Diabetic
  • Affiliated with a Social Security scheme
  • Able to give informed consent to participate in the research

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. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Clermont-Ferrand
Coordinator of this site? Confirm its status
Clermont-FerrandFranceUnknown status

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