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NCT07149142Recruiting

Pediatric Artificial Intelligence for Retinopathy Screening in Children With Type 1 Diabetes

Feasibility and Effectiveness of Diabetic Retinopathy Screening Using Artificial Intelligence in Children With Type 1 Diabetes

Source: ClinicalTrials.gov · Last updated 20 Jul 2026

Brief summary (registry, in English)

The proposed project is a clinical intervention trial testing the feasibility and effectiveness of diabetic retinopathy screening evaluated by artificial intelligence (AI) based software in children with type 1 diabetes (CwD). Another novel method, the confocal microscopy of the retina will be used to assess the early stages of diabetic neuropathy. In parallel, we aim to assess the prevalence of diabetic retinopathy and neuropathy in a well-controlled population of CwD at a tertiary diabetes care center. Each participant will undergo an examination of diabetic retinopathy using the non-mydriatic fundus camera. The resulting photography will be evaluated by AI driven software. The participant will then follow this examinaton with fundus ophtalmoscopy in arteficial mydriasis as a standard method of diabetic retinopathy assessment. Another method, the optic coherence tomography (OCT), which is considered as the most sensitive method for diabetic retinopathy assessment, will be performed after that. The results of these methods will be compared to assess the sensitivity of each. The examination-satisfaction questionnaire will be given to the participants. In subjects over 18 years, a confocal microscopy of the retina examination will be performed to assess the status of the corneal sub-basal nerve plexus and the presence of diabetic neuropathy will be noted. The prevalence of diabetic retinopathy and neuropathy in this group of children with diabetes will be assessed based on the results.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
400 (estimated)
First submitted
14 Aug 2025
Start date
1 Jul 2026
Primary completion date
31 Dec 2027
Lead sponsor
University Hospital, Motol
NCT number
NCT07149142

What you commit to

  • Study type: Interventional
  • Planned participants: 400
  • From 1 Jul 2026 to the primary completion date, 31 Dec 2027
  • 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

  • Unwillingness to sign a written informed consent by both the CwD and their parent/caregiver

Who the study is looking for

  • Type 1 diabetes diagnosed according to the ADA criteria
  • Age over 11.0 years or duration of diabetes over 2 years
  • Signed written informed consent by both the CwD and their parent/caregiver

Age in the registry: 11 years to 19 years · 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
University Hospital Motol
Coordinator of this site? Confirm its status
PragueCzechiaRecruiting

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