Optimization and Evaluation of the Diagnosis and Treatment System for Diabetic Retinopathy in Type 2 Diabetes Mellitus
Condition(s) studied
Investigational drug(s) / intervention(s)
Fundus Examination: Performing fundus photography on patients to assess the progression of diabetic retinopathy (DR).
Metabolomics analysis: Conduct metabolomics testing at enrollment.
Study summary
This study aims to integrate clinical indicators and features of fundus images, combined with metabolomics, to construct an early warning model for diabetic retinopathy (DR) in type 2 diabetes. By combining clinical indicators with metabolomics, the investigators aim to establish a precise DR typing model based on the age of diabetes onset (early-onset diabetes, late-onset diabetes) and based on the coexistence with two types of diabetic macrovascular complications. A multidisciplinary collaboration will be conducted for comprehensive management of DR to control the progression of moderate-stage DR. Cloud-based patient rooms combined with continuous glucose monitoring (CGM) will further explore the role of integrated diabetes retinopathy ward management models in the management of patients undergoing diabetes retinopathy surgery, pioneering a new model for the management of advanced DR.
Eligibility
Primary outcome measure(s)
- Fundus examination — Conduct examinations at enrollment and twelve months after enrollment.
Assess the severity of diabetic retinopathy (DR), and group accordingly. The high - risk DR cohort and the early - stage DR cohort have a fundus examination once a year; the mid - stage DR cohort has a fundus examination every six months; the late - stage DR cohort has a fundus examination every three months.
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| The first hosptial of lanzhou university | Lanzhou | China | Recruiting |
| Shanghai general hosptial | Shanghai | China | Recruiting |
| The forth people's hosptial of shenyang | Shenyang | China | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06821399 on ClinicalTrials.gov ↗ ← All trials in China