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Association of serum uric acid and its related metabolites with diabetic retinopathy

Association of serum uric acid and its related metabolites with diabetic retinopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094951
Enrollment
Unknown
Registered
2024-12-31
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic retinopathy

Interventions

Observation group:None

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with confirmed diabetes mellitus: meet internationally recognized diagnostic criteria for diabetes (such as those of the World Health Organization (WHO) or the American Diabetic Association (ADA)). Including people with type 1 diabetes and type 2 diabetes. 2. Age>=18 years. 3. The subjects can understand the purpose of the study, agree to complete the relevant examinations and collect biochemical, glycosylated hemoglobin eggs, C-reactive protein, erythrocyte sedimentation rate, renin + angiotensin + aldosterone data, ophthalmic imaging examinations including fundus photography, OCT results, and voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with other serious systemic diseases, such as advanced renal failure (eGFR <30 mL/min/1.73 m²), liver failure, heart failure and other serious systemic diseases, which may have a confounding effect on the research data. 2. Patients with other ophthalmic diseases: such as retinal vein occlusion, age-related macular degeneration, retinal detachment or other serious ophthalmic diseases that may interfere with the evaluation of diabetic retinopathy; 3. Pregnant or lactating women: Pregnant or lactating women are not suitable for inclusion in the study because physiological changes may affect the level of blood uric acid and metabolites. 4. Patients with acute inflammation or infection: Subjects have obvious acute inflammation or infection at screening, which may affect blood biochemical indicators. 5. Patients with severe mental illness or cognitive dysfunction: If the subject suffers from severe mental illness or cognitive dysfunction, it is difficult for the subject to cooperate with the study and follow-up work. 6. Subjects participating in other interventional clinical trials to avoid mutual interference between trials.

Design outcomes

Primary

MeasureTime frame
Classification of diabetic retinopathy;serum uric acid;

Secondary

MeasureTime frame
Macular retinal thickness;Indexes related to uric acid metabolism;Indexes related to plasma glucose;Indexes related to inflammation;

Countries

China

Contacts

Public ContactLiu Kun

Shanghai General Hospital

drliukun@sjtu.edu.cn+86 21 63240090

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026