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Multimodal Imaging–Based Prediction of Anti-VEGF Treatment Response in Diabetic Macular Edema and Implications for Follow-up Strategies

Multimodal Imaging–Based Prediction of Anti-VEGF Treatment Response in Diabetic Macular Edema and Implications for Follow-up Strategies

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119836
Enrollment
Unknown
Registered
2026-03-04
Start date
2026-03-12
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Diabetic macular edema

Interventions

Observation group:None

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Participants were aged =18 years. 2.Participants had a confirmed diagnosis of diabetes mellitus and met the diagnostic criteria for diabetic macular edema (DME). 3.Participants received intravitreal anti–vascular endothelial growth factor (anti-VEGF) therapy using a 3-loading-dose plus pro re nata (3+PRN) regimen. 4.Participants completed 12 months of follow-up with key clinical data and OCT images available at baseline and throughout follow-up.

Exclusion criteria

Exclusion criteria: 1.Patients with a clinical diagnosis of retinal neovascularization or neovascular glaucoma were excluded. 2.Patients with other fundus disorders that could cause macular edema or alter macular structure—such as age-related macular degeneration (AMD), retinal vein occlusion (RVO), uveitis, epiretinal membrane, or vitreomacular traction syndrome—were excluded; patients with proliferative diabetic retinopathy requiring surgical intervention (e.g., vitreous hemorrhage or tractional retinal detachment) were also excluded. 3.Patients with severe systemic or anterior segment conditions affecting vision or OCT image quality—such as uncontrolled hypertension, nephrotic syndrome–related macular edema, advanced cataract, corneal opacity, dense vitreous opacity, or any other factor that could interfere with OCT imaging—were excluded. 4.Pregnant or breastfeeding women were excluded. 5.Patients with psychiatric disorders were excluded. 6.Patients with any contraindication that would preclude clinical evaluation or treatment were excluded. 7.Patients currently participating in other clinical trials were excluded. 8.Patients deemed unsuitable for study inclusion at the investigator’s discretion were excluded.

Design outcomes

Primary

MeasureTime frame
Central subfield thickness (CST);

Secondary

MeasureTime frame
Subretinal fluid;Ellipsoid zone disruption;

Countries

China

Contacts

Public ContactKun Liu

Shanghai General Hospital

drliukun@sjtu.edu.cn+86 21 63240090

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026