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Study on the Treatment of Persistent DME with Poor Response to Non-Surgical Therapy through the Combination of Anti-VEGF Drugs and Epiretinal Membrane Peeling Surgery

Study on the Treatment of Persistent DME with Poor Response to Non-Surgical Therapy through the Combination of Anti-VEGF Drugs and Epiretinal Membrane Peeling Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098999
Enrollment
Unknown
Registered
2025-03-17
Start date
2024-03-24
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Diabetic macular edema

Interventions

Control group:Patients with persistent DME who do not respond to non-surgical treatment, in addition to conventional ophthalmic intraocular injection of anti-VEGF drugs (Conbercept) in combination wit
Experimental group:Patients with persistent DME who do not respond to non-surgical treatment, in addition to conventional ophthalmic intraocular injection of anti-VEGF drugs (Conbercept) in combinatio

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Retinal edema thickening in the area of 500 µm from the = fovea of the macula; with thickening of the adjacent retina; retinal thickening with at least 1 disk diameter (DD) range; 2. Age>=18 years; 3. The affected eye has received multiple anti-VEGF therapy in the past, but DME persists; or the macular foveal thickness is reduced by less than 50 µm; or the presence of epimacular membrane, showing signs of macula traction. However, the affected eye was not treated with any glass resection and macular surgery; 4. Voluntarily participate in this clinical trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with unclear diagnosis; 2. Patients who have had any intravitreal treatment or macular laser treatment or vitreoretinal surgery with steroids; 3. Patients with symptoms or manifestations that may be branch retinal vein occlusion; 4. Patients who refuse to participate in follow-up follow-up; 5. Those who participate in other clinical trials; 6. Any condition that, in the opinion of the investigator, needs to be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity;

Countries

China

Contacts

Public ContactJin XiaoLiang

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

xiaoliangjin80@163.com+86 186 2179 1056

Outcome results

None listed

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