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Conbercept for Retinal Vein Occlusion-Associated Macular Edema: Multi-Parameter Imaging Evaluation and Construction of AI-Assisted Prognostic Model

Conbercept for Retinal Vein Occlusion-Associated Macular Edema: Multi-Parameter Imaging Evaluation and Construction of AI-Assisted Prognostic Model

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122535
Enrollment
Unknown
Registered
2026-04-15
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Retinal Vein Occlusion Macular Edema

Interventions

Gold Standard:Gold Standard for Diagnosing RVO (BRVO/CRVO): Fluorescein Angiography (FFA) 1. Branch Retinal Vein Occlusion (BRVO) Tortuosity and dilation of a retinal vein Patchy hemorrhage and edema
Index test:Optical coherence tomography (OCT),?wide-field OCTA,?microperimeter

Sponsors

The Zhongshan Ophthalmic Center,Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years. 2.Diagnosis of RVO (BRVO or CRVO); 3.Macular edema (CST >=325 µm) involving the fovea, secondary to RVO. BCVA between 73 and 25 letters (ETDRS); 4.For patients who, owing to their medical condition, have determined to undergo Conbercept injection therapy, the informed consent form ought to be revised concurrently. 5.Those who have signed the informed consent;

Exclusion criteria

Exclusion criteria: 1.Active ocular inflammation or suspected/active ocular or periocular infection in either eye. 2.Concurrent vitreous hemorrhage, tractional retinal detachment, or epiretinal membrane involving the macular structure. 3.Uncontrolled glaucoma. 4.Any anti-VEGF therapy in the study eye within the preceding 3 months. 5.Any intravitreal (IVT), periocular, or implanted corticosteroid therapy, or use of any Iluvien® implant within the preceding 6 months. 6.Any cataract surgery within the preceding 3 months, or a history of other intraocular surgeries such as vitrectomy; 7.Individuals with mental illnesses or other medical conditions that prevent them from cooperating with surgery and follow-up; 8.Patients with poor communication skills and poor adherence; 9.Participate in other clinical trials;

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity (BCVA);

Secondary

MeasureTime frame
CST;MS;

Countries

China

Contacts

Public ContactXiling Yu

The Zhongshan Ophthalmic Center,Sun Yat-sen University

120736097@qq.com+86 20 6668 3995

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026