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Intravitreal Injection of Conbercept for Macular Edema due to Branch Retinal Vein Occlusion: the Efficacy Analysis of Early versus Late

Intravitreal Injection of Conbercept for Macular Edema due to Branch Retinal Vein Occlusion: the Efficacy Analysis of Early versus Late

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018245
Enrollment
Unknown
Registered
2018-09-06
Start date
2018-10-01
Completion date
Unknown
Last updated
2018-09-10

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

Conditions

Branch Retinal Vein Occlusion

Interventions

patients with macular edema secondary to branch retinal vein occlusion within 90 days of CME onset:intravitreal Conbercept injection
patients with macular edema secondary to branch retinal vein occlusion after 90 days of CME onset:intravitreal Conbercept injection

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients =18 years old with central macular edema secondary to BRVO diagnosed by OCT and FFA within 12 months, and the study eyes BCVA between 19 and 73 Early Treatment Diabetic Retinopathy Study (ETDRS) letters (20/400 and 20/40 Snellen equivalent), and the other eyes BCVA was >34 ETDRS (>20/200Snellen equivalent). Only one eye from each patient was included in this study.

Exclusion criteria

Exclusion criteria: The exclusion criteria included ocular or general use of other test drugs, systemic steroids within the last 6 months for at least 30 days, intraocular or periocular steroid treatment in the study eye within the last 3 months, eyes with history of treatment that could potentially affect the study, including intraocular laser, and vitrectomy, combined other ocular or systemic problems included ocular inflammation in both eyes, uncontrolled glaucoma, myocardial infarction, and uncontrolled hypertension, et.al.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity;central foveal thickness;

Countries

China

Contacts

Public ContactWENJUAN LUO

Affiliated Hospital of Qingdao University

Luowj76@163.com+86 17853298800

Outcome results

None listed

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