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Observation of the efficacy of using different treatment regimens of Conbercept in the treatment of CRVO-ME in ethnic minority areas

Observation of the efficacy of using different treatment regimens of Conbercept in the treatment of CRVO-ME in ethnic minority areas

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107035
Enrollment
Unknown
Registered
2025-08-01
Start date
2025-08-05
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

retinal vein obstruction

Interventions

observation group:Anti-VEGF intravitreal injection:After 5 loading injections, a follow-up examination should be conducted once a month. If the condition remains stable, the interval for the next inje
control group:Anti-VEGF intravitreal injection:After completing five injections, have a follow-up checkup once a month. If the visual acuity drops by more than five letters or one line, or if the CST

Sponsors

Inner Mongolia Chaoyu Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with ME secondary to CRVO by OCT or FFA; 2. First treatment or no intraocular injection or retinal laser photocoagulation treatment within 3 months; 3.Age over 18 years old; 4.OCT examination results showed that the thickness of the macular fovea (CME) was > 250 µm; 5.Best corrected visual acuity between 0.05-0.5; 6.No traction in the macular area; 7.Complete follow-up data, and ; 8.Patients voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Previous eye diseases with cornea, lens, vitreous opacity and other refractive media affecting FFA, OCT and other examinations; 2.ME caused by other reasons;3. Previous internal eye surgery that seriously affects vision, such as after anti-glaucoma surgery, vitrectomy, etc;4.Previous glaucoma, retinal detachment, diabetic retinopathy and other eye diseases that seriously affect vision;5. Patients with severe. cardiovascular and cerebrovascular diseases and systemic diseases who cannot tolerate vitreous injection of conbercept;6.Patients with previous mental illness;7.CRVO secondary to neovascular glaucoma or iris neovascularization; 8.Those who are allergic to mydriatic drugs and local anesthetics; 9.Women who are preparing to give birth or are pregnant or lactating recently; 10. Patients with poor follow-up compliance.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity (BCVA);Macular foveal thickness (CMT);

Secondary

MeasureTime frame
The mean change in macular foveal thickness (CMT) compared to the baseline value;Number of injections;Mean change in best corrected visual acuity (BCVA) compared to baseline;

Countries

China

Contacts

Public ContactGuisen Zhang

Inner Mongolia Chaoyu Eye Hospital

zhangguisen76@sohu.com+86 189 0471 9852

Outcome results

None listed

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