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Mecobalamin combined with anti-VEGF intravitreal injection for treatment retinal vein occlusion: a double-blind randomized controlled trial

A randomized controlled trial of mecobalamin combined with anti-VEGF in the treatment of macular edema secondary to retinal vein occlusion (RVO-ME) : Multimodal dynamic assessment targeting the repair of retinal neurovascular units

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108682
Enrollment
Unknown
Registered
2025-09-03
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

retinal vein occlusion

Interventions

control group:placebo
Test group:Take mecobalamin capsules orally

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-80 years old, gender not limited; 2. diagnosed as macular edema secondary to monocular retinal vein occlusion (RVO-ME), and the CFT was confirmed to be >=300µm by OCT; 3. Newly diagnosed patients (who have not received anti-VEGF, glucocorticoid or laser treatment); 4. The baseline BCVA (ETDRS letter count) was 20/400 to 20/40 (34-78 letters); 5. Sign the informed consent form and be able to cooperate with the follow-up and examination;

Exclusion criteria

Exclusion criteria: 1. Combined with other eye diseases that cause macular edema (such as diabetic retinopathy, uveitis, glaucoma, etc.); 2. The presence of severe cataracts, vitreous hemorrhage or refractive medium opacity affects imaging examinations; 3. Systemic use of glucocorticoids or immunosuppressants within 3 months; 4. Severe systemic diseases; 5. allergic to mecobalamin or conbercept; 6. Pregnant or lactating women; 7. Inability to cooperate with examinations or follow-ups (such as mental illness, cognitive impairment); 8. Participate in other clinical trials within one year;

Design outcomes

Primary

MeasureTime frame
central foveal thickness;

Secondary

MeasureTime frame
Blood vitamin B12 content;Adverse Event (AE);The recurrence rate of macular edema within 12 months and the frequency of anti-VEGF injections;Changes in BCVA compared with the baseline;optical coherence tomography angiography;mfERG;Average light sensitivity of micro-field;

Countries

China

Contacts

Public ContactZhang Yanlai

The First Affiliated Hospital of Chongqing Medical University

zhangyanlai_666@163.com+86 23 8901 2011

Outcome results

None listed

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