Actively Recruiting
Mecobalamin Combined With Anti-VEGF Intravitreal Injection for Retinal Vein Occlusion Treatment
Led by First Affiliated Hospital of Chongqing Medical University · Updated on 2026-02-27
120
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Retinal vein occlusion (RVO), a common retinal vascular disease, is frequently treated with anti-vascular endothelial growth factor (anti-VEGF) agents as first-line therapy. However, anti-VEGF monotherapy lacks neuroprotective effects, primarily targets vascular leakage and neovascularization, and requires frequent long-term injections that impose substantial economic burdens. Combined therapeutic strategies addressing both vascular pathology and neural damage are therefore being explored. This article describes the protocol for a randomized, outcome-blinded, placebo-controlled clinical trial evaluating mecobalamin (a widely used neuroprotective drug) in combination with anti-VEGF for the treatment of macular edema (ME). A total of 120 eligible RVO patients will be enrolled from the First Affiliated Hospital of Chongqing Medical University. Participants will be randomly assigned (1:1) to an experimental group and a control group. The experimental group will receive conventional anti-VEGF therapy plus oral mecobalamin capsules for 6 months, while the control group will receive the same anti-VEGF treatment plus a placebo for 6 months. All patients will undergo one year of follow-up after initial treatment, with visits at 1, 3, 6, 9, and 12 months. The primary outcome is the change in central subfield thickness (CST) from baseline to one year post-initial treatment. Secondary outcomes include: * Change in best-corrected visual acuity (BCVA) from baseline over time, * Capillary density, * Cone photoreceptor distribution characteristics, * Mean light sensitivity and fixation stability, * Serum vitamin B12 levels, * Number of anti-VEGF treatments, * Injection frequency (times per year), * Treatment interval, * Incidence and severity of adverse events (AEs) and serious adverse events (SAEs). This trial evaluates a novel "neuroprotection + vascular intervention" strategy combining mecobalamin with anti-VEGF therapy. The trial aims to provide high-level evidence for synergistic RVO treatment, with the potential to reduce recurrence rates and improve long-term visual function prognosis.
CONDITIONS
Official Title
Mecobalamin Combined With Anti-VEGF Intravitreal Injection for Retinal Vein Occlusion Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of retinal vein occlusion (RVO) meeting international diagnostic criteria
- Age between 18 and 80 years
- Any gender
- Treatment-naive RVO with macular edema (no prior anti-VEGF, glucocorticoid, or laser therapy)
- Central subfield thickness (CST) of 300 micrometers or more confirmed by optical coherence tomography (OCT)
- Baseline best-corrected visual acuity (BCVA) between 20/400 and 20/40 (34-78 ETDRS letters)
- Signed informed consent and ability to comply with study follow-up
You will not qualify if you...
- Other eye diseases causing macular edema such as diabetic retinopathy or uveitis
- Media opacities affecting imaging, including severe cataract or vitreous hemorrhage
- Prior anti-VEGF, steroid, or macular laser therapy
- Systemic use of glucocorticoids or immunosuppressants within the past 3 months
- Uncontrolled systemic diseases such as hypertension, diabetes, liver or kidney dysfunction
- Pregnant or lactating women
- Allergy to mecobalamin or conbercept
- Inability to cooperate with examinations or follow-up
- Participation in other clinical trials within one year
AI-Screening
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Trial Site Locations
Total: 1 location
1
No. 1, Friendship Road, Yuanjiagang, Yuzhong District, Chongqing City
Chongqing, China, 400016
Actively Recruiting
Research Team
W
Wen-Li Deng, doctoral
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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