Actively Recruiting

Phase 4
Age: 18Years - 80Years
All Genders
NCT07133438

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

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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