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Study on the Biomarkers of Anti-VEGF Treatment for Choroidal Neovascularization

Study on the Biomarkers to Predict the Response to Anti-vascular Endothelial Growth Factor Treatment for Choroidal Neovascularization

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06243406
Enrollment
80
Registered
2024-02-06
Start date
2024-02-10
Completion date
2024-10-31
Last updated
2024-02-07

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

Conditions

Choroidal Neovascularization

Brief summary

Choroidal neovascularization (CNV), also known as subretinal neovascularization, is a proliferative change from choroidal capillaries that has become one of the most important causes of blindness worldwide. CNV can occur in a variety of fundus diseases, including pathologic myopia, polypoidal choroidal vasculopathy. At present, intravitreal injection of anti-vascular endothelial growth factor (VEGF) drugs is the first-line effective treatment for CNV. Although a number of clinical studies have shown that the treatment of CNV with anti-VEGF drugs has achieved good visual and anatomical effects, there are still some patients whose CNV has not decreased significantly or even progressed continuously after treatment. Rapid advances in imaging technology have made it possible to explore the quantitative and qualitative characteristics of choroid and CNV, especially swept source optical coherence tomography angiography (SS-OCTA). The objectives are to improve the OCTA typing of CNV and analyze the vascular morphological characteristics of each type; to identify the changes in vascular characteristics of CNV after anti-VEGF treatment in vitreous cavity; and to elucidate the predictive effects of neovascularization and choroidal vascular characteristics on visual acuity and anatomic effects of vitreous anti-VEGF drug treatment for CNV.

Interventions

Intravitreal injection of anti- vascular endothelial growth factor (VEGF) treatment

Sponsors

Beijing Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years

Inclusion criteria

* Age \>18 years old * Active choroidal neovascularization (activity criteria: blood vessel leakage confirmed by FFA, or subretinal fluid accumulation or bleeding seen by OCT) * History of anti-VEGF drug therapy * At least 3 months of follow-up data.

Exclusion criteria

* Unable to complete the examination due to severe cataract or vitreous hemorrhage * Any retinal diseases except choroidal neovascularization, such as multifocal choroiditis, diabetic retinopathy * History of intraocular surgery

Design outcomes

Primary

MeasureTime frameDescription
choroidal thickness3 monthscentral choroidal thickness measured by SS-OCTA
Central retinal thickness3 monthscentral retinal thickness changes measured by SS-OCTA
Best-corrected visual acuity3 monthsBest-corrected visual acuity changes from baseline to 3 months

Secondary

MeasureTime frameDescription
choroidal vascularity index3 monthsthe ratio of vascular area to the total choroidal area measured by SS-OCTA

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026