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

B

Beijing Hospital

Status

Not yet enrolling

Conditions

Choroidal Neovascularization

Treatments

Other: Intravitreal injection of anti-VEGF

Study type

Observational

Funder types

Other

Identifiers

NCT06243406
BJ-2022-012

Details and patient eligibility

About

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.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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