Study on the Biomarkers of Anti-VEGF Treatment for Choroidal Neovascularization
NCT ID: NCT06243406
Last Updated: 2024-02-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
80 participants
OBSERVATIONAL
2024-02-10
2024-10-31
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Interventions
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Intravitreal injection of anti-VEGF
Intravitreal injection of anti- vascular endothelial growth factor (VEGF) treatment
Eligibility Criteria
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Inclusion Criteria
* 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
* Any retinal diseases except choroidal neovascularization, such as multifocal choroiditis, diabetic retinopathy
* History of intraocular surgery
18 Years
90 Years
ALL
No
Sponsors
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Beijing Hospital
OTHER_GOV
Responsible Party
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Other Identifiers
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BJ-2022-012
Identifier Type: -
Identifier Source: org_study_id
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