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Clinical Trials/KCT0007375
KCT0007375
Active, not recruiting
未知

The Effect of Intravitreal Aflibercept for Neovascular membrane, Pigment Epithelial Detachment and/or Subretinal Fluid Secondary to Type 1 Choroidal Neovascularization: Quantitative analysis based on OCT and OCT Angiography

Kyung Hee University Hospital0 sites40 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the eye and adnexa
Sponsor
Kyung Hee University Hospital
Enrollment
40
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Kyung Hee University Hospital

Eligibility Criteria

Inclusion Criteria

  • 1\. Active choroidal neovascularization confirmed by optical coherence tomography angiography or fluorescein angiography and indocyanine green angiography
  • \- When the subretinal fluid accompanied by irregular elevation of the retinal pigment epithelium is confirmed by optical coherence tomography
  • \- In cases where choroidal neovascularization is observed in optical coherence tomography angiography or fluorescein angiography and indocyanine green angiography
  • 2\. Male or female patients over 50 years of age who have signed the informed consent form
  • 3\. In the absence of active ocular or systemic disease
  • 4\. Patients who understand the process of this clinical trial, are cooperative, and are judged to be able to participate by the end of the clinical trial

Exclusion Criteria

  • 1\. Pregnant or lactating women
  • 2\. Patients participating in other clinical trials
  • 3\. If patient have received anti\-vascular endothelial growth factor treatment within the last 90 days
  • 4\. If patient have received photodynamic therapy 3 times or more or within the last 90 days
  • 5\. Clinically prominent diabetic retinopathy or diabetic macular edema
  • 6\. Clinically significant scar or atrophy of the fovea
  • 7\. Active Intraocular Inflammation or Infection
  • 8\. In case of hypersensitivity to Afilbercept and other ingredients in Eylea
  • 9\. History of intravitreal triamcinolone injection treatment within the last 3 months
  • 10\. History of intravitreal dexamethasone injection treatment within the last 6 months

Outcomes

Primary Outcomes

Not specified

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