Uncontrolled single site non randomized non interventional study to determine the safety and efficacy of intravitreal injections of Aflibercept in patients with recent vision loss due to retinal pigment epithelial detachment secondary to AMD
Study Type
OBSERVATIONAL
Enrollment
18
Patients are treated according to authorization of Aflibercept
University Hospital Muenster
Münster, Germany
Retention and improvement of visual acuity
Visual acuity after treatment completion compared to baseline
Time frame: Screening until 1 month after last injection within study eye (Month 12)
Height of Pigment Epithel Detachment
The height of PED after treatment completion compared to baseline
Time frame: Screening until 1 month after last injection within study eye (Month 12)
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