Age Related Macular Degeneration Clinical Trial
Official title:
Observational Study to Evaluate and Compare the Rate and Extent of Inflammation After a Single Intravitreal Injection of Ranibizumab vs. a Single Intravitreal Injection of Aflibercept in Treatment Naive and Treatment Experienced Patients
This open-label, Phase IV prospective, observational study will evaluate patients, who have
been diagnosed with Neovascular Age-Related Macular Degeneration and have previously
received either a standard intravitreal injection of ranibizumab or aflibercept, in order to
get and compare information regarding post-injection inflammatory (irritation in the eye)2-3
days post-injection.
Additionally, patients will be evaluated for visual acuity and pain 2-3 days post-injection.
THIS IS AN OBSERVATION STUDY AND NOT AN INTERVENTIONAL STUDY AS TO ENTER THIS STUDY SUBJECTS
WILL HAVE HAD TO RECEIVED EITHER RANIBIZUMAB 0.5 MG OR AFIBERCEPT 2MG PRIOR TO ENTERING THE
STUDY AND SIGNING CONSENT. THIS STUDY IS TO OBSERVE THE SUBJECT POST-INJECTION RECEIVED
BEFORE ENTERING THIS STUDY.
Patients, age 65 to 90, with Neovascular Age-Related Macular Degeneration who present for treatment with intravitreal ranibizumab or aflibercept will be selected in this study. 300 subjects from one site in the United States will be enrolled. ;
Observational Model: Cohort, Time Perspective: Prospective
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