This is a one-year pilot, interventional, prospective, single arm, non-randomized, multicentric (3 centers) controlled study that aims to evaluate the response of type 3 choroidal neovascularization to treatment by Aflibercept following a classic protocol.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Poitiers University Hospital
Poitiers, France
Polyclinic of POITIERS
Poitiers, France
Mean change from baseline in Best Corrected Visual Acuity (BCVA)
Mean change from baseline in Best Corrected Visual Acuity (BCVA) as measured by ETDRS letter score at 4 meters
Time frame: 52 weeks
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