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Study identifier: NCT02669953 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Aflibercept in Recurrent or Persistent CNV

Condition: Age Related Macular Degeneration · Intravitreal Injections · Diabetic Macular Edema  ·  Sponsor: Medical University of Vienna

PhaseN/A
Planned participants80
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

Age-related macular degeneration (AMD) and diabetic retinopathy are among the most common disorders causing visual disability in elderly people. AMD leads to dysfunction and loss of photoreceptors in the central retina. Neovascular AMD (nAMD) affects visual function early in the disease process. The purpose of the study is to evaluate the effect of switching from ranibizumab therapy to the current routine therapy using aflibercept in eyes with treatment naive, recurrent or persistent nAMD, treatment naive diabetic retinopathy and pretreated diabetic retinopathy. 20 patients with recurrent or persistent nAMD, previously treated with intravitreal ranibizumab for up to one year will be included in this trial. Patients will be examined in monthly intervals over 12 months follow-up. Examinations carried out will include: Best-corrected visual acuity (BCVA) using ETDRS charts at 4m distance, Reading Performance (RP), Standard ophthalmic examinations (SOE incl. funduscopy and applanation tonometry), Optical coherence tomography (OCT), Autofluorescence fundus image (AF) \& red-free autofluorescence fundus image (RF), Color fundus photography (CFP), Fluorescein angiography and indocyaningreen angiography (FLA/ICG), Microperimetry (MP), as well as Non-invasive OCT based optical angiography (AngioVue).

This description comes directly from the study's public registry record.

Talk to the study team

Reinhard Told, MD, PhD  ·  +43140400  ·  reinhard.told@meduniwien.ac.at

Stefan Sacu, Prof. PD. MD  ·  +43140400  ·  stefan.sacu@meduniwien.ac.at

Always discuss trial participation with your own doctor first.

Locations (1)

Medical University of ViennaVienna, AustriaRecruiting

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Source record: clinicaltrials.gov/study/NCT02669953