Age Related Macular Degeneration Clinical Trial
Official title:
Time Course of Activity Signs at High Resolution OCT During OCT-guided High Frequency Intravitreal Ranibizumab Treatment in Choroidal Neovascularization Due to Age Related Macular Degeneration
The purpose of the study is to detect persisting or early new activity of choroidal neovascularization (CNV) due to age related macular degeneration (AMD) during the first 12 months following the first ranibizumab dose at baseline as assessed by weekly high resolution optical coherence tomography (OCT). Detection of persisting or new signs of CNV activity at OCT triggers further ranibizumab treatments considering that any ranibizumab injections can maximally be applied as often as 2-weekly.
This is a prospective, 1-arm, monocenter study designed to evaluate the time course of early
re-activation of CNV assessed by High Resolution OCT. An OCT-guided high frequency (up to
2-weekly) intravitreal ranibizumab treatment in CNV due to AMD may prevent further growth and
early re-growth of CNV as evaluated by OCT at a weekly basis.
Consenting, enrolled patients will receive one 0.5 mg ranibizumab intravitreal injection at
baseline (month 0). Afterwards all patients will undergo a weekly OCT assessment. Further
treatments, which can maximally be applied as often as 2-weekly, are triggered by persisting
or new signs of CNV activity at OCT as defined by intraretinal cysts or subretinal fluid. For
this study, a month is defined as 28 days, a 2-week period as 14 days. During the 12-month
study period, a maximum of 24 ranibizumab injections may be administered.
An interim analysis will not be performed. The study will be conducted in compliance with the
protocol, GCP and the applicable regulatory requirement(s).
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