Macular Degeneration Clinical Trial
Official title:
Efficacy of Ranibizumab Treatment Every 2 Month Compared to Treatment on Demand on Patients With Choroidal Neo-vascularization (CNV) as a Consequence of Age-related Macular Degeneration (AMD)
This clinical trial investigates the impact of intravitreal injection of Ranibizumab
antibody on the acuteness of vision. Patients included are suffering from choroidal
neo-vascularization (CNV) as a consequence of age-related macular degeneration (AMD).
Initially, all patients get injections of 0.5 mg Ranibizumab in monthly intervals for 3
months. Subsequently, one group gets Ranibizumab in intervals of 2 months, whereas a second
group is treated on demand.
The primary end point of the study is the change of best-corrected visual acuity after 12
month.
Secondary end points include the impact of Ranibizumab on morphological changes of the
retina, the number of patients with gain or loss of 15 or more letters visual acuity after
12 months, changes in quality of life and the number of injections required during the first
12 months of treatment.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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