Macular Degeneration Clinical Trial
Official title:
Macugen Observational Study
The objective of this observational study is to evaluate the effectiveness and safety of Macugen for treatment of wet age-related macular degeneration (AMD) in Indian patients.Prospective, Observational, Non-interventional Study. The period of observation for the study will be 1 year
To be eligible for enrollment in this study, patients must receive the first injection of
Macugen intravitreal in at least one eye for treatment of wet age-related macular
degeneration (AMD). The decision to prescribe Macugen will necessarily precede and will be
independent of the decision to enroll patient into the study.
If both eyes of a patient receive injection Macugen, only one eye will be included in the
study. If both eyes receive first injection Macugen after initiation of the study, only the
first treated eye will be included in the analysis. If one eye has already received Macugen
when the study starts and the second eye receives injection after the study initiation, the
second eye will be included in the analysis.
The study was prematurely discontinued due to delay in meeting pre-defined protocol
recruitment milestones on August 30, 2010. There were no safety concerns regarding the study
in the decision to terminate the trial.
;
Observational Model: Case-Only, Time Perspective: Prospective
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