42
Participants
Start Date
August 31, 2012
Primary Completion Date
April 30, 2016
Study Completion Date
April 30, 2016
PredA + Kelac
At week 12, patients will be determined to be resolved, improving/stabilized or treatment failures. Patients who have complete resolution of edema will begin treatment withdrawl. Improving/stabilizing patients will maintain current therapy. Treatment failure Group 2 patients will move to Group 3 to receive PredA q1h WA + Kelac qid starting at week 12. Treatment failure Group 1 patients will be exited from the trial so that alternative therapy can be given.
Wilmer Eye Institute, Baltimore
Johns Hopkins University
OTHER